Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Medicinal Pharmaceutical Chemistry). Showing records 1 – 30 of 386 total matches.

[1] [2] [3] [4] [5] … [13]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Country

▼ Search Limiters


Duquesne University

1. Choudhary, Shruti. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.

Degree: PhD, Medicinal Chemistry, 2017, Duquesne University

  Dose limiting toxicity and development of multidrug resistance by the tumors are the major limitations of current cancer chemotherapy. Microtubule targeting agents (MTAs) are… (more)

Subjects/Keywords: Medicinal-Pharmaceutical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Choudhary, S. (2017). Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/233

Chicago Manual of Style (16th Edition):

Choudhary, Shruti. “Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 15, 2021. https://dsc.duq.edu/etd/233.

MLA Handbook (7th Edition):

Choudhary, Shruti. “Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Web. 15 Apr 2021.

Vancouver:

Choudhary S. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2021 Apr 15]. Available from: https://dsc.duq.edu/etd/233.

Council of Science Editors:

Choudhary S. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/233


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Johnston MR. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2021 Apr 15]. 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

3. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://hdl.handle.net/1808/21649.

MLA Handbook (7th Edition):

Mishra, Sanket J. “Structure-Based Design of Grp94-Selective Inhibitors.” 2014. Web. 15 Apr 2021.

Vancouver:

Mishra SJ. Structure-Based Design of Grp94-Selective Inhibitors. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2021 Apr 15]. 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

4. Alshehri, Saad Ali. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.

Degree: PhD, Chemistry and Biochemistry, 2020, South Dakota State University

  Diabetes mellitus (DM) is a metabolic disease characterized by high levels of blood glucose resulting from defects in insulin production or action. A world-wide… (more)

Subjects/Keywords: Chemistry; Medicinal-Pharmaceutical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Alshehri, S. A. (2020). Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. (Doctoral Dissertation). South Dakota State University. Retrieved from https://openprairie.sdstate.edu/etd/4101

Chicago Manual of Style (16th Edition):

Alshehri, Saad Ali. “Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.” 2020. Doctoral Dissertation, South Dakota State University. Accessed April 15, 2021. https://openprairie.sdstate.edu/etd/4101.

MLA Handbook (7th Edition):

Alshehri, Saad Ali. “Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.” 2020. Web. 15 Apr 2021.

Vancouver:

Alshehri SA. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. [Internet] [Doctoral dissertation]. South Dakota State University; 2020. [cited 2021 Apr 15]. Available from: https://openprairie.sdstate.edu/etd/4101.

Council of Science Editors:

Alshehri SA. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. [Doctoral Dissertation]. South Dakota State University; 2020. Available from: https://openprairie.sdstate.edu/etd/4101


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Raborg T. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. [Internet] [Thesis]. Virginia Commonwealth University; 2014. [cited 2021 Apr 15]. 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


University of Washington

6. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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


Duquesne University

7. Shah, Khushbu. Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection.

Degree: PhD, Medicinal Chemistry, 2017, Duquesne University

  This dissertation describes an introduction, background and research progress in the areas of agents designed as (a) selective Pneumocystis jirovecii dihydrofolate reductase (pjDHFR) inhibitors… (more)

Subjects/Keywords: Medicinal and Pharmaceutical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shah, K. (2017). Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/234

Chicago Manual of Style (16th Edition):

Shah, Khushbu. “Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 15, 2021. https://dsc.duq.edu/etd/234.

MLA Handbook (7th Edition):

Shah, Khushbu. “Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Web. 15 Apr 2021.

Vancouver:

Shah K. Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2021 Apr 15]. Available from: https://dsc.duq.edu/etd/234.

