Bioorganic & Medicinal Chemistry 2006-08-15

Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy-D-gluco-homonojirimycin and N-butyl 1-deoxy-L-ido-homonojirimycin.

Shankar D Markad, Narayan S Karanjule, Tarun Sharma, Sushma G Sabharwal, Dilip D Dhavale

Index: Bioorg. Med. Chem. 14(16) , 5535-9, (2006)

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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.

Related Compounds

  • a-Homonojirimycin

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