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101222-19-9

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101222-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101222-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101222-19:
(8*1)+(7*0)+(6*1)+(5*2)+(4*2)+(3*2)+(2*1)+(1*9)=49
49 % 10 = 9
So 101222-19-9 is a valid CAS Registry Number.

101222-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Valyl-L-valine benzyl 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:101222-19-9 SDS

101222-19-9Relevant articles and documents

Design, synthesis and evaluation of inhibitor of apoptosis protein (IAP) antagonists that are highly selective for the BIR2 domain of XIAP

Ardecky, Robert J.,Welsh, Kate,Finlay, Darren,Lee, Pooi San,González-López, Marcos,Ganji, Santhi Reddy,Ravanan, Palaniyandi,Mace, Peter D.,Riedl, Stefan J.,Vuori, Kristiina,Reed, John C.,Cosford, Nicholas D.P.

, p. 4253 - 4257 (2013/07/26)

We recently reported the systematic ligand-based rational design and synthesis of monovalent Smac mimetics that bind preferentially to the BIR2 domain of the anti-apoptotic protein XIAP. Expanded structure-activity relationship (SAR) studies around these peptidomimetics led to compounds with significantly improved selectivity (>60-fold) for the BIR2 domain versus the BIR3 domain of XIAP. The potent and highly selective IAP antagonist 8q (ML183) sensitized TRAIL-resistant prostate cancer cells to apoptotic cell death, highlighting the merit of this probe compound as a valuable tool to investigate the biology of XIAP.

Amino acids and peptides. XVII. Synthesis of peptides related to N-terminal portion of fibrin alpha-chain and their inhibitory effect on fibrinogen/thrombin clotting.

Kawasaki,Tsuji,Hirase,Miyano,Inouye,Iwamoto

, p. 525 - 528 (2007/10/02)

Various peptides related to N-terminal portion of fibrin alpha-chain were synthesized by the solution method and the solid-phase method, and their inhibitory effect on fibrinogen/thrombin clotting was examined. Extension of peptide chain from N-terminal t

Synthesis and structure-activity relationships of amastatin analogues, inhibitors of aminopeptidase A

Tobe,Morishima,Aoyagi,et al.

, p. 1865 - 1872 (2007/10/02)

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