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You searched for subject:(Medicinal Pharmaceutical Chemistry). Showing records 1 – 30 of 345 total matches.

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1. Mishra, Sanket J. Structure-Based Design of Grp94-Selective Inhibitors.

Degree: MS, Medicinal Chemistry, 2014, University of Kansas

 Heat shock protein 90 KDa (Hsp90) belongs to family of proteins called molecular chaperone that are associated with protein folding and maturation. Hsp90 clients play… (more)

Subjects/Keywords: Pharmaceutical sciences; Chemistry; Medicinal Chemistry

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APA (6th Edition):

Mishra, S. J. (2014). Structure-Based Design of Grp94-Selective Inhibitors. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21649

Chicago Manual of Style (16th Edition):

Mishra, Sanket J. “Structure-Based Design of Grp94-Selective Inhibitors.” 2014. Masters Thesis, University of Kansas. Accessed February 25, 2020. http://hdl.handle.net/1808/21649.

MLA Handbook (7th Edition):

Mishra, Sanket J. “Structure-Based Design of Grp94-Selective Inhibitors.” 2014. Web. 25 Feb 2020.

Vancouver:

Mishra SJ. Structure-Based Design of Grp94-Selective Inhibitors. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/1808/21649.

Council of Science Editors:

Mishra SJ. Structure-Based Design of Grp94-Selective Inhibitors. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21649


Northeastern University

2. Johnston, Meghan Ryan. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 The endocannabinoid system includes signaling ligands for the cannabinoid receptors, (CB1, CB2) as well as the enzymes that that are responsible for their biosynthesis and… (more)

Subjects/Keywords: Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Johnston, M. R. (2012). Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002760

Chicago Manual of Style (16th Edition):

Johnston, Meghan Ryan. “Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.” 2012. Doctoral Dissertation, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20002760.

MLA Handbook (7th Edition):

Johnston, Meghan Ryan. “Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.” 2012. Web. 25 Feb 2020.

Vancouver:

Johnston MR. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20002760.

Council of Science Editors:

Johnston MR. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002760


Virginia Commonwealth University

3. Boice, Ashley. DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS.

Degree: PhD, Pharmaceutical Sciences, 2018, Virginia Commonwealth University

  Neurodegenerative diseases are a class of conditions that lead to progressive atrophy of different parts of the central nervous system (CNS). These diseases lead… (more)

Subjects/Keywords: Medicinal and Pharmaceutical Chemistry

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APA (6th Edition):

Boice, A. (2018). DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5372

Chicago Manual of Style (16th Edition):

Boice, Ashley. “DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS.” 2018. Doctoral Dissertation, Virginia Commonwealth University. Accessed February 25, 2020. https://scholarscompass.vcu.edu/etd/5372.

MLA Handbook (7th Edition):

Boice, Ashley. “DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS.” 2018. Web. 25 Feb 2020.

Vancouver:

Boice A. DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2018. [cited 2020 Feb 25]. Available from: https://scholarscompass.vcu.edu/etd/5372.

Council of Science Editors:

Boice A. DEVELOPMENT OF SMALL MOLECULE NEUROPROTECTANTS. [Doctoral Dissertation]. Virginia Commonwealth University; 2018. Available from: https://scholarscompass.vcu.edu/etd/5372


University of Washington

4. Chapman, John D. Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response.

Degree: PhD, 2013, University of Washington

 Mass spectrometry is a powerful proteomics tool. Advancements in instrumentation and data acquisition techniques allow researchers to identify and quantify thousands of proteins from cellular… (more)

Subjects/Keywords: Pharmaceutical sciences; medicinal chemistry

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APA (6th Edition):

Chapman, J. D. (2013). Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/24143

Chicago Manual of Style (16th Edition):

Chapman, John D. “Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response.” 2013. Doctoral Dissertation, University of Washington. Accessed February 25, 2020. http://hdl.handle.net/1773/24143.

MLA Handbook (7th Edition):

Chapman, John D. “Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response.” 2013. Web. 25 Feb 2020.

Vancouver:

Chapman JD. Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/1773/24143.

