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138079-74-0

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138079-74-0 Usage

General Description

N-Benxoyl-D-Alanylthioglycolic Acid is a chemical compound that is primarily known for its potential uses in medicinal and biochemical research. It is a peptidyl thiol ester compound that has been studied for its potential to react with certain enzymes in the body. N-BENZOYL-D-ALANYLTHIOGLYCOLIC ACID has been examined for potential in vitro interactions with enzymes such as leucine aminopeptidase, a protein-coding gene that may affect several biological processes including protein metabolic process, viral process, and proteolysis. However, more extensive research is required to understand the full biochemical nature and potential applications of N-Benxoyl-D-Alanylthioglycolic Acid in medicine and molecular biology. Currently, it is generally used as a research tool in laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 138079-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,0,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138079-74:
(8*1)+(7*3)+(6*8)+(5*0)+(4*7)+(3*9)+(2*7)+(1*4)=150
150 % 10 = 0
So 138079-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO4S/c1-8(12(17)18-7-10(14)15)13-11(16)9-5-3-2-4-6-9/h2-6,8H,7H2,1H3,(H,13,16)(H,14,15)/p-1/t8-/m1/s1

138079-74-0Downstream Products

138079-74-0Relevant articles and documents

Synthesis of an enantiopure thioester as key substrate for screening the sensitivity of penicillin binding proteins to inhibitors

Simon, Justine F.,Bouillez, André,Frère, Jean-Marie,Luxen, André,Zervosen, Astrid

, p. 22 - 31 (2016/10/31)

The synthesis of the enantiopure thioester (R)-2-(2-benzamidopropanoylthio)acetic acid was developed. After the exploration of several activation methods, reaction conditions were found for the formation of the thioester bond in the presence of propylphosphonic anhydride with high enantioselectivity (ee > 99%). The thioester activity of Penicillin Binding Proteins is helpful in research programs looking for new lead structures to overcome the problem of bacterial resistance.

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