Council of Science Editors:

Shah K. Target Based Design and Synthesis of Fused Pyrimidines in the Potential Treatment of Cancer and Opportunistic Infection. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/234


McMaster University

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Edem P. PREPARATION AND EVALUATION OF PEPTIDYL ACYLOXYMETHYL KETONES FOR CATHEPSIN B IMAGING. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2021 Apr 15]. 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

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

Degree: MSin 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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


Michigan Technological University

10. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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 Arkansas

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Roberts JL. Green Chemistry Oxidative Modification of Peptoids Utilizing Bleach and TEMPO. [Internet] [Masters thesis]. University of Arkansas; 2017. [cited 2021 Apr 15]. 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


University of Montana

12. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. https://scholarworks.umt.edu/etd/11491.

MLA Handbook (7th Edition):

Gutierrez, Mathew M. “XFlow: An algorithm for extracting ion chromatograms.” 2019. Web. 15 Apr 2021.

Vancouver:

Gutierrez MM. XFlow: An algorithm for extracting ion chromatograms. [Internet] [Masters thesis]. University of Montana; 2019. [cited 2021 Apr 15]. 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

13. Pandey, Pankaj. Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators.

Degree: PhD, Biomolecular Sciences, 2015, University of Mississippi

  The cannabinoid receptors (CB1 and CB2) belong to the family of class A GPCRs. The CB1 receptor is predominately found in the central nervous… (more)

Subjects/Keywords: Computational Medicinal Chemistry; Medicinal Chemistry; Pharmacy and Pharmaceutical Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pandey, P. (2015). Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/1465

Chicago Manual of Style (16th Edition):

Pandey, Pankaj. “Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators.” 2015. Doctoral Dissertation, University of Mississippi. Accessed April 15, 2021. https://egrove.olemiss.edu/etd/1465.

MLA Handbook (7th Edition):

Pandey, Pankaj. “Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators.” 2015. Web. 15 Apr 2021.

Vancouver:

Pandey P. Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators. [Internet] [Doctoral dissertation]. University of Mississippi; 2015. [cited 2021 Apr 15]. Available from: https://egrove.olemiss.edu/etd/1465.

Council of Science Editors:

Pandey P. Protein-ligand interaction studies and identification of new drug-like hits as cannabinoid receptor modulators. [Doctoral Dissertation]. University of Mississippi; 2015. Available from: https://egrove.olemiss.edu/etd/1465


Temple University

14. 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;

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://digital.library.temple.edu/u?/p245801coll10,232219.

MLA Handbook (7th Edition):

Gao, Rong. “DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS.” 2013. Web. 15 Apr 2021.

Vancouver:

Gao R. DESIGN, SYNTHESIS AND EVALUATION OF NOVEL MUSCARINIC LIGANDS. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2021 Apr 15]. 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

15. 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;

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

16. Alsharif, Walid. Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction.

Degree: PhD, Biomolecular Sciences, 2015, University of Mississippi

 Sigma receptors are a well-defined unique class of receptors and are highly expressed in the central nervous system and also widely distributed in peripheral organs… (more)

Subjects/Keywords: Medicinal Chemistry; Pharmacy and Pharmaceutical Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Alsharif, W. (2015). Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/1454

Chicago Manual of Style (16th Edition):

Alsharif, Walid. “Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction.” 2015. Doctoral Dissertation, University of Mississippi. Accessed April 15, 2021. https://egrove.olemiss.edu/etd/1454.

MLA Handbook (7th Edition):

Alsharif, Walid. “Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction.” 2015. Web. 15 Apr 2021.

Vancouver:

Alsharif W. Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction. [Internet] [Doctoral dissertation]. University of Mississippi; 2015. [cited 2021 Apr 15]. Available from: https://egrove.olemiss.edu/etd/1454.

Council of Science Editors:

Alsharif W. Design, synthesis, and biological evaluation of sigma receptors (σRS) ligands as potential pharmacotherapy for cancer and drug addiction. [Doctoral Dissertation]. University of Mississippi; 2015. Available from: https://egrove.olemiss.edu/etd/1454


University of Central Florida

17. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. https://stars.library.ucf.edu/etd/6107.