Council of Science Editors:

Chapman JD. Data-independent mass spectrometry strategies for the identification of atRA-mediated protein signatures of differential cellular response. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/24143


Virginia Commonwealth University

5. Raborg, Thomas. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.

Degree: MS, Pharmaceutical Sciences, 2014, Virginia Commonwealth University

  Chemokine receptor CCR5 (CCR5) is a G-protein coupled receptor (GPCR) predominantly expressed on leukocytes, or white blood cells.1–3 During inflammation, the body releases chemokines… (more)

Subjects/Keywords: Medicinal and Pharmaceutical Chemistry

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APA (6th Edition):

Raborg, T. (2014). Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553

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):

Raborg, Thomas. “Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.” 2014. Thesis, Virginia Commonwealth University. Accessed February 25, 2020. https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553.

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

MLA Handbook (7th Edition):

Raborg, Thomas. “Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.” 2014. Web. 25 Feb 2020.

Vancouver:

Raborg T. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. [Internet] [Thesis]. Virginia Commonwealth University; 2014. [cited 2020 Feb 25]. Available from: https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553.

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

Council of Science Editors:

Raborg T. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. [Thesis]. Virginia Commonwealth University; 2014. Available from: https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553

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


McMaster University

6. Edem, Patricia. PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING.

Degree: MSc, 2011, McMaster University

This thesis describes the initial steps towards the use of dipeptidyl acyloxymethyl ketones as a platform to develop molecular imaging (MI) probes for cancer.… (more)

Subjects/Keywords: cathepsin B; acyloxymethyl ketones; Medicinal-Pharmaceutical Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Edem, P. (2011). PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/10513

Chicago Manual of Style (16th Edition):

Edem, Patricia. “PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING.” 2011. Masters Thesis, McMaster University. Accessed February 25, 2020. http://hdl.handle.net/11375/10513.

MLA Handbook (7th Edition):

Edem, Patricia. “PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING.” 2011. Web. 25 Feb 2020.

Vancouver:

Edem P. PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/11375/10513.

Council of Science Editors:

Edem P. PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/10513


University of Nevada – Las Vegas

7. Serrano, Pauline Nancy. Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid.

Degree: MSin Chemistry, Chemistry, 2011, University of Nevada – Las Vegas

  Rhenium was used as an analog for Technetium to study the electrochemical redox properties because the two elements share the same stable oxidation states… (more)

Subjects/Keywords: Chemistry; Medicinal-Pharmaceutical Chemistry; Physical Chemistry; Radiochemistry

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APA (6th Edition):

Serrano, P. N. (2011). Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid. (Masters Thesis). University of Nevada – Las Vegas. Retrieved from https://digitalscholarship.unlv.edu/thesesdissertations/1234

Chicago Manual of Style (16th Edition):

Serrano, Pauline Nancy. “Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid.” 2011. Masters Thesis, University of Nevada – Las Vegas. Accessed February 25, 2020. https://digitalscholarship.unlv.edu/thesesdissertations/1234.

MLA Handbook (7th Edition):

Serrano, Pauline Nancy. “Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid.” 2011. Web. 25 Feb 2020.

Vancouver:

Serrano PN. Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid. [Internet] [Masters thesis]. University of Nevada – Las Vegas; 2011. [cited 2020 Feb 25]. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/1234.

Council of Science Editors:

Serrano PN. Electrochemistry of technetium analogues rhenium and molybdenum in room temperature ionic liquid. [Masters Thesis]. University of Nevada – Las Vegas; 2011. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/1234


University of Arkansas

8. Roberts, Jesse Leland. Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO.

Degree: MSChE, 2017, University of Arkansas

  Biotherapeutic drugs, derived from biological molecules such as proteins and DNA, are becoming an integral and exceptionally critical aspect of modern medicine. Compared to… (more)

Subjects/Keywords: Biotherapeutic; Green Chemistry; Peptoid; protein; Chemical Engineering; Medicinal and Pharmaceutical Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Roberts, J. L. (2017). Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/2581

Chicago Manual of Style (16th Edition):

Roberts, Jesse Leland. “Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO.” 2017. Masters Thesis, University of Arkansas. Accessed February 25, 2020. https://scholarworks.uark.edu/etd/2581.

MLA Handbook (7th Edition):

Roberts, Jesse Leland. “Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO.” 2017. Web. 25 Feb 2020.

Vancouver:

Roberts JL. Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO. [Internet] [Masters thesis]. University of Arkansas; 2017. [cited 2020 Feb 25]. Available from: https://scholarworks.uark.edu/etd/2581.

