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14 articles for MA Levy


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Structure-based design of cathepsin K inhibitors containing a benzyloxy-substituted benzoyl peptidomimetic.EBI
Smithkline Beecham Pharmaceuticals
Benzophenone- and indolecarboxylic acids: potent type-2 specific inhibitors of human steroid 5 alpha-reductase.EBI
Smithkline Beecham Pharmaceuticals
Steroidal A ring aryl carboxylic acids: a new class of steroid 5 alpha-reductase inhibitors.EBI
Smith Kline & French Laboratories
 
Design, synthesis and evaluation of dual domain FKBP ligandsEBI
TBA
 
A non-steroidal diene acid inhibitor of human type 2 stereoid 5-reductaseEBI
TBA
 
Preparative chiral HPLC separation of all possible stereoisomers of LY191704 and LY266111 and their in vitro inhibition of human types 1 and 2 steroid 5-reductasesEBI
TBA
 
The preparation and evaluation of (+/-)-trans-1-Diazo-8-methoxy-4a-methyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthren-2-one as an inhibitor of human type-1 steroid 5α-reductaseEBI
TBA
 
A comparison of steroidal and non-steroidal inhibitors of human steroid 5α-reductase: New tricyclic aryl acid inhibitors of the type-1 isozymeEBI
TBA
 
Synthesis and structure-activity relationships of macrocyclic FKBP ligandsEBI
TBA
 
Inhibition of steroid 5α-reductase by 3-nitrosteroids: synthesis, mechanism of inhibition, and in vivo activity.EBI
TBA
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin K.EBI
Smithkline Beecham Pharmaceuticals
Inhibition of steroid 5 alpha-reductase by unsaturated 3-carboxysteroids.EBI
Smith Kline & French Laboratories
Kinase inhibitorsBDB
Respivert
Inhibition of clinically relevant mutant variants of HIV-1 by quinazolinone non-nucleoside reverse transcriptase inhibitors.BDB
Dupont Pharmaceuticals