MLA Handbook (7th Edition):

Zhang, Li. “Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles.” 2004. Web. 15 Apr 2021.

Vancouver:

Zhang L. Block Copolymer Stabilized Self-Assembled Magnetic Nanoparticles. [Internet] [Masters thesis]. University of Central Florida; 2004. [cited 2021 Apr 15]. 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


Virginia Commonwealth University

18. Pendergrass, Heather A. Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus.

Degree: PhD, Pharmaceutical Sciences, 2020, Virginia Commonwealth University

  Antibiotics inhibit the growth or survival of bacteria by targeting their essential functions.1 Due to weaknesses in traditional antibiotics and the increasing prevalence of… (more)

Subjects/Keywords: Medicinal and Pharmaceutical Chemistry; Pathogenic Microbiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pendergrass, H. A. (2020). Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/6506

Chicago Manual of Style (16th Edition):

Pendergrass, Heather A. “Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus.” 2020. Doctoral Dissertation, Virginia Commonwealth University. Accessed April 15, 2021. https://scholarscompass.vcu.edu/etd/6506.

MLA Handbook (7th Edition):

Pendergrass, Heather A. “Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus.” 2020. Web. 15 Apr 2021.

Vancouver:

Pendergrass HA. Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2020. [cited 2021 Apr 15]. Available from: https://scholarscompass.vcu.edu/etd/6506.

Council of Science Editors:

Pendergrass HA. Development of a Screening Assay for Type III Secretion System Inhibitors and High Throughput Screening Campaign of Inhibitors of PRP of Staphylococcus aureus. [Doctoral Dissertation]. Virginia Commonwealth University; 2020. Available from: https://scholarscompass.vcu.edu/etd/6506


Northeastern University

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://hdl.handle.net/2047/d20001091.

MLA Handbook (7th Edition):

Kallmerten, Amy Elaine. “Microwave-accelerated transformations in synthetic organic & medicinal chemistry.” 2010. Web. 15 Apr 2021.

Vancouver:

Kallmerten AE. Microwave-accelerated transformations in synthetic organic & medicinal chemistry. [Internet] [Doctoral dissertation]. Northeastern University; 2010. [cited 2021 Apr 15]. 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

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Perera KLIS. Design and Synthesis of Selective Estrogen Receptor β Agonists and Their Pharmacology. [Internet] [Thesis]. Marquette University; 2017. [cited 2021 Apr 15]. 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

21. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Kozhushnyan AI. Rational design and synthesis of amplified therapeutic/diagnostic agents targeting the estrogen receptor. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2021 Apr 15]. 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


Western Kentucky University

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

24. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://scholarworks.umass.edu/theses/686.

MLA Handbook (7th Edition):

Holmes, Breanne E. “Selective Inhibition Studies of Factor Inhibiting Hif (fih).” 2011. Web. 15 Apr 2021.

Vancouver:

Holmes BE. Selective Inhibition Studies of Factor Inhibiting Hif (fih). [Internet] [Masters thesis]. U of Massachusetts : Masters; 2011. [cited 2021 Apr 15]. 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


Northeastern University

25. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

26. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://hdl.handle.net/2047/d20003111.

MLA Handbook (7th Edition):

Alexander, Abigail. “Expeditious routes of fluorinations: a comparative study.” 2013. Web. 15 Apr 2021.

Vancouver:

Alexander A. Expeditious routes of fluorinations: a comparative study. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2021 Apr 15]. 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

27. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

28. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. http://hdl.handle.net/2047/d20002789.

MLA Handbook (7th Edition):

Yin, Pengcheng. “Computational studies of enzyme function and dynamics.” 2012. Web. 15 Apr 2021.

Vancouver:

Yin P. Computational studies of enzyme function and dynamics. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2021 Apr 15]. 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

29. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

30. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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

[1] [2] [3] [4] [5] … [13]

.