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You searched for subject:(Structure activity Relationship). Showing records 1 – 30 of 172 total matches.

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Northeastern University

1. Sharif, Ehesan U. Synthetic study toward angucycline and resin glycoside natural products.

Degree: PhD, Department of Chemistry and Chemical Biology, 2013, Northeastern University

 Angucycline natural products containing carbohydrate motifs have long been known for their impressive biological activities. Apart from their interesting bioactivities, these complex natural products are… (more)

Subjects/Keywords: angucycline; resin glycoside; natural products; Structure Activity Relationship; Chemistry

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APA (6th Edition):

Sharif, E. U. (2013). Synthetic study toward angucycline and resin glycoside natural products. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003218

Chicago Manual of Style (16th Edition):

Sharif, Ehesan U. “Synthetic study toward angucycline and resin glycoside natural products.” 2013. Doctoral Dissertation, Northeastern University. Accessed June 25, 2019. http://hdl.handle.net/2047/d20003218.

MLA Handbook (7th Edition):

Sharif, Ehesan U. “Synthetic study toward angucycline and resin glycoside natural products.” 2013. Web. 25 Jun 2019.

Vancouver:

Sharif EU. Synthetic study toward angucycline and resin glycoside natural products. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2047/d20003218.

Council of Science Editors:

Sharif EU. Synthetic study toward angucycline and resin glycoside natural products. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003218


University of Louisville

2. Wu, Huihui, 1979-. Structure-activity relationship model for estrogen receptor ligands.

Degree: MS, 2012, University of Louisville

 Xenoestrogens are spread throughout the environment affecting our daily lives and may produce potential toxic effects on human health. The purpose of this study was… (more)

Subjects/Keywords: Structure-activity relationship; Cat-SAR; Endocrine disruptor; Estrogen

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APA (6th Edition):

Wu, Huihui, 1. (2012). Structure-activity relationship model for estrogen receptor ligands. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/1596 ; https://ir.library.louisville.edu/etd/1596

Chicago Manual of Style (16th Edition):

Wu, Huihui, 1979-. “Structure-activity relationship model for estrogen receptor ligands.” 2012. Masters Thesis, University of Louisville. Accessed June 25, 2019. 10.18297/etd/1596 ; https://ir.library.louisville.edu/etd/1596.

MLA Handbook (7th Edition):

Wu, Huihui, 1979-. “Structure-activity relationship model for estrogen receptor ligands.” 2012. Web. 25 Jun 2019.

Vancouver:

Wu, Huihui 1. Structure-activity relationship model for estrogen receptor ligands. [Internet] [Masters thesis]. University of Louisville; 2012. [cited 2019 Jun 25]. Available from: 10.18297/etd/1596 ; https://ir.library.louisville.edu/etd/1596.

Council of Science Editors:

Wu, Huihui 1. Structure-activity relationship model for estrogen receptor ligands. [Masters Thesis]. University of Louisville; 2012. Available from: 10.18297/etd/1596 ; https://ir.library.louisville.edu/etd/1596


University of California – Santa Cruz

3. Effenberger, Kerstin. Dissecting spliceosome function with small-molecule inhibitors.

Degree: Molecular Cell and Developmental Biology, 2015, University of California – Santa Cruz

 In eukaryotes, a crucial step in gene expression is pre-mRNA splicing by the spliceosome. The spliceosome is a macromolecular machine that removes intervening intron sequences… (more)

Subjects/Keywords: Molecular biology; Biochemistry; high-throughput; inhibitor; SF3B1; spliceosome; structure-activity relationship

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APA (6th Edition):

Effenberger, K. (2015). Dissecting spliceosome function with small-molecule inhibitors. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/4ht1998w

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):

Effenberger, Kerstin. “Dissecting spliceosome function with small-molecule inhibitors.” 2015. Thesis, University of California – Santa Cruz. Accessed June 25, 2019. http://www.escholarship.org/uc/item/4ht1998w.

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

MLA Handbook (7th Edition):

Effenberger, Kerstin. “Dissecting spliceosome function with small-molecule inhibitors.” 2015. Web. 25 Jun 2019.

Vancouver:

Effenberger K. Dissecting spliceosome function with small-molecule inhibitors. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/4ht1998w.

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

Council of Science Editors:

Effenberger K. Dissecting spliceosome function with small-molecule inhibitors. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/4ht1998w

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


University of Sydney

4. Jorgensen, William. The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands .

Degree: 2016, University of Sydney

 This thesis describes the design, synthesis and pharmacological profile of a library of selective oxytocin receptor ligands. Oxytocin and arginine vasopressin are structurally related neuropeptides… (more)

Subjects/Keywords: Structure - Activity - Relationship; Non-Peptidic; Oxytocin Receptor; Agonist

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APA (6th Edition):

Jorgensen, W. (2016). The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16542

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):

Jorgensen, William. “The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands .” 2016. Thesis, University of Sydney. Accessed June 25, 2019. http://hdl.handle.net/2123/16542.