Council of Science Editors:

Roberts JL. Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO. [Masters Thesis]. University of Arkansas; 2017. Available from: https://scholarworks.uark.edu/etd/2581


Michigan Technological University

9. Yan, Xin. SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS.

Degree: PhD, Department of Chemistry, 2019, Michigan Technological University

  My thesis is focused on the development of fluorescent probes for biosensing and bioimaging within specific organelles. My main research efforts are mainly focused… (more)

Subjects/Keywords: FLUORESCENT MOLECULAR PROBES; Biochemistry; Medicinal and Pharmaceutical Chemistry; Medicinal-Pharmaceutical Chemistry; Molecular Biology; Organic Chemistry

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APA (6th Edition):

Yan, X. (2019). SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS. (Doctoral Dissertation). Michigan Technological University. Retrieved from https://digitalcommons.mtu.edu/etdr/917

Chicago Manual of Style (16th Edition):

Yan, Xin. “SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS.” 2019. Doctoral Dissertation, Michigan Technological University. Accessed February 25, 2020. https://digitalcommons.mtu.edu/etdr/917.

MLA Handbook (7th Edition):

Yan, Xin. “SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS.” 2019. Web. 25 Feb 2020.

Vancouver:

Yan X. SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS. [Internet] [Doctoral dissertation]. Michigan Technological University; 2019. [cited 2020 Feb 25]. Available from: https://digitalcommons.mtu.edu/etdr/917.

Council of Science Editors:

Yan X. SMALL MOLECULE-BASED FLUORESCENT MOLECULAR PROBES FOR FACILITATING BIOMEDICAL RESEARCH: RATIONAL DESIGN AND BIOIMAGING APPLICATIONS. [Doctoral Dissertation]. Michigan Technological University; 2019. Available from: https://digitalcommons.mtu.edu/etdr/917


University of Montana

10. Gutierrez, Mathew M. XFlow: An algorithm for extracting ion chromatograms.

Degree: MS, 2019, University of Montana

  Abstract: Mass spectrometry is a fundamental tool for modern proteomics. The increasing availability of mass spectrometry data paired with the increasing sensitivity and fidelity… (more)

Subjects/Keywords: mass spectrometry; proteomics; annotation; segmentation; Analytical Chemistry; Medicinal and Pharmaceutical Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Gutierrez, M. M. (2019). XFlow: An algorithm for extracting ion chromatograms. (Masters Thesis). University of Montana. Retrieved from https://scholarworks.umt.edu/etd/11491

Chicago Manual of Style (16th Edition):

Gutierrez, Mathew M. “XFlow: An algorithm for extracting ion chromatograms.” 2019. Masters Thesis, University of Montana. Accessed February 25, 2020. https://scholarworks.umt.edu/etd/11491.

MLA Handbook (7th Edition):

Gutierrez, Mathew M. “XFlow: An algorithm for extracting ion chromatograms.” 2019. Web. 25 Feb 2020.

Vancouver:

Gutierrez MM. XFlow: An algorithm for extracting ion chromatograms. [Internet] [Masters thesis]. University of Montana; 2019. [cited 2020 Feb 25]. Available from: https://scholarworks.umt.edu/etd/11491.

Council of Science Editors:

Gutierrez MM. XFlow: An algorithm for extracting ion chromatograms. [Masters Thesis]. University of Montana; 2019. Available from: https://scholarworks.umt.edu/etd/11491


Temple University

11. Gao, Rong. DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS.

Degree: PhD, 2013, Temple University

Pharmaceutical Sciences

Muscarinic receptors are G-protein-coupled receptors that mediate the response to acetylcholine released from parasympathetic nerves. Although five mAChR subtypes (M1-M5) share a high… (more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Gao, R. (2013). DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,232219

Chicago Manual of Style (16th Edition):

Gao, Rong. “DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS.” 2013. Doctoral Dissertation, Temple University. Accessed February 25, 2020. http://digital.library.temple.edu/u?/p245801coll10,232219.

MLA Handbook (7th Edition):

Gao, Rong. “DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS.” 2013. Web. 25 Feb 2020.

Vancouver:

Gao R. DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2020 Feb 25]. Available from: http://digital.library.temple.edu/u?/p245801coll10,232219.

Council of Science Editors:

Gao R. DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,232219


Temple University

12. Lounsbury, Nicole. Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents.

Degree: PhD, 2016, Temple University

Pharmaceutical Sciences

RNase P is a bacterial ribozyme that catalyzes the maturation of tRNA and is conserved across Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).… (more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Lounsbury, N. (2016). Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,400039

Chicago Manual of Style (16th Edition):

Lounsbury, Nicole. “Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents.” 2016. Doctoral Dissertation, Temple University. Accessed February 25, 2020. http://digital.library.temple.edu/u?/p245801coll10,400039.

