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L-leucyl-L-phenylalanine methyl ester hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70691-56-4

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70691-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70691-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70691-56:
(7*7)+(6*0)+(5*6)+(4*9)+(3*1)+(2*5)+(1*6)=134
134 % 10 = 4
So 70691-56-4 is a valid CAS Registry Number.

70691-56-4SDS

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 L-leucyl-L-phenylalanine methyl ester hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-benzyl 2-((S)-2-amino-4-methylpentanamido)-3-phenylpropanoate hydrochloride

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:70691-56-4 SDS

70691-56-4Relevant academic research and scientific papers

Synthesis of a novel series of L-isoserine derivatives as aminopeptidase N inhibitors

Yang, Kanghui,Fen, Jinghong,Fang, Hao,Zhang, Lei,Gong, Jianzhi,Xu, Wenfang

, p. 302 - 310 (2012/07/02)

A series of novel L-isoserine derivatives were synthesised and evaluated for their ability to inhibit aminopeptidase N (APN)/CD13. In our preliminary biological results, some of these compounds possessed a potent inhibitory activity against the APN. Within this series, compound 14b not only showed similar enzyme inhibition (IC50 of 12.2μM) compared with the positive control bestatin (half maximal inhibitory concentration (IC 50) of 7.3μM), but also had a potent antiproliferative activity against human cancer cell lines cells.

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