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

MLA Handbook (7th Edition):

Jorgensen, William. “The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands .” 2016. Web. 25 Jun 2019.

Vancouver:

Jorgensen W. The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands . [Internet] [Thesis]. University of Sydney; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2123/16542.

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

Council of Science Editors:

Jorgensen W. The Discovery of Selective Non-Peptidic Oxytocin Receptor Ligands . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/16542

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


Montana Tech

5. Swain III, Paul Whitney. Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library.

Degree: PhD, 2010, Montana Tech

  Infectious diseases will always be a public health concern. The incidence of bacterial strains found in clinical settings that exhibit resistance to our current… (more)

Subjects/Keywords: antibiotic; compound library; drug; natural product; nonactin; structure activity relationship

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APA (6th Edition):

Swain III, P. W. (2010). Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/939

Chicago Manual of Style (16th Edition):

Swain III, Paul Whitney. “Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library.” 2010. Doctoral Dissertation, Montana Tech. Accessed June 25, 2019. https://scholarworks.umt.edu/etd/939.

MLA Handbook (7th Edition):

Swain III, Paul Whitney. “Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library.” 2010. Web. 25 Jun 2019.

Vancouver:

Swain III PW. Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library. [Internet] [Doctoral dissertation]. Montana Tech; 2010. [cited 2019 Jun 25]. Available from: https://scholarworks.umt.edu/etd/939.

Council of Science Editors:

Swain III PW. Synthesis and Structure Activity Relationship Studies of a Natural Product-Derived Compound Library. [Doctoral Dissertation]. Montana Tech; 2010. Available from: https://scholarworks.umt.edu/etd/939


Virginia Tech

6. Congdon, Molly D. Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors.

Degree: PhD, Chemistry, 2016, Virginia Tech

 A variety of diseases including Alzheimer's disease, asthma, cancer, fibrosis, multiple sclerosis, and sickle cell disease have been associated with elevated levels of sphingosine-1-phosphate (S1P).… (more)

Subjects/Keywords: sphingosine; sphingosine kinase; sphingosine-1-phosphate; structure-activity relationship; molecular docking

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APA (6th Edition):

Congdon, M. D. (2016). Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/82129

Chicago Manual of Style (16th Edition):

Congdon, Molly D. “Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors.” 2016. Doctoral Dissertation, Virginia Tech. Accessed June 25, 2019. http://hdl.handle.net/10919/82129.

MLA Handbook (7th Edition):

Congdon, Molly D. “Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors.” 2016. Web. 25 Jun 2019.

Vancouver:

Congdon MD. Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10919/82129.

Council of Science Editors:

Congdon MD. Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/82129


University of South Florida

7. Van Horn, Kurt Steven. Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines.

Degree: 2013, University of South Florida

 Thirty-three 1,4-dihydropyridine diastereomeric pairs were synthesized and the structure-activity relationship studied in a Plasmodium falciparum in vitro model. Twenty-nine of these derivatives contained a 6-position… (more)

Subjects/Keywords: Acinetobacter baumannii; antimicrobial; leishmaniasis; malaria; Staphylococcus aureus; Structure-Activity Relationship; Chemistry

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APA (6th Edition):

Van Horn, K. S. (2013). Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4784

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):

Van Horn, Kurt Steven. “Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines.” 2013. Thesis, University of South Florida. Accessed June 25, 2019. https://scholarcommons.usf.edu/etd/4784.

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

MLA Handbook (7th Edition):

Van Horn, Kurt Steven. “Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines.” 2013. Web. 25 Jun 2019.

Vancouver:

Van Horn KS. Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines. [Internet] [Thesis]. University of South Florida; 2013. [cited 2019 Jun 25]. Available from: https://scholarcommons.usf.edu/etd/4784.

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

Council of Science Editors:

Van Horn KS. Anti-parasitic and anti-bacterial agents: Studies on 1,4-dihydropyridines and 2,4-diaminoquinazolines. [Thesis]. University of South Florida; 2013. Available from: https://scholarcommons.usf.edu/etd/4784

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


University of South Florida

8. Giulianotti, Marcello. The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation.

Degree: 2016, University of South Florida

 The goal of this work is to demonstrate the utility of using systematically formatted mixture based libraries as part of the drug discovery processes. While… (more)

Subjects/Keywords: Positional Scanning Libraries; Scaffold Ranking; Structure Activity Relationship; Tool Compounds; Chemistry

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APA (6th Edition):

Giulianotti, M. (2016). The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/6088

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):

Giulianotti, Marcello. “The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation.” 2016. Thesis, University of South Florida. Accessed June 25, 2019. https://scholarcommons.usf.edu/etd/6088.

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

MLA Handbook (7th Edition):

Giulianotti, Marcello. “The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation.” 2016. Web. 25 Jun 2019.