MLA Handbook (7th Edition):

Lounsbury, Nicole. “Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents.” 2016. Web. 25 Feb 2020.

Vancouver:

Lounsbury N. Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Feb 25]. Available from: http://digital.library.temple.edu/u?/p245801coll10,400039.

Council of Science Editors:

Lounsbury N. Design, Synthesis and SAR of the First Inhibitors of Methicillin-Resistant S. Aureus RnpA as Novel Antimicrobial Agents. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,400039


University of Central Florida

13. Zhang, Li. Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles.

Degree: 2004, University of Central Florida

 Magnetic materials are currently being developed in the areas of pharmacology and medicinal chemistry for use in applications such as drug delivery and magnetic resonance… (more)

Subjects/Keywords: Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Zhang, L. (2004). Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/6107

Chicago Manual of Style (16th Edition):

Zhang, Li. “Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles.” 2004. Masters Thesis, University of Central Florida. Accessed February 25, 2020. https://stars.library.ucf.edu/etd/6107.

MLA Handbook (7th Edition):

Zhang, Li. “Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles.” 2004. Web. 25 Feb 2020.

Vancouver:

Zhang L. Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles. [Internet] [Masters thesis]. University of Central Florida; 2004. [cited 2020 Feb 25]. Available from: https://stars.library.ucf.edu/etd/6107.

Council of Science Editors:

Zhang L. Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles. [Masters Thesis]. University of Central Florida; 2004. Available from: https://stars.library.ucf.edu/etd/6107


Northeastern University

14. Kallmerten, Amy Elaine. Microwave-accelerated transformations in synthetic organic & medicinal chemistry.

Degree: PhD, Department of Chemistry and Chemical Biology, 2010, Northeastern University

 Microwave assisted organic syntheses have evolved from pioneering work conducted in the 1980's to become a central feature of contemporary organic chemistry. Though initial research… (more)

Subjects/Keywords: organic chemistry; chemistry; microwave; Microwave heating; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Kallmerten, A. E. (2010). Microwave-accelerated transformations in synthetic organic & medicinal chemistry. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20001091

Chicago Manual of Style (16th Edition):

Kallmerten, Amy Elaine. “Microwave-accelerated transformations in synthetic organic & medicinal chemistry.” 2010. Doctoral Dissertation, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20001091.

MLA Handbook (7th Edition):

Kallmerten, Amy Elaine. “Microwave-accelerated transformations in synthetic organic & medicinal chemistry.” 2010. Web. 25 Feb 2020.

Vancouver:

Kallmerten AE. Microwave-accelerated transformations in synthetic organic & medicinal chemistry. [Internet] [Doctoral dissertation]. Northeastern University; 2010. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20001091.

Council of Science Editors:

Kallmerten AE. Microwave-accelerated transformations in synthetic organic & medicinal chemistry. [Doctoral Dissertation]. Northeastern University; 2010. Available from: http://hdl.handle.net/2047/d20001091

15. Perera, K. L. Iresha Sampathi. Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology.

Degree: 2017, Marquette University

 Estrogens (17β-estradiol, E2) have garnered considerable attention in influencing cognitive process in relation to phases of the menstrual cycle, aging and menopausal symptoms. However, hormone… (more)

Subjects/Keywords: Estrogen receptor; Medicinal chemistry; Potency; Selective agonists; Selectivity; Synthesis; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Perera, K. L. I. S. (2017). Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/735

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):

Perera, K L Iresha Sampathi. “Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology.” 2017. Thesis, Marquette University. Accessed February 25, 2020. https://epublications.marquette.edu/dissertations_mu/735.

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

MLA Handbook (7th Edition):

Perera, K L Iresha Sampathi. “Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology.” 2017. Web. 25 Feb 2020.

Vancouver:

Perera KLIS. Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology. [Internet] [Thesis]. Marquette University; 2017. [cited 2020 Feb 25]. Available from: https://epublications.marquette.edu/dissertations_mu/735.

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

Council of Science Editors:

Perera KLIS. Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology. [Thesis]. Marquette University; 2017. Available from: https://epublications.marquette.edu/dissertations_mu/735

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


Northeastern University

16. Kozhushnyan, Anton Igorevich. Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor.

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

 Estradiol tolerates the presence of large functional groups off of the 11-beta position while retaining a reasonable relative binding affinity to Estrogen Receptor-alpha; (ER-alpha). Although… (more)

Subjects/Keywords: estrogen receptor; breast cancer; click chemistry; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Kozhushnyan, A. I. (2013). Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003085

Chicago Manual of Style (16th Edition):

Kozhushnyan, Anton Igorevich. “Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor.” 2013. Masters Thesis, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20003085.

