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Showing results (21-30 of 39) with videos related to

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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.
Journal of the American Chemical Society|February 21, 2015
Ligand-enabled β-C-H arylation of α-amino acids using a simple and practical auxiliaryGang Chen, Toshihiko Shigenari, Pankaj Jain, 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.
Bioorganic & Medicinal Chemistry Letters|November 23, 2017
The discovery and optimization of naphthalene-linked P2-P4 Macrocycles as inhibitors of HCV NS3 proteaseMichael Bowsher, Sheldon Hiebert, Rongti Li, et al.
Current Drug Targets. Infectious Disorders|March 16, 2006
Developments in antiviral drug design, discovery and development in 2004Nicholas A Meanwell, Makonen Belema, David J Carini, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 23, 2017
The STAT4/MLL1 Epigenetic Axis Regulates the Antimicrobial Functions of Murine MacrophagesWilliam F Carson, Karen A Cavassani, Elyara M Soares, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2017
Functionalized triazines as potent HCV entry inhibitorsEric S Mull, Li-Qiang Sun, Qian Zhao, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacyGene M Dubowchik, Jodi A Michne, Dmitry Zuev, et al.
Bioorganic & Medicinal Chemistry Letters|December 25, 2016
Structure-activity relationships of 4-hydroxy-4-biaryl-proline acylsulfonamide tripeptides: A series of potent NS3 protease inhibitors for the treatment of hepatitis C virusAlan Xiangdong Wang, Jie Chen, Qian Zhao, et al.
Angewandte Chemie (International Ed. in English)|September 14, 2018
A General Amino Acid Synthesis Enabled by Innate Radical Cross-CouplingShengyang Ni, Alberto F Garrido-Castro, Rohan R Merchant, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
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.
Journal of the American Chemical Society|February 21, 2015
Ligand-enabled β-C-H arylation of α-amino acids using a simple and practical auxiliaryGang Chen, Toshihiko Shigenari, Pankaj Jain, 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.
Bioorganic & Medicinal Chemistry Letters|November 23, 2017
The discovery and optimization of naphthalene-linked P2-P4 Macrocycles as inhibitors of HCV NS3 proteaseMichael Bowsher, Sheldon Hiebert, Rongti Li, et al.
Current Drug Targets. Infectious Disorders|March 16, 2006
Developments in antiviral drug design, discovery and development in 2004Nicholas A Meanwell, Makonen Belema, David J Carini, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 23, 2017
The STAT4/MLL1 Epigenetic Axis Regulates the Antimicrobial Functions of Murine MacrophagesWilliam F Carson, Karen A Cavassani, Elyara M Soares, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2017
Functionalized triazines as potent HCV entry inhibitorsEric S Mull, Li-Qiang Sun, Qian Zhao, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacyGene M Dubowchik, Jodi A Michne, Dmitry Zuev, et al.
Bioorganic & Medicinal Chemistry Letters|December 25, 2016
Structure-activity relationships of 4-hydroxy-4-biaryl-proline acylsulfonamide tripeptides: A series of potent NS3 protease inhibitors for the treatment of hepatitis C virusAlan Xiangdong Wang, Jie Chen, Qian Zhao, et al.
Angewandte Chemie (International Ed. in English)|September 14, 2018
A General Amino Acid Synthesis Enabled by Innate Radical Cross-CouplingShengyang Ni, Alberto F Garrido-Castro, Rohan R Merchant, et al.
Pageof 4