Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Hegde

Showing results (151-160 of 168) with videos related to

Pageof 17
Sort By:
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists Part 1. The discovery of arylacetamides as viable replacements for the dihydropyrimidinone moiety of an HTS hitYu Jiang, Chien-An Chen, Kai Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 23, 2008
The novel neuropeptide Y Y5 receptor antagonist Lu AA33810 [N-[[trans-4-[(4,5-dihydro[1]benzothiepino[5,4-d]thiazol-2-yl)amino]cyclohexyl]methyl]-methanesulfonamide] exerts anxiolytic- and antidepressant-like effects in rat models of stress sensitivityMary W Walker, Toni D Wolinsky, Vrej Jubian, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists part 2: A hybrid strategy combining key fragments of HTS hitsChien-An Chen, Yu Jiang, Kai Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 24, 2007
Efficacy of the MCHR1 antagonist N-[3-(1-{[4-(3,4-difluorophenoxy)phenyl]methyl}(4-piperidyl))-4-methylphenyl]-2-methylpropanamide (SNAP 94847) in mouse models of anxiety and depression following acute and chronic administration is independent of hippocampal neurogenesisD J David, K C Klemenhagen, K A Holick, et al.
Pharmaceutics|November 11, 2022
Ileocolonic-Targeted JAK Inhibitor: A Safer and More Effective Treatment for Inflammatory Bowel DiseaseVipul Yadav, Aileen House, Silvia Matiz, et al.
Journal of Medicinal Chemistry|July 14, 2025
Discovery of ZN-c5, an Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) with Improved PharmacokineticsSayee G Hegde, Peter Q Huang, Kevin D Bunker, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 29, 2021
Characterization of the Onset, Progression, and Reversibility of Morphological Changes in Mouse Lung after Pharmacological Inhibition of Leucine-Rich Kinase 2 Kinase ActivityDianne K Bryce, Chris M Ware, Janice D Woodhouse, et al.
Pediatric Blood & Cancer|January 20, 2025
Cardiovascular Complications of Immune Effector Cell Therapies in Pediatric Hematological and Solid TumorsAaron B Ross, Kriti Puri, Thomas L Johnson, et al.
Physical Review Letters|October 22, 2021
Magnetic Field Induced Quantum Spin Liquid in the Two Coupled Trillium Lattices of K_{2}Ni_{2}(SO_{4})_{3}Ivica Živković, Virgile Favre, Catalina Salazar Mejia, et al.
Cells|May 13, 2026
uPAR-Targeting Cytotoxic Antibody-Drug Conjugates Selectively Deplete Proinflammatory Myeloid Cells for Autoimmune IndicationsHandan Xiang, Grace Pham Mortenson, Simon B Lang, et al.
Pageof 17

Showing results (151-160 of 168) with videos related to

Sort By:
Pageof 17
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists Part 1. The discovery of arylacetamides as viable replacements for the dihydropyrimidinone moiety of an HTS hitYu Jiang, Chien-An Chen, Kai Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 23, 2008
The novel neuropeptide Y Y5 receptor antagonist Lu AA33810 [N-[[trans-4-[(4,5-dihydro[1]benzothiepino[5,4-d]thiazol-2-yl)amino]cyclohexyl]methyl]-methanesulfonamide] exerts anxiolytic- and antidepressant-like effects in rat models of stress sensitivityMary W Walker, Toni D Wolinsky, Vrej Jubian, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists part 2: A hybrid strategy combining key fragments of HTS hitsChien-An Chen, Yu Jiang, Kai Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 24, 2007
Efficacy of the MCHR1 antagonist N-[3-(1-{[4-(3,4-difluorophenoxy)phenyl]methyl}(4-piperidyl))-4-methylphenyl]-2-methylpropanamide (SNAP 94847) in mouse models of anxiety and depression following acute and chronic administration is independent of hippocampal neurogenesisD J David, K C Klemenhagen, K A Holick, et al.
Pharmaceutics|November 11, 2022
Ileocolonic-Targeted JAK Inhibitor: A Safer and More Effective Treatment for Inflammatory Bowel DiseaseVipul Yadav, Aileen House, Silvia Matiz, et al.
Journal of Medicinal Chemistry|July 14, 2025
Discovery of ZN-c5, an Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) with Improved PharmacokineticsSayee G Hegde, Peter Q Huang, Kevin D Bunker, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 29, 2021
Characterization of the Onset, Progression, and Reversibility of Morphological Changes in Mouse Lung after Pharmacological Inhibition of Leucine-Rich Kinase 2 Kinase ActivityDianne K Bryce, Chris M Ware, Janice D Woodhouse, et al.
Pediatric Blood & Cancer|January 20, 2025
Cardiovascular Complications of Immune Effector Cell Therapies in Pediatric Hematological and Solid TumorsAaron B Ross, Kriti Puri, Thomas L Johnson, et al.
Physical Review Letters|October 22, 2021
Magnetic Field Induced Quantum Spin Liquid in the Two Coupled Trillium Lattices of K_{2}Ni_{2}(SO_{4})_{3}Ivica Živković, Virgile Favre, Catalina Salazar Mejia, et al.
Cells|May 13, 2026
uPAR-Targeting Cytotoxic Antibody-Drug Conjugates Selectively Deplete Proinflammatory Myeloid Cells for Autoimmune IndicationsHandan Xiang, Grace Pham Mortenson, Simon B Lang, et al.
Pageof 17