MLA Handbook (7th Edition):

Kozhushnyan, Anton Igorevich. “Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor.” 2013. Web. 25 Feb 2020.

Vancouver:

Kozhushnyan AI. Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20003085.

Council of Science Editors:

Kozhushnyan AI. Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003085


University of Kentucky

17. Miller, Zachary C. THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS.

Degree: 2018, University of Kentucky

 The proteasome is a large protein complex which is responsible for the majority of protein degradation in eukaryotes. Following FDA approval of the first proteasome… (more)

Subjects/Keywords: Proteasome; Screening; Non-Peptide; Cancer; Medicinal Chemistry; Drug Discovery; Medicinal and Pharmaceutical Chemistry; Medicinal Chemistry and Pharmaceutics; Pharmacology

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APA (6th Edition):

Miller, Z. C. (2018). THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/87

Chicago Manual of Style (16th Edition):

Miller, Zachary C. “THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS.” 2018. Doctoral Dissertation, University of Kentucky. Accessed February 25, 2020. https://uknowledge.uky.edu/pharmacy_etds/87.

MLA Handbook (7th Edition):

Miller, Zachary C. “THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS.” 2018. Web. 25 Feb 2020.

Vancouver:

Miller ZC. THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2020 Feb 25]. Available from: https://uknowledge.uky.edu/pharmacy_etds/87.

Council of Science Editors:

Miller ZC. THE DEVELOPMENT OF NOVEL NON-PEPTIDE PROTEASOME INHIBITORS FOR THE TREATMENT OF SOLID TUMORS. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/pharmacy_etds/87


Western Kentucky University

18. Waghwani, Hitesh Kumar. One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains.

Degree: MS, Department of Chemistry, 2015, Western Kentucky University

  On the verge of entering the post-antibiotic era, numerous efforts are in place to regain the losing potential of antibiotics which are proving ineffective… (more)

Subjects/Keywords: Kanamycin; Antibiotic Resistance; Gold Nanoparticles; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Waghwani, H. K. (2015). One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/1455

Chicago Manual of Style (16th Edition):

Waghwani, Hitesh Kumar. “One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains.” 2015. Masters Thesis, Western Kentucky University. Accessed February 25, 2020. https://digitalcommons.wku.edu/theses/1455.

MLA Handbook (7th Edition):

Waghwani, Hitesh Kumar. “One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains.” 2015. Web. 25 Feb 2020.

Vancouver:

Waghwani HK. One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains. [Internet] [Masters thesis]. Western Kentucky University; 2015. [cited 2020 Feb 25]. Available from: https://digitalcommons.wku.edu/theses/1455.

Council of Science Editors:

Waghwani HK. One-Step Synthesis of Kanamycin Functionalized Gold Nanoparticles With Potent Antibacterial Activity Against Resistant Bacterial Strains. [Masters Thesis]. Western Kentucky University; 2015. Available from: https://digitalcommons.wku.edu/theses/1455


Western Michigan University

19. Hinz, Alia V.H. Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein.

Degree: PhD, Chemistry, 2014, Western Michigan University

  Wilson disease protein (WLNP) is a P1b-type ATPase crucial for maintaining copper homeostasis in humans. Mutations in this protein result in the autosomal recessive… (more)

Subjects/Keywords: Wilson disease protein; metal-binding domains; Chemistry; Medicinal and Pharmaceutical Chemistry

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APA (6th Edition):

Hinz, A. V. H. (2014). Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein. (Doctoral Dissertation). Western Michigan University. Retrieved from https://scholarworks.wmich.edu/dissertations/280

Chicago Manual of Style (16th Edition):

Hinz, Alia V H. “Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein.” 2014. Doctoral Dissertation, Western Michigan University. Accessed February 25, 2020. https://scholarworks.wmich.edu/dissertations/280.

MLA Handbook (7th Edition):

Hinz, Alia V H. “Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein.” 2014. Web. 25 Feb 2020.

Vancouver:

Hinz AVH. Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein. [Internet] [Doctoral dissertation]. Western Michigan University; 2014. [cited 2020 Feb 25]. Available from: https://scholarworks.wmich.edu/dissertations/280.