Vancouver:

Giulianotti M. The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation. [Internet] [Thesis]. University of South Florida; 2016. [cited 2019 Jun 25]. Available from: https://scholarcommons.usf.edu/etd/6088.

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

Council of Science Editors:

Giulianotti M. The Use of Synthetic Mixture Based Libraries to Identify Hit Compounds for ESKAPE Pathogens, Leishmaniasis, and Inhibitors of Palmitoylation. [Thesis]. University of South Florida; 2016. Available from: https://scholarcommons.usf.edu/etd/6088

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


University of South Florida

9. Barber, Megan Marie. 2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity.

Degree: 2015, University of South Florida

 Herein 47 2,4-disubstituted quinazolines were synthesized and tested against Leishmania donovani intracellular amastigotes. A structure-activity relationship was conducted and lead to the identification of quinazolines… (more)

Subjects/Keywords: Leishmaniasis; Acinetobacter baumannii; antimicrobial; structure-activity relationship; Chemistry

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APA (6th Edition):

Barber, M. M. (2015). 2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5840

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):

Barber, Megan Marie. “2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity.” 2015. Thesis, University of South Florida. Accessed June 25, 2019. https://scholarcommons.usf.edu/etd/5840.

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

MLA Handbook (7th Edition):

Barber, Megan Marie. “2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity.” 2015. Web. 25 Jun 2019.

Vancouver:

Barber MM. 2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity. [Internet] [Thesis]. University of South Florida; 2015. [cited 2019 Jun 25]. Available from: https://scholarcommons.usf.edu/etd/5840.

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

Council of Science Editors:

Barber MM. 2,4-Disubstituted Quinazolines with Antileishmanial or Antibacterial Activity. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5840

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


Australian National University

10. Bernardo, Paul Huntington. Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds .

Degree: 2011, Australian National University

 Calothrixin A and B are novel pentacycIic qui nones that have been isolated from the Calothrix cyanobacteria. The calothrixins exhibit anti proliferative activity against chloroquine… (more)

Subjects/Keywords: quinone; calothrixin; Structure-Activity Relationship Studies; QSAR; medicinal chemistry; QSAR

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APA (6th Edition):

Bernardo, P. H. (2011). Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/7171

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):

Bernardo, Paul Huntington. “Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds .” 2011. Thesis, Australian National University. Accessed June 25, 2019. http://hdl.handle.net/1885/7171.

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

MLA Handbook (7th Edition):

Bernardo, Paul Huntington. “Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds .” 2011. Web. 25 Jun 2019.

Vancouver:

Bernardo PH. Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds . [Internet] [Thesis]. Australian National University; 2011. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1885/7171.

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

Council of Science Editors:

Bernardo PH. Synthesis and structure-activity relationship studies of the calothrixins and other redox-active compounds . [Thesis]. Australian National University; 2011. Available from: http://hdl.handle.net/1885/7171

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


University of New South Wales

11. Zhang, Yuqi. Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents.

Degree: Chemistry, 2018, University of New South Wales

 This thesis describes the exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents via synthesizing natural product Marthiapeptide A and series of trithiazole containing… (more)

Subjects/Keywords: Total synthesis; Thiazole; Natural product; Anti-cancer; Fragments; Structure activity relationship

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APA (6th Edition):

Zhang, Y. (2018). Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/61446 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:55644/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Zhang, Yuqi. “Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents.” 2018. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/61446 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:55644/SOURCE02?view=true.

MLA Handbook (7th Edition):

Zhang, Yuqi. “Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents.” 2018. Web. 25 Jun 2019.

Vancouver:

Zhang Y. Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/61446 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:55644/SOURCE02?view=true.

Council of Science Editors:

Zhang Y. Exploration of novel 2,4-linked thiazole containing molecules as anti-cancer agents. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/61446 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:55644/SOURCE02?view=true


University of New South Wales

12. Wahyudi, Hendra. Development of lead structures that are cytotoxic and are derived from macrocycle natural products.

Degree: Chemistry, 2014, University of New South Wales

 This thesis describes the development of lead structures from two macrocyclic peptide-based natural products: Sansalvamide A (San A) and Sanguinamide B (San B). San A,… (more)

Subjects/Keywords: Natural Product; Macrocycle; Structure-Activity Relationship; Cytotoxic; Macrocyclic Peptide

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APA (6th Edition):

Wahyudi, H. (2014). Development of lead structures that are cytotoxic and are derived from macrocycle natural products. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Wahyudi, Hendra. “Development of lead structures that are cytotoxic and are derived from macrocycle natural products.” 2014. Doctoral Dissertation, University of New South Wales. Accessed June 25, 2019. http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true.

MLA Handbook (7th Edition):

Wahyudi, Hendra. “Development of lead structures that are cytotoxic and are derived from macrocycle natural products.” 2014. Web. 25 Jun 2019.

