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2-mercaptomethyl-5-guanidinopentanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69734-02-7

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69734-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69734-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,3 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69734-02:
(7*6)+(6*9)+(5*7)+(4*3)+(3*4)+(2*0)+(1*2)=157
157 % 10 = 7
So 69734-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N3O2S/c8-7(9)10-3-1-2-5(4-13)6(11)12/h5,13H,1-4H2,(H,11,12)(H4,8,9,10)

69734-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(diaminomethylideneamino)-2-(sulfanylmethyl)pentanoic acid

1.2 Other means of identification

Product number -
Other names 5-carbamimidamido-2-(sulfanylmethyl)pentanoic acid

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:69734-02-7 SDS

69734-02-7Downstream Products

69734-02-7Relevant academic research and scientific papers

Amino acid derivatives

-

, (2008/06/13)

A method for alleviating or reducing angiotensin related hypertension in hypertensive mammals comprises administering an effective amount of a compound having the general formula STR1 Intermediates for the preparation of such compounds are also included.

Design of potent and specific inhibitors of carboxypeptidases A and B.

Ondetti et al.

, p. 1427,1428 (2007/10/06)

The combination in one molecule of functional groups that can interact specifically with different substrate binding areas at the active site of carboxypeptidases A and B has led to the development of potent and specific inhibitors of these enzymes. 2-Benzyl-3-mercaptopropanoic acid (SQ 14,603) has a Ki of 1.1 x 10(-8) M vs. carboxypeptidase A and a Ki of 1.6 x 10(-4) M vs. the B enzyme. 2-Mercaptomethyl-5-guanidinopentanoic acid (SQ 24,798) has a Ki of 4 x 10(-10) M vs. carboxypeptidase B and a Ki of 1.2 x 10(-5) M vs. carboxypeptidase A. It is proposed that the sulfhydryl groups of these inhibitors bind to the catalytically important zinc ions of these enzymes, and that, in conjunction with the benzyl and guanidinopropyl side chains, they are responsible for their specificity.

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