Showing results (1891-1900 of 31,409) with videos related to
Sort By:
Pageof 3,141
Journal of Medicinal Chemistry|November 2, 1999
Synthesis of novel GABA uptake inhibitors. 4. Bioisosteric transformation and successive optimization of known GABA uptake inhibitors leading to a series of potent anticonvulsant drug candidatesK E Andersen, J L Sørensen, P O Huusfeldt, et al.Journal of Medicinal Chemistry|November 2, 1999
Structure-activity relationships and molecular modeling analysis of flavonoids binding to the benzodiazepine site of the rat brain GABA(A) receptor complexK Dekermendjian, P Kahnberg, M R Witt, et al.Journal of Medicinal Chemistry|January 14, 2000
Isoxazolines as potent antagonists of the integrin alpha(v)beta(3)W J Pitts, J Wityak, J M Smallheer, et al.Journal of Medicinal Chemistry|January 14, 2000
Synthesis and opioid receptor affinity of morphinan and benzomorphan derivatives: mixed kappa agonists and mu agonists/antagonists as potential pharmacotherapeutics for cocaine dependenceJ L Neumeyer, J M Bidlack, R Zong, et al.Journal of Medicinal Chemistry|April 1, 1976
Synthesis and biological activities of some N4-substituted 4-aminopyrazolo(3,4-d)pyrimidinesC I Hong, N C De, G L Tritsch, et al.Journal of Medicinal Chemistry|November 2, 1999
Pyrroloquinoxaline derivatives as high-affinity and selective 5-HT(3) receptor agonists: synthesis, further structure-activity relationships, and biological studiesG Campiani, E Morelli, S Gemma, et al.Journal of Medicinal Chemistry|January 1, 1975
Purinylhydantoins. Facile conversion of the naturally occurring N-(purin-6-ylcarbamoyl)-L-amino acids into 3-pruin-6-ylhydantoins and 3-cyclohexyl-1-(purin-6-ylcarbamoyl)hydantoinsC I Hong, G B ChhedaJournal of Medicinal Chemistry|April 10, 1999
Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone seriesY Song, D T Connor, R Doubleday, et al.Journal of Medicinal Chemistry|April 10, 1999
Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1,3,4- and 1,2,4-thiadiazole seriesY Song, D T Connor, A D Sercel, et al.Journal of Medicinal Chemistry|May 7, 1999
SQ: a program for rapidly producing pharmacophorically relevent molecular superpositionsM D Miller, R P Sheridan, S K KearsleyPageof 3,141