Vancouver:

Wahyudi H. Development of lead structures that are cytotoxic and are derived from macrocycle natural products. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Jun 25]. Available from: http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true.

Council of Science Editors:

Wahyudi H. Development of lead structures that are cytotoxic and are derived from macrocycle natural products. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true


Uniwersytet im. Adama Mickiewicza w Poznaniu

13. Antoszczak, Michał. Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny .

Degree: 2016, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Badania naukowe z ostatnich kilku lat udowodniły, że salinomycyna hamuje namnażanie ludzkich komórek nowotworowych oraz doprowadza do ich śmierci. W literaturze brakowało natomiast doniesień poświęconych… (more)

Subjects/Keywords: antybiotyki jonoforowe; ionophore antibiotics; salinomycyna; salinomycin; aktywność przeciwnowotworowa; anticancer activity; aktywność przeciwdrobnoustrojowa; antimicrobial activity; korelacja struktura-bioaktywność; structure-activity relationship

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APA (6th Edition):

Antoszczak, M. (2016). Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/14670

Chicago Manual of Style (16th Edition):

Antoszczak, Michał. “Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny .” 2016. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed June 25, 2019. http://hdl.handle.net/10593/14670.

MLA Handbook (7th Edition):

Antoszczak, Michał. “Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny .” 2016. Web. 25 Jun 2019.

Vancouver:

Antoszczak M. Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10593/14670.

Council of Science Editors:

Antoszczak M. Synteza, badania strukturalne i spektroskopowe oraz aktywność przeciwnowotworowa i przeciwdrobnoustrojowa nowych pochodnych salinomycyny . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2016. Available from: http://hdl.handle.net/10593/14670

14. Pâmela Padaratz. Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas.

Degree: 2009, Universidade do Vale do Itajaí

Chalcones are chemically designated as α, β - unsaturated ketones with two aromatic rings, one connected directly to a ketone function (ring A), and the… (more)

Subjects/Keywords: benzofuranonas; chalconas; relação estrutura-atividade; síntese; FARMACIA; benzofuranones; chalcones; structure-activity relationship; synthesis

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APA (6th Edition):

Padaratz, P. (2009). Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas. (Thesis). Universidade do Vale do Itajaí. Retrieved from http://www6.univali.br/tede/tde_busca/arquivo.php?codArquivo=704

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):

Padaratz, Pâmela. “Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas.” 2009. Thesis, Universidade do Vale do Itajaí. Accessed June 25, 2019. http://www6.univali.br/tede/tde_busca/arquivo.php?codArquivo=704.

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

MLA Handbook (7th Edition):

Padaratz, Pâmela. “Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas.” 2009. Web. 25 Jun 2019.

Vancouver:

Padaratz P. Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas. [Internet] [Thesis]. Universidade do Vale do Itajaí; 2009. [cited 2019 Jun 25]. Available from: http://www6.univali.br/tede/tde_busca/arquivo.php?codArquivo=704.

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

Council of Science Editors:

Padaratz P. Síntese e avaliação do potencial biológico de chalconas e substâncias relacionadas. [Thesis]. Universidade do Vale do Itajaí; 2009. Available from: http://www6.univali.br/tede/tde_busca/arquivo.php?codArquivo=704

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


University of Vermont

15. Harvey, Rebecca. The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol.

Degree: PhD, Chemistry, 2016, University of Vermont

  Aerosols play important roles in atmospheric and environmental processes. Not only do they impact human health, they also affect visibility and climate. Despite recent… (more)

Subjects/Keywords: atmospheric aerosol; green leaf volatile; ozonolysis; secondary organic aerosol; structure activity relationship; Atmospheric Sciences; Chemistry

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

APA (6th Edition):

Harvey, R. (2016). The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/556

Chicago Manual of Style (16th Edition):

Harvey, Rebecca. “The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol.” 2016. Doctoral Dissertation, University of Vermont. Accessed June 25, 2019. https://scholarworks.uvm.edu/graddis/556.

MLA Handbook (7th Edition):

Harvey, Rebecca. “The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol.” 2016. Web. 25 Jun 2019.

Vancouver:

Harvey R. The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol. [Internet] [Doctoral dissertation]. University of Vermont; 2016. [cited 2019 Jun 25]. Available from: https://scholarworks.uvm.edu/graddis/556.

Council of Science Editors:

Harvey R. The Role of Green Leafy Plants in Atmospheric Chemistry: Volatile Emissions and Secondary Organic Aerosol. [Doctoral Dissertation]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/graddis/556

16. Nargotra, Amit. Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach.

Degree: Bioinformatics, 2010, Jamia Hamdard University

newline

References p. 177-202

Advisors/Committee Members: Hirwani, R R.

