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You searched for subject:(Anticancer agents). Showing records 1 – 30 of 72 total matches.

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Wake Forest University

1. Pickard, Amanda Jayne. NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS.

Degree: 2014, Wake Forest University

 Traditional DNA-targeted anticancer agents, such as platinum-based therapies, have been a mainstay in the treatment of aggressive solid malignancies in the clinical setting. Unfortunately, due… (more)

Subjects/Keywords: Anticancer agents

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APA (6th Edition):

Pickard, A. J. (2014). NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/39394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pickard, Amanda Jayne. “NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS.” 2014. Thesis, Wake Forest University. Accessed January 15, 2021. http://hdl.handle.net/10339/39394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pickard, Amanda Jayne. “NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS.” 2014. Web. 15 Jan 2021.

Vancouver:

Pickard AJ. NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS. [Internet] [Thesis]. Wake Forest University; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10339/39394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pickard AJ. NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS. [Thesis]. Wake Forest University; 2014. Available from: http://hdl.handle.net/10339/39394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Baylor University

2. George, Clinton S. Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents.

Degree: PhD, Chemistry and Biochemistry., 2012, Baylor University

 Targeting the vascular network that supplies a tumor with oxygen and nutrients is a viable methodology for the treatment of cancer. With the discovery of… (more)

Subjects/Keywords: Anticancer agents.

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APA (6th Edition):

George, C. S. (2012). Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents. (Doctoral Dissertation). Baylor University. Retrieved from http://hdl.handle.net/2104/8482

Chicago Manual of Style (16th Edition):

George, Clinton S. “Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents.” 2012. Doctoral Dissertation, Baylor University. Accessed January 15, 2021. http://hdl.handle.net/2104/8482.

MLA Handbook (7th Edition):

George, Clinton S. “Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents.” 2012. Web. 15 Jan 2021.

Vancouver:

George CS. Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents. [Internet] [Doctoral dissertation]. Baylor University; 2012. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2104/8482.

Council of Science Editors:

George CS. Targeting the tumor microenvironment through the design and synthesis of potent, small-molecule, anticancer agents. [Doctoral Dissertation]. Baylor University; 2012. Available from: http://hdl.handle.net/2104/8482

3. Pandita, Renu Moti. SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No.

Degree: Sciences, 2014, Guru Nanak Dev University

newline No

Summary:137-150, References:151-166

Advisors/Committee Members: Saxena, A.K..

Subjects/Keywords: ANTICANCER AGENTS

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APA (6th Edition):

Pandita, R. M. (2014). SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/23708

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pandita, Renu Moti. “SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No.” 2014. Thesis, Guru Nanak Dev University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/23708.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pandita, Renu Moti. “SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No.” 2014. Web. 15 Jan 2021.

Vancouver:

Pandita RM. SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/23708.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pandita RM. SOME POTENTIAL ANTICANCER AGENTS FROM PLANTS WITH SPECIAL EMPHASIS ON ACACIA NILOTICA NARDOSTACHYS JATAMANSI AND CRYPTOLEPIS BUCHANANI; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/23708

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Stony Brook University

4. Chen, Guan-Ting. Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents .

Degree: 2009, Stony Brook University

Subjects/Keywords: Anticancer agents

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APA (6th Edition):

Chen, G. (2009). Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents . (Thesis). Stony Brook University. Retrieved from http://hdl.handle.net/1951/52209

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chen, Guan-Ting. “Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents .” 2009. Thesis, Stony Brook University. Accessed January 15, 2021. http://hdl.handle.net/1951/52209.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chen, Guan-Ting. “Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents .” 2009. Web. 15 Jan 2021.

Vancouver:

Chen G. Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents . [Internet] [Thesis]. Stony Brook University; 2009. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1951/52209.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chen G. Synthetic Studies on Difluorovinyl-Taxoid Anticancer Agents and Benzimidazole-Based Antituberculosis Agents . [Thesis]. Stony Brook University; 2009. Available from: http://hdl.handle.net/1951/52209

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of New South Wales

5. Gorle, Anil Kumar. Polypyridylruthenium(II) complexes as therapeutic agents.

Degree: Physical, Environmental & Mathematical Sciences, 2015, University of New South Wales

 A series of dinuclear ruthenium(II) complexes containing labile chlorido ligands (Cl-Rubbn) have been synthesised and their potential as anticancer agents examined. Some of the Cl-Rubbn… (more)

