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W Combs

Showing results (61-70 of 74) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|October 1, 1996
Induction of a novel conformation in the progesterone receptor by ZK299 involves a defined region of the carboxyl-terminal tailG F Allan, E Lombardi, D Haynes-Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|May 6, 2004
Synthesis and evaluation of spirobenzazepines as potent vasopressin receptor antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, et al.
Journal of Medicinal Chemistry|December 8, 1995
Nonsteroidal progesterone receptor ligands. 2. High-affinity ligands with selectivity for bone cell progesterone receptorsD W Combs, K Reese, L A Cornelius, et al.
Journal of Medicinal Chemistry|December 30, 2003
Benzoxazinones as PPARgamma agonists. 2. SAR of the amide substituent and in vivo results in a type 2 diabetes modelPhilip J Rybczynski, Roxanne E Zeck, Joseph Dudash, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2007
Discovery of selective imidazole-based inhibitors of mammalian 15-lipoxygenase: highly potent against human enzyme within a cellular environmentDavid S Weinstein, Wen Liu, Khehyong Ngu, et al.
Journal of Medicinal Chemistry|January 1, 1990
6-Benzoxazinylpyridazin-3-ones: potent, long-acting positive inotrope and peripheral vasodilator agentsD W Combs, M S Rampulla, S C Bell, et al.
Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Synthesis and evaluation of nonpeptide substituted spirobenzazepines as potent vasopressin antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, et al.
Beneficial Microbes|October 28, 2015
Calcium phosphate supplementation increases faecal Lactobacillus spp. in a randomised trial of young adultsW J Dahl, A L Ford, J A Coppola, et al.
Bioorganic & Medicinal Chemistry Letters|June 24, 2011
Pyrazole-based sulfonamide and sulfamides as potent inhibitors of mammalian 15-lipoxygenaseKhehyong Ngu, David S Weinstein, Wen Liu, et al.
Bioorganic & Medicinal Chemistry Letters|December 20, 2003
Aminoimidazoles as bioisosteres of acylguanidines: novel, potent, selective and orally bioavailable inhibitors of the sodium hydrogen exchanger isoform-1Saleem Ahmad, Khehyong Ngu, Donald W Combs, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Molecular Endocrinology (Baltimore, Md.)|October 1, 1996
Induction of a novel conformation in the progesterone receptor by ZK299 involves a defined region of the carboxyl-terminal tailG F Allan, E Lombardi, D Haynes-Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|May 6, 2004
Synthesis and evaluation of spirobenzazepines as potent vasopressin receptor antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, et al.
Journal of Medicinal Chemistry|December 8, 1995
Nonsteroidal progesterone receptor ligands. 2. High-affinity ligands with selectivity for bone cell progesterone receptorsD W Combs, K Reese, L A Cornelius, et al.
Journal of Medicinal Chemistry|December 30, 2003
Benzoxazinones as PPARgamma agonists. 2. SAR of the amide substituent and in vivo results in a type 2 diabetes modelPhilip J Rybczynski, Roxanne E Zeck, Joseph Dudash, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2007
Discovery of selective imidazole-based inhibitors of mammalian 15-lipoxygenase: highly potent against human enzyme within a cellular environmentDavid S Weinstein, Wen Liu, Khehyong Ngu, et al.
Journal of Medicinal Chemistry|January 1, 1990
6-Benzoxazinylpyridazin-3-ones: potent, long-acting positive inotrope and peripheral vasodilator agentsD W Combs, M S Rampulla, S C Bell, et al.
Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Synthesis and evaluation of nonpeptide substituted spirobenzazepines as potent vasopressin antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, et al.
Beneficial Microbes|October 28, 2015
Calcium phosphate supplementation increases faecal Lactobacillus spp. in a randomised trial of young adultsW J Dahl, A L Ford, J A Coppola, et al.
Bioorganic & Medicinal Chemistry Letters|June 24, 2011
Pyrazole-based sulfonamide and sulfamides as potent inhibitors of mammalian 15-lipoxygenaseKhehyong Ngu, David S Weinstein, Wen Liu, et al.
Bioorganic & Medicinal Chemistry Letters|December 20, 2003
Aminoimidazoles as bioisosteres of acylguanidines: novel, potent, selective and orally bioavailable inhibitors of the sodium hydrogen exchanger isoform-1Saleem Ahmad, Khehyong Ngu, Donald W Combs, et al.
Pageof 8