Subjects/Keywords: Drugs-Design; Drugs-Structure-activity relationship

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APA (6th Edition):

Nargotra, A. (2010). Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach. (Thesis). Jamia Hamdard University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/14581

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):

Nargotra, Amit. “Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach.” 2010. Thesis, Jamia Hamdard University. Accessed June 25, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/14581.

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

MLA Handbook (7th Edition):

Nargotra, Amit. “Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach.” 2010. Web. 25 Jun 2019.

Vancouver:

Nargotra A. Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach. [Internet] [Thesis]. Jamia Hamdard University; 2010. [cited 2019 Jun 25]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14581.

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

Council of Science Editors:

Nargotra A. Structure prediction and molecular modeling analysis of therapeutically important targets using in silico approach. [Thesis]. Jamia Hamdard University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14581

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

17. Klimenko, Kyrylo. Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre.

Degree: Docteur es, Chimie, 2017, Strasbourg; Institut A.V. Bogatsky de Chimie Physique (Odessa, Ukraine)

De nouveaux antiviraux à large spectre, agissant comme intercalant d'acides nucléiques, ont été identifiés par criblage virtuel et grâce à des cartes de l’espace chimique.… (more)

Subjects/Keywords: Antiviraux; Espace chimique; Criblage virtuel; Structure-activity relationship; Antiviral; Chemical space; Virtual screening; 615.19

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APA (6th Edition):

Klimenko, K. (2017). Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre. (Doctoral Dissertation). Strasbourg; Institut A.V. Bogatsky de Chimie Physique (Odessa, Ukraine). Retrieved from http://www.theses.fr/2017STRAF008

Chicago Manual of Style (16th Edition):

Klimenko, Kyrylo. “Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre.” 2017. Doctoral Dissertation, Strasbourg; Institut A.V. Bogatsky de Chimie Physique (Odessa, Ukraine). Accessed June 25, 2019. http://www.theses.fr/2017STRAF008.

MLA Handbook (7th Edition):

Klimenko, Kyrylo. “Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre.” 2017. Web. 25 Jun 2019.

Vancouver:

Klimenko K. Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre. [Internet] [Doctoral dissertation]. Strasbourg; Institut A.V. Bogatsky de Chimie Physique (Odessa, Ukraine); 2017. [cited 2019 Jun 25]. Available from: http://www.theses.fr/2017STRAF008.

Council of Science Editors:

Klimenko K. Computer-aided drug design of broad-spectrum antiviral compounds : Conception assistée par ordinateur de composés antiviraux à large spectre. [Doctoral Dissertation]. Strasbourg; Institut A.V. Bogatsky de Chimie Physique (Odessa, Ukraine); 2017. Available from: http://www.theses.fr/2017STRAF008


UCLA

18. Gipson, Raymond Marshall. I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization.

Degree: Chemistry, 2015, UCLA

 Small molecule dCK inhibitors, in combination with pharmacological perturbations of de novo dNTP biosynthetic pathways, can eliminate acute lymphoblastic leukemia cells in animal models. Our… (more)

Subjects/Keywords: Chemistry; Pharmacology; Biodegradable polymers; Deoxycytidine Kinase; Enzyme Inhibitor; Ferrocene; Structure activity relationship

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APA (6th Edition):

Gipson, R. M. (2015). I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8f2586bd

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):

Gipson, Raymond Marshall. “I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization.” 2015. Thesis, UCLA. Accessed June 25, 2019. http://www.escholarship.org/uc/item/8f2586bd.

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

MLA Handbook (7th Edition):

Gipson, Raymond Marshall. “I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization.” 2015. Web. 25 Jun 2019.

Vancouver:

Gipson RM. I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/8f2586bd.

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

Council of Science Editors:

Gipson RM. I) The Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability, II) The Synthesis of Ferrocene-Containing Monomers and Biodegradable Polymers Using Azide-Alkyne Click Chemistry and Ring Opening Polymerization. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/8f2586bd

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


McMaster University

19. Huang, Cheng. PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES.

Degree: MSc, 2016, McMaster University

Anthracycline-based chemotherapy is the mainstay neoadjuvant therapy for breast cancer. However, it is efficacious in only 60% of patients while carrying substantial toxicity. The application… (more)

Subjects/Keywords: breast cancer; p53 mutation; chemotherapy response; phenotypic screening; cytological profiling; structure–activity relationship

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APA (6th Edition):

Huang, C. (2016). PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/18709

Chicago Manual of Style (16th Edition):

Huang, Cheng. “PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES.” 2016. Masters Thesis, McMaster University. Accessed June 25, 2019. http://hdl.handle.net/11375/18709.

MLA Handbook (7th Edition):

Huang, Cheng. “PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES.” 2016. Web. 25 Jun 2019.

Vancouver:

Huang C. PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/11375/18709.