Subjects/Keywords: antimicrobial agents; Polypyridylruthenium(II) complexes; Therapeutic agents; anticancer agents

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APA (6th Edition):

Gorle, A. K. (2015). Polypyridylruthenium(II) complexes as therapeutic agents. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55233 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36838/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Gorle, Anil Kumar. “Polypyridylruthenium(II) complexes as therapeutic agents.” 2015. Doctoral Dissertation, University of New South Wales. Accessed January 15, 2021. http://handle.unsw.edu.au/1959.4/55233 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36838/SOURCE02?view=true.

MLA Handbook (7th Edition):

Gorle, Anil Kumar. “Polypyridylruthenium(II) complexes as therapeutic agents.” 2015. Web. 15 Jan 2021.

Vancouver:

Gorle AK. Polypyridylruthenium(II) complexes as therapeutic agents. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 Jan 15]. Available from: http://handle.unsw.edu.au/1959.4/55233 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36838/SOURCE02?view=true.

Council of Science Editors:

Gorle AK. Polypyridylruthenium(II) complexes as therapeutic agents. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55233 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36838/SOURCE02?view=true

6. Bhagat, Madhulika. SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No.

Degree: Science, 2014, Guru Nanak Dev University

newline No

Summary:63-174 references:175-191, list of publication : 192

Advisors/Committee Members: SAXENA, A.K..

Subjects/Keywords: ANTICANCER AGENTS; PLANTS

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APA (6th Edition):

Bhagat, M. (2014). SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/32056

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bhagat, Madhulika. “SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No.” 2014. Thesis, Guru Nanak Dev University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/32056.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bhagat, Madhulika. “SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No.” 2014. Web. 15 Jan 2021.

Vancouver:

Bhagat M. SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32056.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bhagat M. SEARCH FOR POTENTIAL ANTICANCER AGENTS FROM PLANTS; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32056

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

7. Ma, Zhidong. STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER.

Degree: 2009, Wake Forest University

 DNA-directed chemotherapies continue to play an important role in modern oncology. The cytotoxic complex, [PtCl(en)(ACRAMTU)](NO3)2 (en = ethane-1,2-diamine; ACRAMTU = 1-[2-(acridine-9-ylamino)ethyl]-1,3-dimethylthiourea) (PT-ACRAMTU, 31), is a… (more)

Subjects/Keywords: Anticancer agents

…x5D;. It is then understandable that in the development of cytotoxic anticancer agents… …agents and their molecular interaction with DNA. Figure 4. 3 6 Ethidium, doxorubicin and… …development of N-mustard-based cytotoxic agents. 13 X Figure 10. Monoalkylation and cross… …linking chemistry of alkylating agents. 14 Figure 11. Structure of bleomycin. Figure 12. DNA… …Agents for the Treatment of Non-Small-Cell Lung Cancer By Zhidong Ma Dissertation under the… 

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APA (6th Edition):

Ma, Z. (2009). STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/14816

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ma, Zhidong. “STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER.” 2009. Thesis, Wake Forest University. Accessed January 15, 2021. http://hdl.handle.net/10339/14816.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ma, Zhidong. “STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER.” 2009. Web. 15 Jan 2021.

Vancouver:

Ma Z. STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER. [Internet] [Thesis]. Wake Forest University; 2009. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10339/14816.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ma Z. STRUCTURE–ACTIVITY RELATIONSHIP STUDIES OF HYBRID ANTITUMOR AGENTS FOR THE TREATMENT OF NON-SMALL CELL LUNG CANCER. [Thesis]. Wake Forest University; 2009. Available from: http://hdl.handle.net/10339/14816

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Rice University

8. Yu, Ruocheng. Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units.

Degree: PhD, Natural Sciences, 2017, Rice University

 The prostaglandins (PGs) are a class of natural products that have enjoyed unparalleled popularity among the chemical and biological community over the past century. The… (more)

Subjects/Keywords: total synthesis; anticancer agents; prostaglandin; tropolone

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APA (6th Edition):

Yu, R. (2017). Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105591

Chicago Manual of Style (16th Edition):

Yu, Ruocheng. “Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units.” 2017. Doctoral Dissertation, Rice University. Accessed January 15, 2021. http://hdl.handle.net/1911/105591.