Council of Science Editors:

Hinz AVH. Biophysical Characterization of the First Four Metal-Binding Domains of Human Wilson Disease Protein. [Doctoral Dissertation]. Western Michigan University; 2014. Available from: https://scholarworks.wmich.edu/dissertations/280

20. Holmes, Breanne E. Selective Inhibition Studies of Factor Inhibiting Hif (fih).

Degree: MS(M.S.), Chemistry, 2011, U of Massachusetts : Masters

  The control of oxygen delivery to cells in the body is the result of a small group of primary oxygen sensors, one of the… (more)

Subjects/Keywords: FIH; HIF; Inhibition; Oxygen Sensing; Inorganic Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Holmes, B. E. (2011). Selective Inhibition Studies of Factor Inhibiting Hif (fih). (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/686

Chicago Manual of Style (16th Edition):

Holmes, Breanne E. “Selective Inhibition Studies of Factor Inhibiting Hif (fih).” 2011. Masters Thesis, U of Massachusetts : Masters. Accessed February 25, 2020. http://scholarworks.umass.edu/theses/686.

MLA Handbook (7th Edition):

Holmes, Breanne E. “Selective Inhibition Studies of Factor Inhibiting Hif (fih).” 2011. Web. 25 Feb 2020.

Vancouver:

Holmes BE. Selective Inhibition Studies of Factor Inhibiting Hif (fih). [Internet] [Masters thesis]. U of Massachusetts : Masters; 2011. [cited 2020 Feb 25]. Available from: http://scholarworks.umass.edu/theses/686.

Council of Science Editors:

Holmes BE. Selective Inhibition Studies of Factor Inhibiting Hif (fih). [Masters Thesis]. U of Massachusetts : Masters; 2011. Available from: http://scholarworks.umass.edu/theses/686


East Tennessee State University

21. Van Cleve, Shelley Marie. Synthesis of a Resveratrol Glycinate Derivative.

Degree: MS, Chemistry, 2011, East Tennessee State University

  Recently, the compound resveratrol has had media attention as an anti carcinogen. However, the bioavailability of resveratrol is low in the human system due… (more)

Subjects/Keywords: Polyphenols; Stilbenoid; Resveratrol; Chemistry; Medicinal-Pharmaceutical Chemistry; Physical Sciences and Mathematics

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APA (6th Edition):

Van Cleve, S. M. (2011). Synthesis of a Resveratrol Glycinate Derivative. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/1312

Chicago Manual of Style (16th Edition):

Van Cleve, Shelley Marie. “Synthesis of a Resveratrol Glycinate Derivative.” 2011. Masters Thesis, East Tennessee State University. Accessed February 25, 2020. https://dc.etsu.edu/etd/1312.

MLA Handbook (7th Edition):

Van Cleve, Shelley Marie. “Synthesis of a Resveratrol Glycinate Derivative.” 2011. Web. 25 Feb 2020.

Vancouver:

Van Cleve SM. Synthesis of a Resveratrol Glycinate Derivative. [Internet] [Masters thesis]. East Tennessee State University; 2011. [cited 2020 Feb 25]. Available from: https://dc.etsu.edu/etd/1312.

Council of Science Editors:

Van Cleve SM. Synthesis of a Resveratrol Glycinate Derivative. [Masters Thesis]. East Tennessee State University; 2011. Available from: https://dc.etsu.edu/etd/1312


University of New Orleans

22. Madhav, Monika. Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides.

Degree: PhD, Chemistry, 2013, University of New Orleans

  Invasive fungal infections are a major threat to immune-compromised patients. There is a critical need to develop new antifungal agents because of increasing resistance… (more)

Subjects/Keywords: antifungal; barbiturates; antioxidants; steroids; saccharide; aminoacids; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Madhav, M. (2013). Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1649

Chicago Manual of Style (16th Edition):

Madhav, Monika. “Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides.” 2013. Doctoral Dissertation, University of New Orleans. Accessed February 25, 2020. https://scholarworks.uno.edu/td/1649.

MLA Handbook (7th Edition):

Madhav, Monika. “Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides.” 2013. Web. 25 Feb 2020.

Vancouver:

Madhav M. Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides. [Internet] [Doctoral dissertation]. University of New Orleans; 2013. [cited 2020 Feb 25]. Available from: https://scholarworks.uno.edu/td/1649.

