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Inkyu Hwang

Showing results (41-50 of 63) with videos related to

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Bioorganic & Medicinal Chemistry|September 18, 2003
Design, synthesis and biological evaluation of 10-CF3CO-DDACTHF analogues and derivatives as inhibitors of GAR Tfase and the de novo purine biosynthetic pathwayJoel Desharnais, Inkyu Hwang, Yan Zhang, et al.
Tetrahedron|February 18, 2010
Synthesis and Preliminary Evaluation of Duocarmycin Analogues Incorporating the 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[2,3-e]indol-4-one (CNI) and 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[1,2-e]indol-4-one (iso-CNI) Alkylation SubunitsCarla M Gauss, Akiyuki Hamasaki, Jay P Parrish, et al.
Journal of Ethnopharmacology|September 26, 2017
Anti-allergic effects of the ethanol extract of Syzygium formosum (Wall.) Masam leaves and its immunoregulatory mechanismsThi Minh Nguyet Nguyen, Maria Lomunova, Thi Phuong Duyen Vu, et al.
Journal of the American Chemical Society|March 19, 2009
Total synthesis of vinblastine, vincristine, related natural products, and key structural analoguesHayato Ishikawa, David A Colby, Shigeki Seto, et al.
Journal of the American Chemical Society|April 2, 2009
Design, synthesis, and evaluation of an alpha-helix mimetic library targeting protein-protein interactionsAlex Shaginian, Landon R Whitby, Sukwon Hong, et al.
Journal of Medicinal Chemistry|June 15, 2007
Structure-activity relationships of alpha-ketooxazole inhibitors of fatty acid amide hydrolaseChristophe Hardouin, Michael J Kelso, F Anthony Romero, et al.
Journal of Medicinal Chemistry|February 6, 2008
Optimization of alpha-ketooxazole inhibitors of fatty acid amide hydrolaseF Scott Kimball, F Anthony Romero, Cyrine Ezzili, et al.
Bioorganic & Medicinal Chemistry|April 26, 2005
Synthesis and biological evaluation of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid as a potential inhibitor of GAR Tfase and the de novo purine biosynthetic pathwayHeng Cheng, Inkyu Hwang, Youhoon Chong, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2009
Synthesis and evaluation of a thio analogue of duocarmycin SAKaren S MacMillan, James P Lajiness, Carlota Lopez Cara, et al.
Journal of the American Chemical Society|November 21, 2007
A unique class of duocarmycin and CC-1065 analogues subject to reductive activationWei Jin, John D Trzupek, Thomas J Rayl, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Bioorganic & Medicinal Chemistry|September 18, 2003
Design, synthesis and biological evaluation of 10-CF3CO-DDACTHF analogues and derivatives as inhibitors of GAR Tfase and the de novo purine biosynthetic pathwayJoel Desharnais, Inkyu Hwang, Yan Zhang, et al.
Tetrahedron|February 18, 2010
Synthesis and Preliminary Evaluation of Duocarmycin Analogues Incorporating the 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[2,3-e]indol-4-one (CNI) and 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[1,2-e]indol-4-one (iso-CNI) Alkylation SubunitsCarla M Gauss, Akiyuki Hamasaki, Jay P Parrish, et al.
Journal of Ethnopharmacology|September 26, 2017
Anti-allergic effects of the ethanol extract of Syzygium formosum (Wall.) Masam leaves and its immunoregulatory mechanismsThi Minh Nguyet Nguyen, Maria Lomunova, Thi Phuong Duyen Vu, et al.
Journal of the American Chemical Society|March 19, 2009
Total synthesis of vinblastine, vincristine, related natural products, and key structural analoguesHayato Ishikawa, David A Colby, Shigeki Seto, et al.
Journal of the American Chemical Society|April 2, 2009
Design, synthesis, and evaluation of an alpha-helix mimetic library targeting protein-protein interactionsAlex Shaginian, Landon R Whitby, Sukwon Hong, et al.
Journal of Medicinal Chemistry|June 15, 2007
Structure-activity relationships of alpha-ketooxazole inhibitors of fatty acid amide hydrolaseChristophe Hardouin, Michael J Kelso, F Anthony Romero, et al.
Journal of Medicinal Chemistry|February 6, 2008
Optimization of alpha-ketooxazole inhibitors of fatty acid amide hydrolaseF Scott Kimball, F Anthony Romero, Cyrine Ezzili, et al.
Bioorganic & Medicinal Chemistry|April 26, 2005
Synthesis and biological evaluation of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid as a potential inhibitor of GAR Tfase and the de novo purine biosynthetic pathwayHeng Cheng, Inkyu Hwang, Youhoon Chong, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2009
Synthesis and evaluation of a thio analogue of duocarmycin SAKaren S MacMillan, James P Lajiness, Carlota Lopez Cara, et al.
Journal of the American Chemical Society|November 21, 2007
A unique class of duocarmycin and CC-1065 analogues subject to reductive activationWei Jin, John D Trzupek, Thomas J Rayl, et al.
Pageof 7