MLA Handbook (7th Edition):

Yu, Ruocheng. “Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units.” 2017. Web. 15 Jan 2021.

Vancouver:

Yu R. Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units. [Internet] [Doctoral dissertation]. Rice University; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1911/105591.

Council of Science Editors:

Yu R. Synthesis of anticancer agents: 15-deoxy-15-fluoro-Δ12-prostaglandin J3 and gukulenin monomeric units. [Doctoral Dissertation]. Rice University; 2017. Available from: http://hdl.handle.net/1911/105591

9. Sanchez, Clément. Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D.

Degree: Docteur es, Ingénierie biomoléculaire, 2016, Montpellier

La Cathepsine D (CathD) est une protéase lysosomale surexprimée et sécrétée par de nombreuses tumeurs solides. Cette enzyme favorise la prolifération tumorale et le processus… (more)

Subjects/Keywords: Vectorisation; Cathepsine D; Agents anticancéreux; Vectorization; Cathepsin D; Anticancer agents

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APA (6th Edition):

Sanchez, C. (2016). Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2016MONTS001

Chicago Manual of Style (16th Edition):

Sanchez, Clément. “Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D.” 2016. Doctoral Dissertation, Montpellier. Accessed January 15, 2021. http://www.theses.fr/2016MONTS001.

MLA Handbook (7th Edition):

Sanchez, Clément. “Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D.” 2016. Web. 15 Jan 2021.

Vancouver:

Sanchez C. Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D. [Internet] [Doctoral dissertation]. Montpellier; 2016. [cited 2021 Jan 15]. Available from: http://www.theses.fr/2016MONTS001.

Council of Science Editors:

Sanchez C. Développement de vecteurs de pénétration intracellulaire pour un adressage d’inhibiteurs de la cathepsine D : Development of cell penetration vectors for addressing inhibitors of cathepsin D. [Doctoral Dissertation]. Montpellier; 2016. Available from: http://www.theses.fr/2016MONTS001


Universiteit Utrecht

10. Vainchtein, L.D. Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents.

Degree: 2008, Universiteit Utrecht

 To understand the pharmacologic mechanisms of action, efficacy and toxicity of any anti-cancer drug it is important to know how the compound is transformed in… (more)

Subjects/Keywords: Farmacie; mass spectrometry; liquid chromatography; anticancer agents; metabolites

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APA (6th Edition):

Vainchtein, L. D. (2008). Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/26273

Chicago Manual of Style (16th Edition):

Vainchtein, L D. “Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/26273.

MLA Handbook (7th Edition):

Vainchtein, L D. “Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents.” 2008. Web. 15 Jan 2021.

Vancouver:

Vainchtein LD. Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/26273.

Council of Science Editors:

Vainchtein LD. Liquid Chromatography - Triple Quadrupole Mass Spectrometry : The gold standard for quantitative bioanalysis of anti-cancer agents. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/26273


Universiteit Utrecht

11. Brouwers, E.E.M. Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents.

Degree: 2007, Universiteit Utrecht

 After the discovery of the antiproliferative effects of cisplatin, the drug has developed into one of the most frequently used anticancer agents. Unfortunately, the use… (more)

Subjects/Keywords: Farmacie; ICP-MS; oncology; metal-based anticancer agents; platinum; ruthenium

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APA (6th Edition):

Brouwers, E. E. M. (2007). Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/23762

Chicago Manual of Style (16th Edition):

Brouwers, E E M. “Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/23762.

MLA Handbook (7th Edition):

Brouwers, E E M. “Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents.” 2007. Web. 15 Jan 2021.

Vancouver:

Brouwers EEM. Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/23762.

Council of Science Editors:

Brouwers EEM. Inductively coupled plasma mass spectrometry: a unique, ultrasensitive tool for exploring the pharmacology of metal-based anticancer agents. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/23762


Universiteit Utrecht

12. Nijenhuis, Cynthia Marcella. Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies.

Degree: 2016, Universiteit Utrecht

 Cancer is already among the leading causes of death worldwide and the number of new cases is expected to rise by about 70% over the… (more)

Subjects/Keywords: clinical pharmacology; pharmacokinetics; mass balance studies; anticancer agents; bioanalysis

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APA (6th Edition):

Nijenhuis, C. M. (2016). Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/338039

Chicago Manual of Style (16th Edition):

Nijenhuis, Cynthia Marcella. “Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/338039.

