Title : Microbial hydroxylation of pregnenolone derivatives - Choudhary_2005_Chem.Pharm.Bull.(Tokyo)_53_1455 |
Author(s) : Choudhary MI , Batool I , Shah SA , Nawaz SA , Atta ur R |
Ref : Chem Pharm Bull (Tokyo) , 53 :1455 , 2005 |
Abstract :
Pregnenolone and pregnenolone acetate were incubated with the fungi Cunninghamella elegans, Rhizopus stolonifer and Gibberella fujikuroi. Incubation of with C. elegans yielded metabolites, 3beta,7beta,11alpha-trihydroxypreg-5-en-20-one, 3beta,6alpha,11alpha,12beta,15beta-pentahydroxypreg-4-en-20-one and 3beta,6beta,11alpha-trihydroxypreg-4-en-20-one, while incubation with G. fujikuroi yielded two known metabolites, 3beta,7beta-dihydroxypregn-5-en-20-one and 6beta,15beta-dihydroxypreg-4-ene-3,20-dione. Metabolites and were found to be new. Fermentation of by C. elegans yielded four known oxidative metabolites, androsta-1,4-diene-3,17-dione, 6beta,15beta-dihydroxyandrost-4-ene-3,17-dione and 11alpha,15beta-dihydroxypreg-4-ene-3,20-dione. Fermentation of with R. stolonifer yielded two known metabolites, 11alpha-hydroxypreg-4-ene-3,20-dione and. Compounds were screened for their cholinesterase inhibitory activity in a mechanism-based assay. |
PubMedSearch : Choudhary_2005_Chem.Pharm.Bull.(Tokyo)_53_1455 |
PubMedID: 16272731 |
Choudhary MI, Batool I, Shah SA, Nawaz SA, Atta ur R (2005)
Microbial hydroxylation of pregnenolone derivatives
Chem Pharm Bull (Tokyo)
53 :1455
Choudhary MI, Batool I, Shah SA, Nawaz SA, Atta ur R (2005)
Chem Pharm Bull (Tokyo)
53 :1455