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L-Valine, N-L-phenylalanyl-, methyl ester, monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58173-46-9

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58173-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58173-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,7 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58173-46:
(7*5)+(6*8)+(5*1)+(4*7)+(3*3)+(2*4)+(1*6)=139
139 % 10 = 9
So 58173-46-9 is a valid CAS Registry Number.

58173-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name L-phenylalanyl-L-valine methyl ester hydrochloride

1.2 Other means of identification

Product number -
Other names Phe-Val-OMe*HCl

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:58173-46-9 SDS

58173-46-9Relevant academic research and scientific papers

Highly stereoselective synthesis of natural-product-like hybrids by an organocatalytic/multicomponent reaction sequence

Echemendía, Radell,De La Torre, Alexander F.,Monteiro, Julia L.,Pila, Michel,Corrêa, Arlene G.,Westermann, Bernhard,Rivera, Daniel G.,Paix?o, Márcio W.

, p. 7621 - 7625 (2015/06/25)

In an endeavor to provide an efficient route to natural product hybrids, described herein is an efficient, highly stereoselective, one-pot process comprising an organocatalytic conjugate addition of 1,3-dicarbonyls to α,β-unsaturated aldehydes followed by

Design, synthesis and biological evaluation of novel L-isoserine tripeptide derivatives as aminopeptidase N inhibitors

Pan, Huili,Yang, Kanghui,Zhang, Jian,Xu, Yingying,Jiang, Yuqi,Yuan, Yumei,Zhang, Xiaopan,Xu, Wenfang

, p. 717 - 726 (2013/07/26)

Aminopeptidase N (APN/CD13) is one of the essential proteins for tumour invasion, angiogenesis and metastasis as it is over-expressed on the surface of different tumour cells. Based on our previous work that L-isoserine dipeptide derivatives were potent APN inhibitors, we designed and synthesized L-isoserine tripeptide derivatives as APN inhibitors. Among these compounds, one compound 16l (IC50=2.51±0.2 M) showed similar inhibitory effect compared with control compound Bestatin (IC50=6.25±0.4 M) and it could be used as novel lead compound for the APN inhibitors development as anticancer agents in the future.

Synthesis and precursor-directed biosynthesis of new hormaomycin analogues

Zlatopolskiy, Boris D.,Radzom, Markus,Zeeck, Axel,De Meijere, Armin

, p. 1525 - 1534 (2007/10/03)

Several new analogues of hormaomycin (1), a peptide lactone with interesting biological activities, were prepared by total synthesis or by precursor-directed biosynthesis. The new analogues 2a-c, 3a-c, O-MOM-1 and epi-O-MOM-1 as well as the model acyl tri

Covalently bonded platinum(II) complexes of α-amino acids and peptides as a potential tool for protein labeling

Guillena, Gabriela,Rodriguez, Gema,Albrecht, Martin,Van Koten, Gerard

, p. 5368 - 5376 (2007/10/03)

Arylplatinum(II) complexes have been covalently bonded to the N and C termini and to the α-carbon of various amino acid derivatives. These organometallic-functionalized amino acid compounds can be converted into the corresponding free amino acids under bo

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