MLA Handbook (7th Edition):

Nijenhuis, Cynthia Marcella. “Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies.” 2016. Web. 15 Jan 2021.

Vancouver:

Nijenhuis CM. Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/338039.

Council of Science Editors:

Nijenhuis CM. Clinical pharmacology of novel anticancer agents: bioanalysis - clinical pharmacokinetics - mass balance studies. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/338039

13. Akhtar, Salman. Molecular modeling studies of the selected anticancer agents and their structural analogs;.

Degree: Bioinformatics, 2014, Integral University

None

Reference included in chapters

Advisors/Committee Members: Jamal M Arif.

Subjects/Keywords: Bioinformatics; Anticancer agents; Molecular modeling

Page 1

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APA (6th Edition):

Akhtar, S. (2014). Molecular modeling studies of the selected anticancer agents and their structural analogs;. (Thesis). Integral University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/16277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Akhtar, Salman. “Molecular modeling studies of the selected anticancer agents and their structural analogs;.” 2014. Thesis, Integral University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/16277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Akhtar, Salman. “Molecular modeling studies of the selected anticancer agents and their structural analogs;.” 2014. Web. 15 Jan 2021.

Vancouver:

Akhtar S. Molecular modeling studies of the selected anticancer agents and their structural analogs;. [Internet] [Thesis]. Integral University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Akhtar S. Molecular modeling studies of the selected anticancer agents and their structural analogs;. [Thesis]. Integral University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

14. Matinder Kaur. DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No.

Degree: Science, 2014, Guru Nanak Dev University

No newline

Summary:140-151, List of Publication on last pages

Advisors/Committee Members: Palwinder Singh.

Subjects/Keywords: CONJUGATES; ORGANIC MOLECULES; ANTICANCER AGENTS

Page 1 Page 2

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APA (6th Edition):

Kaur, M. (2014). DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29765

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kaur, Matinder. “DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No.” 2014. Thesis, Guru Nanak Dev University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/29765.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kaur, Matinder. “DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No.” 2014. Web. 15 Jan 2021.

Vancouver:

Kaur M. DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29765.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kaur M. DESIGN SYNTHESIS AND DEVELOPMENT OF CONJUGATES OF SMALL ORGANIC MOLECULES AS ANTICANCER AGENTS AND MULTIDRUG RESISTANCE MODULATORS; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29765

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

15. Bhagat, Madhulika. Search for potential anticancer agents from plants;.

Degree: Molecular biology, 2014, Guru Nanak Dev University

None

Summary p. 63-174, References p. 175-191, List of publication p. 192

Advisors/Committee Members: Saxena, A K.

Subjects/Keywords: Molecular biology; Anticancer agents

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APA (6th Edition):

Bhagat, M. (2014). Search for potential anticancer agents from plants;. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/20791

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bhagat, Madhulika. “Search for potential anticancer agents from plants;.” 2014. Thesis, Guru Nanak Dev University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/20791.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bhagat, Madhulika. “Search for potential anticancer agents from plants;.” 2014. Web. 15 Jan 2021.

Vancouver:

Bhagat M. Search for potential anticancer agents from plants;. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/20791.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bhagat M. Search for potential anticancer agents from plants;. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/20791

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Soepenberg, Otto. Prolonging the exposure to anti-cancer agents.

Degree: Department of Medical Oncology, 2004, Erasmus University Medical Center

 textabstractThis thesis includes phase I clinical and pharmacological studies on second and third generation topoisomerase I inhibitors, either administered orally, or intravenously as a macromolecular… (more)

Subjects/Keywords: pharmacokinetics; treatment; paclitaxel; anticancer agents

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APA (6th Edition):

Soepenberg, O. (2004). Prolonging the exposure to anti-cancer agents. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/51512

Chicago Manual of Style (16th Edition):

Soepenberg, Otto. “Prolonging the exposure to anti-cancer agents.” 2004. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 15, 2021. http://hdl.handle.net/1765/51512.

MLA Handbook (7th Edition):

Soepenberg, Otto. “Prolonging the exposure to anti-cancer agents.” 2004. Web. 15 Jan 2021.

Vancouver:

Soepenberg O. Prolonging the exposure to anti-cancer agents. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2004. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1765/51512.

