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Ramkumar Rajamani

Showing results (11-20 of 33) with videos related to

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Chembiochem : a European Journal of Chemical Biology|March 19, 2005
Homology modeling and molecular dynamics simulations of the mu opioid receptor in a membrane-aqueous systemYan Zhang, Yuk Y Sham, Ramkumar Rajamani, et al.
Journal of Molecular Graphics & Modelling|November 19, 2005
Linear interaction energy models for beta-secretase (BACE) inhibitors: Role of van der Waals, electrostatic, and continuum-solvation termsBrett A Tounge, Ramkumar Rajamani, Ellen W Baxter, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2016
Discovery of furo[2,3-d][1,3]thiazinamines as beta amyloid cleaving enzyme-1 (BACE1) inhibitorsYong-Jin Wu, Jason Guernon, Ramkumar Rajamani, et al.
Molecular Pharmacology|June 25, 2017
A Functional Na<sub>V</sub>1.7-Na<sub>V</sub>Ab Chimera with a Reconstituted High-Affinity ProTx-II Binding SiteRamkumar Rajamani, Sophie Wu, Iyoncy Rodrigo, 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.
Bioorganic & Medicinal Chemistry Letters|January 15, 2019
Discovery of new indole-based acylsulfonamide Na<sub>v</sub>1.7 inhibitorsYong-Jin Wu, Brian Venables, Jason Guernon, et al.
Journal of Medicinal Chemistry|August 26, 2016
Discovery of S3-Truncated, C-6 Heteroaryl Substituted Aminothiazine β-Site APP Cleaving Enzyme-1 (BACE1) InhibitorsYong-Jin Wu, Jason Guernon, Jianliang Shi, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2018
Discovery of morpholine-based aryl sulfonamides as Na<sub>v</sub>1.7 inhibitorsYong-Jin Wu, Jason Guernon, Andrea McClure, 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.
ACS Medicinal Chemistry Letters|March 18, 2016
Targeting the BACE1 Active Site Flap Leads to a Potent Inhibitor That Elicits Robust Brain Aβ Reduction in RodentsYong-Jin Wu, Jason Guernon, Fukang Yang, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Chembiochem : a European Journal of Chemical Biology|March 19, 2005
Homology modeling and molecular dynamics simulations of the mu opioid receptor in a membrane-aqueous systemYan Zhang, Yuk Y Sham, Ramkumar Rajamani, et al.
Journal of Molecular Graphics & Modelling|November 19, 2005
Linear interaction energy models for beta-secretase (BACE) inhibitors: Role of van der Waals, electrostatic, and continuum-solvation termsBrett A Tounge, Ramkumar Rajamani, Ellen W Baxter, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2016
Discovery of furo[2,3-d][1,3]thiazinamines as beta amyloid cleaving enzyme-1 (BACE1) inhibitorsYong-Jin Wu, Jason Guernon, Ramkumar Rajamani, et al.
Molecular Pharmacology|June 25, 2017
A Functional Na<sub>V</sub>1.7-Na<sub>V</sub>Ab Chimera with a Reconstituted High-Affinity ProTx-II Binding SiteRamkumar Rajamani, Sophie Wu, Iyoncy Rodrigo, 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.
Bioorganic & Medicinal Chemistry Letters|January 15, 2019
Discovery of new indole-based acylsulfonamide Na<sub>v</sub>1.7 inhibitorsYong-Jin Wu, Brian Venables, Jason Guernon, et al.
Journal of Medicinal Chemistry|August 26, 2016
Discovery of S3-Truncated, C-6 Heteroaryl Substituted Aminothiazine β-Site APP Cleaving Enzyme-1 (BACE1) InhibitorsYong-Jin Wu, Jason Guernon, Jianliang Shi, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2018
Discovery of morpholine-based aryl sulfonamides as Na<sub>v</sub>1.7 inhibitorsYong-Jin Wu, Jason Guernon, Andrea McClure, 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.
ACS Medicinal Chemistry Letters|March 18, 2016
Targeting the BACE1 Active Site Flap Leads to a Potent Inhibitor That Elicits Robust Brain Aβ Reduction in RodentsYong-Jin Wu, Jason Guernon, Fukang Yang, et al.
Pageof 4