Discovery of 1-(4-phenoxypiperidin-1-yl)-2-arylaminoethanone stearoyl-CoA desaturase 1 inhibitors
摘要:
A series of novel stearoyl-CoA desaturase 1 (SCD1) inhibitors were identified by scaffold design based on known SCD1 inhibitors. Large structural changes were made leading to multiple analogs with comparable or improved potency. This approach is valuable for generation of proprietary compounds without conducting a costly high-throughput screening. (c) 2007 Elsevier Ltd. All rights reserved.
[EN] PROCESS OF PREPARATION OF OPTICALLY ACTIVE ALPHA AMINOACETALS<br/>[FR] PRÉPARATION D'ALPHA AMINOCÉTALS OPTIQUEMENT ACTIFS
申请人:CLARIANT SPECIALTY FINE CHEM
公开号:WO2009106386A1
公开(公告)日:2009-09-03
The invention relates to a process for preparing optically active α-aminoacetals by resolution of a racemic mixture or of a mixture of enantiomers via the formation of diastereoisomeric salts, and also novel intermediates in the form of diastereoisomeric salts.
Composition containing a penem or carbapenem antibiotic
申请人:SANKYO COMPANY LIMITED
公开号:EP0178911A2
公开(公告)日:1986-04-23
57 Administration of an N-acylated amino acid (ornithine, lysine, phenylglycine or phenylalanine) in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. A pharmaceutical composition may be prepared simply by mixing the two components.