Council of Science Editors:

Soepenberg O. Prolonging the exposure to anti-cancer agents. [Doctoral Dissertation]. Erasmus University Medical Center; 2004. Available from: http://hdl.handle.net/1765/51512


Loughborough University

17. Aldabbagh, Fawaz. Radical cyclisations onto imidazoles.

Degree: PhD, 1997, Loughborough University

 This thesis describes the development of new pathways towards the synthesis of novel antimicrobial (and anticancer) agents. Two synthetic protocols based on free radical chemistry… (more)

Subjects/Keywords: 547; Pyrrole; Antimicrobial agents; Anticancer

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APA (6th Edition):

Aldabbagh, F. (1997). Radical cyclisations onto imidazoles. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/32471

Chicago Manual of Style (16th Edition):

Aldabbagh, Fawaz. “Radical cyclisations onto imidazoles.” 1997. Doctoral Dissertation, Loughborough University. Accessed January 15, 2021. http://hdl.handle.net/2134/32471.

MLA Handbook (7th Edition):

Aldabbagh, Fawaz. “Radical cyclisations onto imidazoles.” 1997. Web. 15 Jan 2021.

Vancouver:

Aldabbagh F. Radical cyclisations onto imidazoles. [Internet] [Doctoral dissertation]. Loughborough University; 1997. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2134/32471.

Council of Science Editors:

Aldabbagh F. Radical cyclisations onto imidazoles. [Doctoral Dissertation]. Loughborough University; 1997. Available from: http://hdl.handle.net/2134/32471


University of Cincinnati

18. Abdul Salam, Safnas Farwin. Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells.

Degree: PhD, Arts and Sciences: Chemistry, 2017, University of Cincinnati

 Reactive oxygen species (ROS), includes highly reactive molecules and radicals, derived from metabolism of molecular oxygen, and have important roles in cellular signaling. At high… (more)

Subjects/Keywords: Biochemistry; ROS; Anticancer agents; antioxidant; oxidative stress; DNA damage; oxazolone

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APA (6th Edition):

Abdul Salam, S. F. (2017). Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511880706270521

Chicago Manual of Style (16th Edition):

Abdul Salam, Safnas Farwin. “Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells.” 2017. Doctoral Dissertation, University of Cincinnati. Accessed January 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511880706270521.

MLA Handbook (7th Edition):

Abdul Salam, Safnas Farwin. “Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells.” 2017. Web. 15 Jan 2021.

Vancouver:

Abdul Salam SF. Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2017. [cited 2021 Jan 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511880706270521.

Council of Science Editors:

Abdul Salam SF. Biochemistry of Reactive Oxygen Species in Selective Cancer Cell Toxicity and Protection of Normal Cells. [Doctoral Dissertation]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511880706270521


University of New South Wales

19. Pisani, Michelle. Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs.

Degree: Physical, 2011, University of New South Wales

 This thesis reports the development of a series of inert dinuclear polypyridylruthenium(II) complexes from DNA binding agents to anticancer drugs. The complexes of the general… (more)

Subjects/Keywords: DNA-binding affinity; Molecular modelling; Cytotoxicity; Anticancer agents; Cellular uptake

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APA (6th Edition):

Pisani, M. (2011). Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52123 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10793/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Pisani, Michelle. “Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs.” 2011. Doctoral Dissertation, University of New South Wales. Accessed January 15, 2021. http://handle.unsw.edu.au/1959.4/52123 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10793/SOURCE01?view=true.

MLA Handbook (7th Edition):

Pisani, Michelle. “Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs.” 2011. Web. 15 Jan 2021.

Vancouver:

Pisani M. Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2021 Jan 15]. Available from: http://handle.unsw.edu.au/1959.4/52123 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10793/SOURCE01?view=true.

Council of Science Editors:

Pisani M. Inert Dinuclear Polypyridylruthenium (II) Complexes as Anticancer Drugs. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/52123 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10793/SOURCE01?view=true


Indian Institute of Science

20. Ali, Asfa. New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 The thesis entitled “New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production” encompasses design, computational calculations, and… (more)

Subjects/Keywords: DNA Targeted Samll Molecules; DNA Binding Small Molecules Anticancer Agents; DNA Binding Anticancer Drugs; G-Quadruplex DNA; Oligopyrrole Carboxamides; DNA Targeting Cancer Drugs; Anticancer Drugs; Bombyx Mori Gene Expression; Molecular Targeted Anticancer Agents; Organic Chemistry

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APA (6th Edition):

Ali, A. (2018). New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3514

Chicago Manual of Style (16th Edition):

Ali, Asfa. “New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed January 15, 2021. http://etd.iisc.ac.in/handle/2005/3514.

