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Yazhong Huang

Showing results (1-10 of 11) with videos related to

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Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Novel dihydropyrazine analogues as NPY antagonistsSing-Yuen Sit, Yazhong Huang, Ildiko Antal-Zimanyi, et al.
Bioorganic & Medicinal Chemistry|February 27, 2016
Structure activity relationship studies on chemically non-reactive glycine sulfonamide inhibitors of diacylglycerol lipaseLouis S Chupak, Xiaofan Zheng, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry Letters|October 1, 2008
Preliminary SAR studies on non-apamin-displacing 4-(aminomethylaryl)pyrrazolopyrimidine K(Ca) channel blockersRobert G Gentles, Shuanghua Hu, Yazhong Huang, et al.
Bioorganic & Medicinal Chemistry Letters|September 9, 2008
Initial SAR studies on apamin-displacing 2-aminothiazole blockers of calcium-activated small conductance potassium channelsRobert G Gentles, Katherine Grant-Young, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry Letters|June 4, 2013
Heterocyclic modification of a novel bicyclo[3.1.0]hexane NPY1 receptor antagonistGuanglin Luo, Ling Chen, Shuanghua Hu, et al.
Journal of Medicinal Chemistry|October 31, 2003
Identification of a potent and selective 5-HT(6) antagonist: one-step synthesis of (E)-3-(benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from 2-(benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrileYong-Jin Wu, Huan He, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry|February 6, 2014
Structure activity relationship studies of 3-arylsulfonyl-pyrido[1,2-a]pyrimidin-4-imines as potent 5-HT₆ antagonistsShuanghua Hu, Yazhong Huang, Yong-Jin Wu, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a Novel Class of Bicyclo[3.1.0]hexanylpiperazines as Noncompetitive Neuropeptide Y Y1 AntagonistsShuanghua Hu, Yazhong Huang, Milind Deshpande, et al.
Science (New York, N.Y.)|September 13, 2021
A P(V) platform for oligonucleotide synthesisYazhong Huang, Kyle W Knouse, Shenjie Qiu, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 26, 2015
Discovery of D1 Dopamine Receptor Positive Allosteric Modulators: Characterization of Pharmacology and Identification of Residues that Regulate Species SelectivityMartin A Lewis, Lisa Hunihan, John Watson, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Novel dihydropyrazine analogues as NPY antagonistsSing-Yuen Sit, Yazhong Huang, Ildiko Antal-Zimanyi, et al.
Bioorganic & Medicinal Chemistry|February 27, 2016
Structure activity relationship studies on chemically non-reactive glycine sulfonamide inhibitors of diacylglycerol lipaseLouis S Chupak, Xiaofan Zheng, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry Letters|October 1, 2008
Preliminary SAR studies on non-apamin-displacing 4-(aminomethylaryl)pyrrazolopyrimidine K(Ca) channel blockersRobert G Gentles, Shuanghua Hu, Yazhong Huang, et al.
Bioorganic & Medicinal Chemistry Letters|September 9, 2008
Initial SAR studies on apamin-displacing 2-aminothiazole blockers of calcium-activated small conductance potassium channelsRobert G Gentles, Katherine Grant-Young, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry Letters|June 4, 2013
Heterocyclic modification of a novel bicyclo[3.1.0]hexane NPY1 receptor antagonistGuanglin Luo, Ling Chen, Shuanghua Hu, et al.
Journal of Medicinal Chemistry|October 31, 2003
Identification of a potent and selective 5-HT(6) antagonist: one-step synthesis of (E)-3-(benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from 2-(benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrileYong-Jin Wu, Huan He, Shuanghua Hu, et al.
Bioorganic & Medicinal Chemistry|February 6, 2014
Structure activity relationship studies of 3-arylsulfonyl-pyrido[1,2-a]pyrimidin-4-imines as potent 5-HT₆ antagonistsShuanghua Hu, Yazhong Huang, Yong-Jin Wu, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a Novel Class of Bicyclo[3.1.0]hexanylpiperazines as Noncompetitive Neuropeptide Y Y1 AntagonistsShuanghua Hu, Yazhong Huang, Milind Deshpande, et al.
Science (New York, N.Y.)|September 13, 2021
A P(V) platform for oligonucleotide synthesisYazhong Huang, Kyle W Knouse, Shenjie Qiu, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 26, 2015
Discovery of D1 Dopamine Receptor Positive Allosteric Modulators: Characterization of Pharmacology and Identification of Residues that Regulate Species SelectivityMartin A Lewis, Lisa Hunihan, John Watson, et al.
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