Council of Science Editors:

Huang C. PHENOTYPIC AND CHEMOTHERAPY RESPONSE PROFILING OF P53 WILD-TYPE AND MUTANT HUMAN BREAST CANCER CELL LINES. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/18709


Virginia Tech

20. Childress, Elizabeth Saunders. Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers.

Degree: PhD, Chemistry, 2017, Virginia Tech

 Sphingosine 1-phosphate (S1P) is a cellular signaling molecule that has been implicated in a variety of diseases including cancer, fibrosis, Alzheimer's, and sickle cell disease.… (more)

Subjects/Keywords: Structure-Activity Relationship; Sphingosine Kinase; Sphingosine 1-Phosphate; Mitochondrial Uncoupler; Protonophore; Oxygen Consumption Rate

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APA (6th Edition):

Childress, E. S. (2017). Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/86662

Chicago Manual of Style (16th Edition):

Childress, Elizabeth Saunders. “Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers.” 2017. Doctoral Dissertation, Virginia Tech. Accessed June 25, 2019. http://hdl.handle.net/10919/86662.

MLA Handbook (7th Edition):

Childress, Elizabeth Saunders. “Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers.” 2017. Web. 25 Jun 2019.

Vancouver:

Childress ES. Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10919/86662.

Council of Science Editors:

Childress ES. Structure-Activity Relationship Studies of Sphingosine Kinase Inhibitors and Mitochondrial Uncouplers. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/86662


Uniwersytet im. Adama Mickiewicza w Poznaniu

21. Grześkiewicz, Anita. Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej .

Degree: 2015, Uniwersytet im. Adama Mickiewicza w Poznaniu

 W ramach prowadzonych badań otrzymano nowe kompleksy trifenylocyny z tioamidami, które scharakteryzowano różnymi metodami analitycznymi. Rozwiązano i udokładniono struktury 15 nowych kompleksów o udowodnionej aktywności… (more)

Subjects/Keywords: Relacja struktura-aktywność; structure activity relationship; rozkład gęstości elektronowej; charge density distribution; gęstość elektronowa

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APA (6th Edition):

Grześkiewicz, A. (2015). Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/14017

Chicago Manual of Style (16th Edition):

Grześkiewicz, Anita. “Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej .” 2015. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed June 25, 2019. http://hdl.handle.net/10593/14017.

MLA Handbook (7th Edition):

Grześkiewicz, Anita. “Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej .” 2015. Web. 25 Jun 2019.

Vancouver:

Grześkiewicz A. Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10593/14017.

Council of Science Editors:

Grześkiewicz A. Relacja między strukturą a aktywnością biologiczną kompleksów wybranych metali z tioamidami, potencjalnych leków terapii antynowotworowej . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2015. Available from: http://hdl.handle.net/10593/14017


University of Colorado

22. Nordeen, Patrick. Design and Synthesis of Potential TLR7 and TLR8 Inhibitors.

Degree: MS, 2018, University of Colorado

  Toll-like receptors (TLRs) detect invading viral and bacterial pathogens and play a critical role in the initiation and regulation of the innate immune system.… (more)

Subjects/Keywords: toll-like receptors; inhibitors; structure-activity relationship; ligands; synthesis; Biochemistry; Organic Chemistry

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APA (6th Edition):

Nordeen, P. (2018). Design and Synthesis of Potential TLR7 and TLR8 Inhibitors. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/245

Chicago Manual of Style (16th Edition):

Nordeen, Patrick. “Design and Synthesis of Potential TLR7 and TLR8 Inhibitors.” 2018. Masters Thesis, University of Colorado. Accessed June 25, 2019. https://scholar.colorado.edu/chem_gradetds/245.

MLA Handbook (7th Edition):

Nordeen, Patrick. “Design and Synthesis of Potential TLR7 and TLR8 Inhibitors.” 2018. Web. 25 Jun 2019.

Vancouver:

Nordeen P. Design and Synthesis of Potential TLR7 and TLR8 Inhibitors. [Internet] [Masters thesis]. University of Colorado; 2018. [cited 2019 Jun 25]. Available from: https://scholar.colorado.edu/chem_gradetds/245.

Council of Science Editors:

Nordeen P. Design and Synthesis of Potential TLR7 and TLR8 Inhibitors. [Masters Thesis]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/245


University of California – San Francisco

23. Tran, Hai Long. Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic.

Degree: Chemistry and Chemical Biology, 2017, University of California – San Francisco

 Antibiotics are some of the most important drugs ever developed to save human lives. These drugs are essentially cures for microbial infections. Despite how important… (more)

Subjects/Keywords: Chemistry; Molecular biology; antibiotic; mutagenesis; natural product; structure-activity relationship; thiocillin; thiopeptide

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APA (6th Edition):

Tran, H. L. (2017). Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/45g1j744

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):

Tran, Hai Long. “Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic.” 2017. Thesis, University of California – San Francisco. Accessed June 25, 2019. http://www.escholarship.org/uc/item/45g1j744.