MLA Handbook (7th Edition):

Ali, Asfa. “New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production.” 2018. Web. 15 Jan 2021.

Vancouver:

Ali A. New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Jan 15]. Available from: http://etd.iisc.ac.in/handle/2005/3514.

Council of Science Editors:

Ali A. New DNA-Targeting Small Molecules as Potential Anticancer Agents and for in vivo Specificity toward Enhanced Silk Production. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3514


University of California – San Diego

21. Rhoades, Derek. Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A.

Degree: Chemistry, 2016, University of California – San Diego

 The epothilones are an intriguing class of natural products and a classic in total synthesis. Their remarkable biological properties have been under investigation for the… (more)

Subjects/Keywords: Organic chemistry; Anticancer Agents; Medicinal Chemistry; Molecular Design; Natural Products; Organic Synthesis

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APA (6th Edition):

Rhoades, D. (2016). Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/5h39h8j1

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rhoades, Derek. “Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A.” 2016. Thesis, University of California – San Diego. Accessed January 15, 2021. http://www.escholarship.org/uc/item/5h39h8j1.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rhoades, Derek. “Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A.” 2016. Web. 15 Jan 2021.

Vancouver:

Rhoades D. Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2021 Jan 15]. Available from: http://www.escholarship.org/uc/item/5h39h8j1.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rhoades D. Synthesis of Natural and Designed Antitumor Agents: Epothilones and Thailanstatin A. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/5h39h8j1

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – San Diego

22. Hoong, Christina. Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents.

Degree: Chemistry, 2017, University of California – San Diego

 Since the discovery of ferrocene in 1951 and subsequent structure elucidation in the following years, a wealth of literature is available on ferrocene functionalization. The… (more)

Subjects/Keywords: Organic chemistry; anticancer; benzoyl ferrocene derivatives; ferrocenyl agents; ferroptosis; iron homeostasis; small molecule synthesis

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APA (6th Edition):

Hoong, C. (2017). Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4dk1c7nz

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hoong, Christina. “Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents.” 2017. Thesis, University of California – San Diego. Accessed January 15, 2021. http://www.escholarship.org/uc/item/4dk1c7nz.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hoong, Christina. “Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents.” 2017. Web. 15 Jan 2021.

Vancouver:

Hoong C. Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2021 Jan 15]. Available from: http://www.escholarship.org/uc/item/4dk1c7nz.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hoong C. Synthesis, Design, and Cytotoxicity of Organoferrous Anticancer Agents. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/4dk1c7nz

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. Sharma, Madhunika. Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No.

Degree: Sciences, 2014, Guru Nanak Dev University

No newline

Summary:77-82, References:83-106, Credentials: 107

Advisors/Committee Members: Saxena, A.K..

Subjects/Keywords: Anticancer Agents; Ocimum viride Ocimum carnosum

Page 1

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APA (6th Edition):

Sharma, M. (2014). Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29784

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sharma, Madhunika. “Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No.” 2014. Thesis, Guru Nanak Dev University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/29784.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sharma, Madhunika. “Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No.” 2014. Web. 15 Jan 2021.

Vancouver:

Sharma M. Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29784.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sharma M. Studies on Anticancer Agents from Ocimum viride Ocimum carnosum and Vallaris solanacea; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29784

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Bradford

24. Elbakay, Jamal Ali Mohamed. Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics.

Degree: PhD, 2017, University of Bradford

 Methotrexate (MTX) is an antimetabolite anticancer agent that is used in treatment of multiple cancers, such as acute lymphoblastic leukaemia and osteosarcoma. A lack of… (more)

Subjects/Keywords: 616.99; Cancer; Prodrug; Methotrexate; HDMTX; Matrix Metalloproteinase (MMP); Peptide; Anticancer agents; Methotrexate (MTX)

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APA (6th Edition):

Elbakay, J. A. M. (2017). Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/15102

Chicago Manual of Style (16th Edition):

Elbakay, Jamal Ali Mohamed. “Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics.” 2017. Doctoral Dissertation, University of Bradford. Accessed January 15, 2021. http://hdl.handle.net/10454/15102.

