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Title: Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy-D-gluco-homonojirimycin and N-butyl 1-deoxy-L-ido-homonojirimycin. Author: Markad SD, Karanjule NS, Sharma T, Sabharwal SG, Dhavale DD. Journal: Bioorg Med Chem; 2006 Aug 15; 14(16):5535-9. PubMed ID: 16682208. Abstract: Conjugate addition of n-butyl amine to d-glucose derived alpha,beta-unsaturated ester 4 afforded beta-amino esters 5a,b that on reduction of ester group, 1,2-acetonide deprotection, and reductive amination led to the formation of corresponding N-butyl 1-deoxy-D-gluco-homonojirimycin 2c and N-butyl 1-deoxy-L-ido-homonojirimycin 2d which were found to be selective beta-glucosidase inhibitors with an IC(50) value in millimolar range.[Abstract] [Full Text] [Related] [New Search]