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

MLA Handbook (7th Edition):

Tran, Hai Long. “Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic.” 2017. Web. 25 Jun 2019.

Vancouver:

Tran HL. Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/45g1j744.

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

Council of Science Editors:

Tran HL. Saturation Mutagenesis and Structure-Activity Relationship of a Natural Product Antibiotic. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/45g1j744

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


ETH Zürich

24. Müller, Alex T. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.

Degree: 2018, ETH Zürich

 Bacterial resistance, eradicating the efficiency of many antibiotics, is globally increasing and poses a threat to public health. In parallel, an all-time low number of… (more)

Subjects/Keywords: Antibiotic resistance; Machine learning; Recurrent neural networks; Peptide design; Structure-activity relationship; Artificial intelligence

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APA (6th Edition):

Müller, A. T. (2018). De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/267218

Chicago Manual of Style (16th Edition):

Müller, Alex T. “De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.” 2018. Doctoral Dissertation, ETH Zürich. Accessed June 25, 2019. http://hdl.handle.net/20.500.11850/267218.

MLA Handbook (7th Edition):

Müller, Alex T. “De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.” 2018. Web. 25 Jun 2019.

Vancouver:

Müller AT. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. [Internet] [Doctoral dissertation]. ETH Zürich; 2018. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/20.500.11850/267218.

Council of Science Editors:

Müller AT. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. [Doctoral Dissertation]. ETH Zürich; 2018. Available from: http://hdl.handle.net/20.500.11850/267218


University of Michigan

25. Yestrepsky, Bryan Daniel. Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics.

Degree: PhD, Medicinal Chemistry, 2013, University of Michigan

 Resistance to traditional antibiotics arises largely because killing bacteria or halting their reproduction induces a selective pressure on mutants able to survive treatment. Virulence-attenuating antibiotics… (more)

Subjects/Keywords: Antibiotics; Group a Streptococcus; Structure Activity Relationship; Macromolecular Target Identification; Biofilm Inhibition; Chemistry; Science

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APA (6th Edition):

Yestrepsky, B. D. (2013). Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102329

Chicago Manual of Style (16th Edition):

Yestrepsky, Bryan Daniel. “Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics.” 2013. Doctoral Dissertation, University of Michigan. Accessed June 25, 2019. http://hdl.handle.net/2027.42/102329.

MLA Handbook (7th Edition):

Yestrepsky, Bryan Daniel. “Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics.” 2013. Web. 25 Jun 2019.

Vancouver:

Yestrepsky BD. Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2027.42/102329.

Council of Science Editors:

Yestrepsky BD. Development of a Novel Class of Multifunctional Virulence-Attenuating Antibiotics. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102329


University of Arizona

26. Hall, Sara M. Bradykinin Ligands and Receptors Involved in Neuropathic Pain .

Degree: 2015, University of Arizona

 Neuropathic pain is a prevalent disease with no effective, safe treatments and limited knowledge on the mechanisms involved. One target for neuropathic pain treatment may… (more)

Subjects/Keywords: neuropathic pain; non-opioid Dynorphin A; structure activity relationship; Biochemistry; bradykinin receptors

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APA (6th Edition):

Hall, S. M. (2015). Bradykinin Ligands and Receptors Involved in Neuropathic Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/578606

Chicago Manual of Style (16th Edition):

Hall, Sara M. “Bradykinin Ligands and Receptors Involved in Neuropathic Pain .” 2015. Doctoral Dissertation, University of Arizona. Accessed June 25, 2019. http://hdl.handle.net/10150/578606.

MLA Handbook (7th Edition):

Hall, Sara M. “Bradykinin Ligands and Receptors Involved in Neuropathic Pain .” 2015. Web. 25 Jun 2019.

Vancouver:

Hall SM. Bradykinin Ligands and Receptors Involved in Neuropathic Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10150/578606.

Council of Science Editors:

Hall SM. Bradykinin Ligands and Receptors Involved in Neuropathic Pain . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/578606


University of Ottawa

27. Fluet-Chouinard, Adrien. Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy .

Degree: 2019, University of Ottawa

 Prior work in the Durst group had generated more than forty analogs of the potent anticonvulsant isoxylitone isolated isolated from a medicinal plant Delphinium denudatum… (more)

Subjects/Keywords: Synthesis of Analogs; Potential Drug; Treatment of Epilepsy; Anti-epileptic drug; Structure-activity relationship

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

APA (6th Edition):

Fluet-Chouinard, A. (2019). Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39257

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):

Fluet-Chouinard, Adrien. “Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy .” 2019. Thesis, University of Ottawa. Accessed June 25, 2019. http://hdl.handle.net/10393/39257.

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

MLA Handbook (7th Edition):

Fluet-Chouinard, Adrien. “Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy .” 2019. Web. 25 Jun 2019.

Vancouver:

Fluet-Chouinard A. Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10393/39257.