Council of Science Editors:

Madhav M. Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides. [Doctoral Dissertation]. University of New Orleans; 2013. Available from: https://scholarworks.uno.edu/td/1649


University of Kentucky

23. Chakraborty, Ujjwal. OPIOID CODRUGS FOR PAIN MANAGEMENT.

Degree: 2011, University of Kentucky

 Pain is an unpleasant sensory and emotional experience associated with actual or potential tissus damage or described in terms of such damage. Opioids are effective… (more)

Subjects/Keywords: Opioid; Anticonvulsant; Codrug; Antinociception; Pharmacokinetics; Chemistry; Medicinal and Pharmaceutical Chemistry

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APA (6th Edition):

Chakraborty, U. (2011). OPIOID CODRUGS FOR PAIN MANAGEMENT. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/chemistry_etds/2

Chicago Manual of Style (16th Edition):

Chakraborty, Ujjwal. “OPIOID CODRUGS FOR PAIN MANAGEMENT.” 2011. Doctoral Dissertation, University of Kentucky. Accessed February 25, 2020. https://uknowledge.uky.edu/chemistry_etds/2.

MLA Handbook (7th Edition):

Chakraborty, Ujjwal. “OPIOID CODRUGS FOR PAIN MANAGEMENT.” 2011. Web. 25 Feb 2020.

Vancouver:

Chakraborty U. OPIOID CODRUGS FOR PAIN MANAGEMENT. [Internet] [Doctoral dissertation]. University of Kentucky; 2011. [cited 2020 Feb 25]. Available from: https://uknowledge.uky.edu/chemistry_etds/2.

Council of Science Editors:

Chakraborty U. OPIOID CODRUGS FOR PAIN MANAGEMENT. [Doctoral Dissertation]. University of Kentucky; 2011. Available from: https://uknowledge.uky.edu/chemistry_etds/2


Northeastern University

24. Ochiana, Stefan Ovidiu. Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 Neglected tropical diseases (NTDs) represent a group of infectious diseases that blight the lives of approximately one billion people, and collectively cause around 550,000 deaths… (more)

Subjects/Keywords: HAT; NTDs; TbAUK1; TbrPDEB1; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Ochiana, S. O. (2012). Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002770

Chicago Manual of Style (16th Edition):

Ochiana, Stefan Ovidiu. “Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing.” 2012. Doctoral Dissertation, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20002770.

MLA Handbook (7th Edition):

Ochiana, Stefan Ovidiu. “Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing.” 2012. Web. 25 Feb 2020.

Vancouver:

Ochiana SO. Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20002770.

Council of Science Editors:

Ochiana SO. Design, synthesis & evaluation of human Aurora kinase and phosphodiesterase inhibitors for anti-trypanosomal drug discovery via target repurposing. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002770


Northeastern University

25. Alexander, Abigail. Expeditious routes of fluorinations: a comparative study.

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

 This thesis focuses on expeditious and robust modes of fluorination. One such route is microwave-accelerated fluorodenitration and another is a nickel-mediated oxidative addition of fluorine.… (more)

Subjects/Keywords: fluorination; microwave power; Uncaria tomentosa; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Alexander, A. (2013). Expeditious routes of fluorinations: a comparative study. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003111

Chicago Manual of Style (16th Edition):

Alexander, Abigail. “Expeditious routes of fluorinations: a comparative study.” 2013. Masters Thesis, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20003111.

MLA Handbook (7th Edition):

Alexander, Abigail. “Expeditious routes of fluorinations: a comparative study.” 2013. Web. 25 Feb 2020.

Vancouver:

Alexander A. Expeditious routes of fluorinations: a comparative study. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20003111.

Council of Science Editors:

Alexander A. Expeditious routes of fluorinations: a comparative study. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003111


Northeastern University

26. Clements, Zeke. Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease.

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

 Chagas is labeled as a neglected tropical disease (NTD) and has had no successful new drugs in the past 30 years. The current available drugs… (more)

Subjects/Keywords: Chagas Disease; CYP51; Trypanosoma Cruzi; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Clements, Z. (2013). Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20004887

Chicago Manual of Style (16th Edition):

Clements, Zeke. “Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease.” 2013. Masters Thesis, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20004887.

MLA Handbook (7th Edition):

Clements, Zeke. “Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease.” 2013. Web. 25 Feb 2020.

Vancouver:

Clements Z. Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20004887.

