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Pyruvylglycine is a chemical compound that is formed as an intermediate in the metabolism of certain amino acids, particularly in the breakdown of leucine, isoleucine, and valine. It is a derivative of glycine, an amino acid, with a pyruvate group attached to it. Pyruvylglycine plays a crucial role in the tricarboxylic acid (TCA) cycle, also known as the Krebs cycle, which is a series of chemical reactions used by all aerobic organisms to generate energy through the oxidation of acetate derived from carbohydrates, fats, and proteins. In the TCA cycle, pyruvylglycine is converted into alanine, which is then further metabolized to produce energy in the form of ATP. The compound is also involved in the synthesis of certain neurotransmitters and has been studied for its potential role in various metabolic disorders and diseases.

3997-91-9

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3997-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3997-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,9 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3997-91:
(6*3)+(5*9)+(4*9)+(3*7)+(2*9)+(1*1)=139
139 % 10 = 9
So 3997-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO4/c1-3(7)5(10)6-2-4(8)9/h2H2,1H3,(H,6,10)(H,8,9)

3997-91-9SDS

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 2-(2-oxopropanoylamino)acetic acid

1.2 Other means of identification

Product number -
Other names pyruvoylglycine

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:3997-91-9 SDS

3997-91-9Relevant academic research and scientific papers

Highly Lipophilic Benzoxazoles with Potential Antibacterial Activity

Vinsova, Jarmila,Horak, Vaclav,Buchta, Vladimir,Kaustova, Jarmila

, p. 760 - 770 (2007/10/03)

A series of lipophilic 2-substituted 5,7-di-tert-butylbenzoxazoles was prepared in average yields by the reaction of 3,5-di-tert-butyl-1,2-benzoquinone with amino acids and dipeptides bearing N-terminal glycine. Dipeptides having other N-terminal amino acids undergo oxidative deamination. 5,7-Di-tert-butylbenzoxazoles have shown activity against Mycobacterium tuberculosis and some nontuberculous strains where isoniazid has been inactive. Antifungal activity was mediocre.

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