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Journal of Medicinal Chemistry|October 13, 1995
Synthesis of isoornithines and methylputrescines. An evaluation of their inhibitory effects on ornithine decarboxylaseG Aizencang, R B Frydman, S Giorgieri, et al.Journal of Medicinal Chemistry|October 27, 1995
Synthesis and structure-activity relationships of substituted 1,4-dihydroquinoxaline-2,3-diones: antagonists of N-methyl-D-aspartate (NMDA) receptor glycine sites and non-NMDA glutamate receptorsJ F Keana, S M Kher, S X Cai, et al.Journal of Medicinal Chemistry|October 27, 1995
The synthesis, structure-activity, and structure-side effect relationships of a series of 8-alkoxy- and 5-amino-8-alkoxyquinolone antibacterial agentsJ P Sanchez, R D Gogliotti, J M Domagala, et al.Journal of Medicinal Chemistry|October 27, 1995
Hypoxia-selective agents derived from 2-quinoxalinecarbonitrile 1,4-di-N-oxides. 2A Monge, F J Martínez-Crespo, A López de Ceráin, et al.Journal of Medicinal Chemistry|October 27, 1995
5-Arylthio-substituted 2-amino-4-oxo-6-methylpyrrolo[2,3-d]pyrimidine antifolates as thymidylate synthase inhibitors and antitumor agentsA Gangjee, R Devraj, J J McGuire, et al.Journal of Medicinal Chemistry|October 27, 1995
Thiopyranol[2,3,4-c,d]indoles as inhibitors of 5-lipoxygenase, 5-lipoxygenase-activating protein, and leukotriene C4 synthaseJ H Hutchinson, S Charleson, J F Evans, et al.Journal of Medicinal Chemistry|October 27, 1995
Y1 and Y2 receptor selective neuropeptide Y analogues: evidence for a Y1 receptor subclassD A Kirby, S C Koerber, J M May, et al.Journal of Medicinal Chemistry|November 10, 1995
A new series of pyridinone derivatives as potent non-nucleoside human immunodeficiency virus type 1 specific reverse transcriptase inhibitorsV Dollé, E Fan, C H Nguyen, et al.Journal of Medicinal Chemistry|November 10, 1995
Inhibition of the EGF-stimulated cellular proliferation of ER 22 cells by hydroxybiphenyl derivativesM E Million, J Boiziau, F Parker, et al.Journal of Medicinal Chemistry|November 10, 1995
Evidence for a carbocation intermediate during conversion of bipinnatin-A and -C into irreversible inhibitors of nicotinic acetylcholine receptorsE G Hyde, S M Thornhill, A J Boyer, et al.Pageof 3,141