Alpha-mannosidase and fucosidase inhibitors
First Claim
1. A composition comprising a compound of the formula ##STR7## wherein R is a (C1 -C6)alkyl optionally substituted with one or two hydroxy groups, a glycosyl group, a group of the formula --(CH2)n --Ar, wherein n is an integer of from 1 to 4 and Ar is a phenyl optionally substituted with one or two groups selected from (C1 -C4)alkyl, (C1 -C4)alkoxy, fluoro, chloro, bromo, iodo, amino, mono(C1 -C4)alkylamino or di(C1 -C4)alkylamino, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
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Accused Products
Abstract
Substituted (1α,2β,3α or β,4α,5α or β)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclopentylamines are inhibitors of alpha-mannosidase and alpha-fucosidase and are useful immunostimulants, antiviral and antimetastatic agents.
6 Citations
1 Claim
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1. A composition comprising a compound of the formula ##STR7## wherein R is a (C1 -C6)alkyl optionally substituted with one or two hydroxy groups, a glycosyl group, a group of the formula --(CH2)n --Ar, wherein n is an integer of from 1 to 4 and Ar is a phenyl optionally substituted with one or two groups selected from (C1 -C4)alkyl, (C1 -C4)alkoxy, fluoro, chloro, bromo, iodo, amino, mono(C1 -C4)alkylamino or di(C1 -C4)alkylamino, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
Specification