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10329-98-3

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  • N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-naphthalen-1-yloxyoxan-3-yl]acetamide CAS:10329-98-3 the cheapest price

    Cas No: 10329-98-3

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  • b-D-Glucopyranoside,1-naphthalenyl 2-(acetylamino)-2-deoxy-

    Cas No: 10329-98-3

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10329-98-3 Usage

Definition

ChEBI: An N-acetyl-beta-D-glucosaminide in which the anomeric hydroxy hydrogen is replaced by a 1-naphthyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 10329-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10329-98:
(7*1)+(6*0)+(5*3)+(4*2)+(3*9)+(2*9)+(1*8)=83
83 % 10 = 3
So 10329-98-3 is a valid CAS Registry Number.

10329-98-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-naphthalen-1-yloxyoxan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names HMS668D10

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10329-98-3 SDS

10329-98-3Downstream Products

10329-98-3Relevant articles and documents

Acceptor substrate-based selective inhibition of galactosyltransferases

Chung, Sang J.,Takayama, Shuichi,Wong, Chi-Huey

, p. 3359 - 3364 (1998)

This paper describes the discovery of glycosyl acceptor analogs as potent and selective inhibitors of α-1,3- and β-1,4- galactosyltransferases. Incorporation of an appropriate aromatic group to the aglycon position of the enzyme's acceptors results in a strong inhibition, representing the first and most potent small uncharged molecules as selective inhibitors of these two enzymes and thus providing a new strategy for the development of selective glycosyltransferase inhibitors.

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