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3-Oxa-5,9,11-triazatridecan-13-oic acid, 7-hydroxy-2,2,12-trimethyl-4,10-dioxo-6,9-bis(phenylmethyl)-, methyl ester, (6R,7R,12R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853904-91-3

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853904-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853904-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,9,0 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 853904-91:
(8*8)+(7*5)+(6*3)+(5*9)+(4*0)+(3*4)+(2*9)+(1*1)=193
193 % 10 = 3
So 853904-91-3 is a valid CAS Registry Number.

853904-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-[3-Benzyl-3-((2R,3R)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butyl)-ureido]-propionic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

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:853904-91-3 SDS

853904-91-3Downstream Products

853904-91-3Relevant academic research and scientific papers

Stereochemical analysis of (hydroxyethyl)urea peptidomimetic inhibitors of γ-secretase

Bakshi, Pancham,Wolfe, Michael S.

, p. 6485 - 6489 (2007/10/03)

(Hydroxyethyl)urea peptidomimetics systematically altered at positions P2-P3′ with hydrophobic D-amino acids were synthesized. An all D-amino acid containing analogue was identified that effectively blocked γ-secretase activity in a cell-free system (IC50 = 30 nM). Systematic alteration of the stereocenters of a potent compound revealed interdependence between the various positions. Although typically less potent than their L-peptidomimetic counterparts, selected all D-amino acid containing analogues were equipotent to their counterparts in a cell-based assay when incubated for extended times.

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