CSIR Central

Aza-Annulation on the 16-dehydropregnenolone, via tandem intermolecular Aldol process and intramolecular Michael addition

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

View Archive Info
 
 
Field Value
 
Creator Kumar, Manmeet
Rawat, Preeti
Khan, M F
Rawat, A K
Srivastava, A K
Maurya, Rakesh
 
Date 2011-07-15T08:49:16Z
2011-07-15T08:49:16Z
2011
 
Identifier Bioorganic & Medicinal Chemistry Letters (2011), 21(8), 2232-37
http://hdl.handle.net/123456789/703
 
Description 16-Dehydropregnenolone undergoes a smooth annulation with propan-1-amine and aromatic aldehydes. Several amine derivatives of 16- dehydropregnenolone were synthesized and evaluated as inhibitors of DPP-IV. The structures of compounds were confirmed by 1H, 13C, NMR and mass spectral analysis. Among seventeen compounds evaluated only five compounds 1, 9, 13, 15 and 16 demonstrated significant inhibition of DPP. This study suggest that introduction of appropriate substituents in the 16-Dehydropregnenolone plays an important role in DPP-IV inhibitory activity.
 
Format 184892 bytes
application/pdf
 
Language en
 
Subject 16-Dehydropregnenolone
Annulation
DPP-IV
Gene
Cyclisation
 
Title Aza-Annulation on the 16-dehydropregnenolone, via tandem intermolecular Aldol process and intramolecular Michael addition
 
Type Article