MLA Handbook (7th Edition):

Elbakay, Jamal Ali Mohamed. “Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics.” 2017. Web. 15 Jan 2021.

Vancouver:

Elbakay JAM. Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics. [Internet] [Doctoral dissertation]. University of Bradford; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10454/15102.

Council of Science Editors:

Elbakay JAM. Synthesis and pharmacological evaluation of novel anti-tumour prodrugs : synthesis and pharmacological investigations into novel MMP-activated peptide-based prodrugs of methotrexate as potential cancer therapeutics. [Doctoral Dissertation]. University of Bradford; 2017. Available from: http://hdl.handle.net/10454/15102


Université de Grenoble

25. Genoux, Estelle. Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity.

Degree: Docteur es, Chimie biologie, 2011, Université de Grenoble

La résistance aux agents chimiothérapeutiques (Multidrug Resistance ou MDR) est caractérisée par la surexpression de différentes protéines membranaires de type ABC, parmi lesquelles, MRP1 et… (more)

Subjects/Keywords: Flavonoïdes; Pharmacomodulation; Anticancéreux; MRP1; BCRP; Flavonoids; Pharmacomodulation; Anticancer agents; Modulators; MRP1; BCRP; 540; 570

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APA (6th Edition):

Genoux, E. (2011). Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2011GRENV015

Chicago Manual of Style (16th Edition):

Genoux, Estelle. “Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity.” 2011. Doctoral Dissertation, Université de Grenoble. Accessed January 15, 2021. http://www.theses.fr/2011GRENV015.

MLA Handbook (7th Edition):

Genoux, Estelle. “Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity.” 2011. Web. 15 Jan 2021.

Vancouver:

Genoux E. Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity. [Internet] [Doctoral dissertation]. Université de Grenoble; 2011. [cited 2021 Jan 15]. Available from: http://www.theses.fr/2011GRENV015.

Council of Science Editors:

Genoux E. Dérivés de flavonoïdes et de vérapamil comme ligands des transporteurs MRP1 et ABCG2 : de la conception à l'activité anticancéreuse : Derivatives of flavonoids and verapamil as ligands of MRP1 and ABCG2 transporters : from design to anticancer activity. [Doctoral Dissertation]. Université de Grenoble; 2011. Available from: http://www.theses.fr/2011GRENV015

26. Cheung-Ong, Kahlin. Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics.

Degree: 2013, University of Toronto

Chemotherapeutic agents act by targeting rapidly dividing cancer cells. The full extent of their cellular mechanisms, which is essential to balance efficacy and toxicity, is… (more)

Subjects/Keywords: Chemical Genomics; Anticancer Agents; 0307

…alkylating-like platinum agents had a significant positive impact on anticancer drug research. The… …105 ix List of Figures Figure 1-1. Structures of selected DNA-damaging anticancer… …and Nislow C. (2013) DNA-Damaging Agents in Cancer Chemotherapy: Serendipity and… …Chemical Biology. Chem Biol. In press. 1.1 Cancer chemotherapy 1.1.1 DNA-damaging agents as… …antifolates had potential as anticancer compounds. Another folate analogue with less toxicity than… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cheung-Ong, K. (2013). Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35790

Chicago Manual of Style (16th Edition):

Cheung-Ong, Kahlin. “Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics.” 2013. Doctoral Dissertation, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/35790.

MLA Handbook (7th Edition):

Cheung-Ong, Kahlin. “Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics.” 2013. Web. 15 Jan 2021.

Vancouver:

Cheung-Ong K. Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/35790.

Council of Science Editors:

Cheung-Ong K. Development and Application of High-throughput Chemical Genomic Screens for Functional Studies of Cancer Therapeutics. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35790


University of Melbourne

27. Goh, Sook Jin. Synthesis and characterizations of anticancer amphiphilic star polypeptides.

Degree: 2017, University of Melbourne

 The cancer had replaced infectious diseases as the second major leading cause of deaths globally in 2013. Currently, chemotherapy is the main treatment option for… (more)

Subjects/Keywords: amphiphilic polypeptide; anticancer agents; N-carboxyanhydride ring-opening polymerization (NCA-ROP); alpha-helix

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APA (6th Edition):

Goh, S. J. (2017). Synthesis and characterizations of anticancer amphiphilic star polypeptides. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/210469

Chicago Manual of Style (16th Edition):

Goh, Sook Jin. “Synthesis and characterizations of anticancer amphiphilic star polypeptides.” 2017. Masters Thesis, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/210469.

