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Journal of Medicinal Chemistry|April 21, 2007
Structure-guided optimization of small molecules inhibiting human immunodeficiency virus 1 Tat association with the human coactivator p300/CREB binding protein-associated factorChongfeng Pan, Mihaly Mezei, Shiraz Mujtaba, et al.Journal of Medicinal Chemistry|April 24, 2007
A high-throughput screen for aggregation-based inhibition in a large compound libraryBrian Y Feng, Anton Simeonov, Ajit Jadhav, et al.Journal of Medicinal Chemistry|April 24, 2007
Bispyridinium dienes: histone deacetylase inhibitors with selective activitiesCarlos Pérez-Balado, Angela Nebbioso, Paula Rodríguez-Graña, et al.Journal of Medicinal Chemistry|January 1, 1991
R and S enantiomers of 11-hydroxy- and 10,11-dihydroxy-N-allylnoraporphine: synthesis and affinity for dopamine receptors in rat brain tissueJ L Neumeyer, Y G Gao, N S Kula, et al.Journal of Medicinal Chemistry|January 1, 1991
trans-hexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol groupM P Seiler, A Hagenbach, H J Wüthrich, et al.Journal of Medicinal Chemistry|January 1, 1991
Synthesis of chiral and achiral pyranenamine derivatives. Potent agents with topical ocular antiallergic activityC Gluchowski, T E Bischoff, M E Garst, et al.Journal of Medicinal Chemistry|November 1, 1975
Hypo-beta-lipoproteinemic agents. 1. Bicyclo[2.2.2]octyloxyaniline and its derivativesC E Day, P E Schurr, D E Emmert, et al.Journal of Medicinal Chemistry|June 1, 1991
Lipophilic glycosyl phosphotriester derivatives of AZT: synthesis, NMR transmembrane transport study, and antiviral activityY Henin, C Gouyette, O Schwartz, et al.Journal of Medicinal Chemistry|March 1, 1991
Effect of fluorine substitution on the adrenergic properties of 3-(tert-butylamino)-1-(3,4-dihydroxyphenoxy)-2-propanolA Adejare, J Y Nie, D Hebel, et al.Journal of Medicinal Chemistry|March 1, 1991
Synthesis and biological evaluation of a series of substituted N-alkoxyimides and -amides as potential atypical antipsychotic agentsN J Hrib, J G Jurcak, F P Huger, et al.Pageof 3,134