Council of Science Editors:

Clements Z. Synthesis of Trypanosoma cruzi lanosterol 14α demethylase (TcCYP51) Inhibitors for the treatment of Chagas disease. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20004887


Northeastern University

27. Yin, Pengcheng. Computational studies of enzyme function and dynamics.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 Understanding of enzyme function and dynamics has an important role in basic biomedical research. Although many experimental and computational methods have been developed in this… (more)

Subjects/Keywords: computational biology; enzyme function; ESR; protein dynamics; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Yin, P. (2012). Computational studies of enzyme function and dynamics. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002789

Chicago Manual of Style (16th Edition):

Yin, Pengcheng. “Computational studies of enzyme function and dynamics.” 2012. Doctoral Dissertation, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20002789.

MLA Handbook (7th Edition):

Yin, Pengcheng. “Computational studies of enzyme function and dynamics.” 2012. Web. 25 Feb 2020.

Vancouver:

Yin P. Computational studies of enzyme function and dynamics. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20002789.

Council of Science Editors:

Yin P. Computational studies of enzyme function and dynamics. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002789


Northeastern University

28. Shelnut, Erin Laine. Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 Prostaglandin ethanolamides (Prostamides) are an emerging class of endogenous eicosanoids derived from cyclooxygenase (COX) metabolism of the endocannabinoid, anandamide. The chemical structure of the prostamides… (more)

Subjects/Keywords: Anandamide; Mosher; Prostaglandin; Prostamide; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Shelnut, E. L. (2012). Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002779

Chicago Manual of Style (16th Edition):

Shelnut, Erin Laine. “Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition.” 2012. Doctoral Dissertation, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20002779.

MLA Handbook (7th Edition):

Shelnut, Erin Laine. “Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition.” 2012. Web. 25 Feb 2020.

Vancouver:

Shelnut EL. Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20002779.

Council of Science Editors:

Shelnut EL. Design & synthesis of prostaglandin ethanolamide covalent probes for the investigation of novel physiological activity and discovery of a prostaglandin intermediate scaffold for FAAH inhibition. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002779


Northeastern University

29. Berger, Victoria Lee. Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry.

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

 N-linked glycosylation is a prevalent post-translational modification which modulates the physical, chemical and biological properties of proteins. Glycosylation is important to monitor in both disease… (more)

Subjects/Keywords: biotherapeutics; capillary electrophoresis; glycans; mass spectrometry; Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Berger, V. L. (2013). Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003114

Chicago Manual of Style (16th Edition):

Berger, Victoria Lee. “Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry.” 2013. Masters Thesis, Northeastern University. Accessed February 25, 2020. http://hdl.handle.net/2047/d20003114.

MLA Handbook (7th Edition):

Berger, Victoria Lee. “Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry.” 2013. Web. 25 Feb 2020.

Vancouver:

Berger VL. Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 25]. Available from: http://hdl.handle.net/2047/d20003114.

Council of Science Editors:

Berger VL. Analysis of N-glycans released from proteins of therapeutic and clinical significance using capillary electrophoresis and liquid chromatography coupled to mass spectrometry. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003114


University of Kentucky

30. Jacobsen, Jesse M. TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS.

Degree: 2011, University of Kentucky

 Despite over a century of advancement, tuberculosis remains a grave threat to world health. In particular, third world countries continue to struggle with the crushing… (more)

Subjects/Keywords: Tuberculosis; Translocase I; Capuramycin; Total Synthesis; Medicinal Chemistry; Medicinal and Pharmaceutical Chemistry; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Jacobsen, J. M. (2011). TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/gradschool_theses/162

Chicago Manual of Style (16th Edition):

Jacobsen, Jesse M. “TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS.” 2011. Masters Thesis, University of Kentucky. Accessed February 25, 2020. http://uknowledge.uky.edu/gradschool_theses/162.

MLA Handbook (7th Edition):

Jacobsen, Jesse M. “TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS.” 2011. Web. 25 Feb 2020.

Vancouver:

Jacobsen JM. TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS. [Internet] [Masters thesis]. University of Kentucky; 2011. [cited 2020 Feb 25]. Available from: http://uknowledge.uky.edu/gradschool_theses/162.

Council of Science Editors:

Jacobsen JM. TOWARDS THE TOTAL SYNTHESIS OF THE CAPURAMYCIN FAMILY OF NATURAL PRODUCTS. [Masters Thesis]. University of Kentucky; 2011. Available from: http://uknowledge.uky.edu/gradschool_theses/162

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