MLA Handbook (7th Edition):

Goh, Sook Jin. “Synthesis and characterizations of anticancer amphiphilic star polypeptides.” 2017. Web. 15 Jan 2021.

Vancouver:

Goh SJ. Synthesis and characterizations of anticancer amphiphilic star polypeptides. [Internet] [Masters thesis]. University of Melbourne; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/210469.

Council of Science Editors:

Goh SJ. Synthesis and characterizations of anticancer amphiphilic star polypeptides. [Masters Thesis]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/210469


Mahatma Gandhi University

28. Jacob, Lijy. Anticancer studies of Clitoria ternatea Linn;.

Degree: Biochemistry, 2014, Mahatma Gandhi University

newline

Bibliography p. 222-256

Advisors/Committee Members: Latha, M S.

Subjects/Keywords: Anticancer agents; Antineoplastic agents; Carcinogens; Clitoria ternatea (Linn)

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APA (6th Edition):

Jacob, L. (2014). Anticancer studies of Clitoria ternatea Linn;. (Thesis). Mahatma Gandhi University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25741

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jacob, Lijy. “Anticancer studies of Clitoria ternatea Linn;.” 2014. Thesis, Mahatma Gandhi University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/25741.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jacob, Lijy. “Anticancer studies of Clitoria ternatea Linn;.” 2014. Web. 15 Jan 2021.

Vancouver:

Jacob L. Anticancer studies of Clitoria ternatea Linn;. [Internet] [Thesis]. Mahatma Gandhi University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25741.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jacob L. Anticancer studies of Clitoria ternatea Linn;. [Thesis]. Mahatma Gandhi University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25741

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of KwaZulu-Natal

29. Faya, Mbuso. Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening.

Degree: 2015, University of KwaZulu-Natal

Abstract available in PDF file. Advisors/Committee Members: Karpoormath, Rajshekhar. (advisor).

Subjects/Keywords: Antineoplastic agents.; Biological screening.; Novel quinolone.; Anticancer agents.

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Faya, M. (2015). Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/14922

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Faya, Mbuso. “Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening.” 2015. Thesis, University of KwaZulu-Natal. Accessed January 15, 2021. http://hdl.handle.net/10413/14922.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Faya, Mbuso. “Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening.” 2015. Web. 15 Jan 2021.

Vancouver:

Faya M. Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening. [Internet] [Thesis]. University of KwaZulu-Natal; 2015. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10413/14922.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Faya M. Novel quinolone substituted urea and thiourea derivatives as anti-microbial and anti-cancer agents : design, synthesis and biological screening. [Thesis]. University of KwaZulu-Natal; 2015. Available from: http://hdl.handle.net/10413/14922

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Duquesne University

30. Devambatla, Ravi Kumar Vyas. Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase.

Degree: PhD, Medicinal Chemistry, 2015, Duquesne University

 This dissertation describes an introduction, background and research progress in the areas of multitargeted single agents and tubulin inhibitors in cancer chemotherapy and selective Toxoplasma… (more)

Subjects/Keywords: Anticancer Agents; Antiopportunistic Agents; Furo[2; 3-d]pyrimidines; Pyrimido[4; 5-b]indoles; Tubulin Inhibitors

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Devambatla, R. K. V. (2015). Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/482

Chicago Manual of Style (16th Edition):

Devambatla, Ravi Kumar Vyas. “Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase.” 2015. Doctoral Dissertation, Duquesne University. Accessed January 15, 2021. https://dsc.duq.edu/etd/482.

MLA Handbook (7th Edition):

Devambatla, Ravi Kumar Vyas. “Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase.” 2015. Web. 15 Jan 2021.

Vancouver:

Devambatla RKV. Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Jan 15]. Available from: https://dsc.duq.edu/etd/482.

Council of Science Editors:

Devambatla RKV. Design and synthesis of pyrimido[4,5-b]indoles and furo[2,3-d]pyrimidines as single agents with combination chemotherapy potential or as inhibitors of tubulin or thymidylate synthase. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/482

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