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

Council of Science Editors:

Fluet-Chouinard A. Synthesis of Analogs of a Potential Drug for Treatment of Epilepsy . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39257

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


Kaunas University of Medicine

28. Gaivelytė, Kristina. 5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas.

Degree: Master, Pharmacy, 2010, Kaunas University of Medicine

5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetinių savybių ir struktūros aktyvumo ryšio įvertinimas. K. Gaivelytės magistro baigiamasis darbas. Moksliniai vadovai: dr. V. Petrikaitė, dr. J.… (more)

Subjects/Keywords: Nitrofuraldehido dariniai; Antimikrobinis aktyvumas; Struktūros aktyvumo ryšiai; Toksiškumas; Farmakokinetika; Nitrofuraldehyde derivatives; Antimicrobial activity; Structure – activity relationship; Toxicity; Pharmacokinetics

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APA (6th Edition):

Gaivelytė, Kristina. (2010). 5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas. (Masters Thesis). Kaunas University of Medicine. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_093138-22354 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Gaivelytė, Kristina. “5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas.” 2010. Masters Thesis, Kaunas University of Medicine. Accessed June 25, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_093138-22354 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Gaivelytė, Kristina. “5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas.” 2010. Web. 25 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Gaivelytė, Kristina. 5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas. [Internet] [Masters thesis]. Kaunas University of Medicine; 2010. [cited 2019 Jun 25]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_093138-22354 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Gaivelytė, Kristina. 5-nitrofuraldehido darinių antimikrobinio aktyvumo tyrimas, toksiškumo, farmakokinetikos ir struktūros aktyvumo ryšio įvertinimas. [Masters Thesis]. Kaunas University of Medicine; 2010. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_093138-22354 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

29. Hoffman, Katherine Metcalf. DNA recognition by prokaryotic transcriptional regulators.

Degree: PhD, 2006, Oregon Health Sciences University

Subjects/Keywords: Regulatory Elements, Transcriptional; Molecular Structure; Quantitative Structure-Activity Relationship

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

APA (6th Edition):

Hoffman, K. M. (2006). DNA recognition by prokaryotic transcriptional regulators. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4445JRT ; http://digitalcommons.ohsu.edu/etd/2886

Chicago Manual of Style (16th Edition):

Hoffman, Katherine Metcalf. “DNA recognition by prokaryotic transcriptional regulators.” 2006. Doctoral Dissertation, Oregon Health Sciences University. Accessed June 25, 2019. doi:10.6083/M4445JRT ; http://digitalcommons.ohsu.edu/etd/2886.

MLA Handbook (7th Edition):

Hoffman, Katherine Metcalf. “DNA recognition by prokaryotic transcriptional regulators.” 2006. Web. 25 Jun 2019.

Vancouver:

Hoffman KM. DNA recognition by prokaryotic transcriptional regulators. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2006. [cited 2019 Jun 25]. Available from: doi:10.6083/M4445JRT ; http://digitalcommons.ohsu.edu/etd/2886.

Council of Science Editors:

Hoffman KM. DNA recognition by prokaryotic transcriptional regulators. [Doctoral Dissertation]. Oregon Health Sciences University; 2006. Available from: doi:10.6083/M4445JRT ; http://digitalcommons.ohsu.edu/etd/2886

30. Bocher, Benjamin T.W. Relating Methanogen Community Structure and Function in Anaerobic Digesters.

Degree: 2012, Marquette University

 A deeper understanding of how microbial community structure relates to process function would help improve anaerobic digester design. This dissertation describes both qualitative and quantitative… (more)

Subjects/Keywords: Anaerobic Digestion; Denaturing gradient gel electrophoresis; mcrA gene; microbial community structure; Quantitative Structure Function Relationship; specific methanogenic activity; Environmental Engineering

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

APA (6th Edition):

Bocher, B. T. W. (2012). Relating Methanogen Community Structure and Function in Anaerobic Digesters. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/208

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):

Bocher, Benjamin T W. “Relating Methanogen Community Structure and Function in Anaerobic Digesters.” 2012. Thesis, Marquette University. Accessed June 25, 2019. https://epublications.marquette.edu/dissertations_mu/208.

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

MLA Handbook (7th Edition):

Bocher, Benjamin T W. “Relating Methanogen Community Structure and Function in Anaerobic Digesters.” 2012. Web. 25 Jun 2019.

Vancouver:

Bocher BTW. Relating Methanogen Community Structure and Function in Anaerobic Digesters. [Internet] [Thesis]. Marquette University; 2012. [cited 2019 Jun 25]. Available from: https://epublications.marquette.edu/dissertations_mu/208.

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

Council of Science Editors:

Bocher BTW. Relating Methanogen Community Structure and Function in Anaerobic Digesters. [Thesis]. Marquette University; 2012. Available from: https://epublications.marquette.edu/dissertations_mu/208

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

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