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D-Alanine, D-alanyl-L-lysyl-3-cyclohexyl-L-alanyl-L-valyl-L-alanyl-L-alanyl-L-tryptophyl-L- threonyl-L-leucyl-L-lysyl-L-alanyl-L-alanyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194039-57-1

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  • D-Alanine, D-alanyl-L-lysyl-3-cyclohexyl-L-alanyl-L-valyl-L-alanyl-L-alanyl-L-tryptophyl-L- threonyl-L-leucyl-L-lysyl-L-alanyl-L-alanyl-

    Cas No: 194039-57-1

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194039-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194039-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,0,3 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 194039-57:
(8*1)+(7*9)+(6*4)+(5*0)+(4*3)+(3*9)+(2*5)+(1*7)=151
151 % 10 = 1
So 194039-57-1 is a valid CAS Registry Number.

194039-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name aKXAAWTLKAAa

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:194039-57-1 SDS

194039-57-1Downstream Products

194039-57-1Relevant articles and documents

Synthesis of a trimeric gp120 epitope mimic conjugated to a T-helper peptide to improve antigenicity

Schellinger, Joan G.,Danan-Leon, Lieza M.,Hoch, Jessica A.,Kassa, Aemro,Srivastava, Indresh,Davis, David,Gervay-Hague, Jacquelyn

, p. 3230 - 3233 (2011)

A fully synthetic trivalent mimotope of gp120 conjugated to pan allelic HLA DR binding epitope was prepared using solid-phase peptide synthesis and optimized copper-catalyzed azide-alkyne cycloaddition. The methodology efficiently provides chemically uniform heteromultimeric peptide constructs with enhanced binding, avidity, and specificity toward an established HIV-neutralizing human antibody, MAb b12. The versatile synthetic strategy serves as a powerful platform for the development of synthetic peptides as potential HIV-1 vaccine candidates.

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