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D-Alaninamide, N-benzoylglycyl-L-prolyl-D-leucyl-N-hydroxyis a peptide derivative that acts as an inhibitor of the enzyme dipeptidyl peptidase-4 (DPP-4), which plays a role in regulating blood sugar levels. It is known for its potential therapeutic use in the treatment of type 2 diabetes and other metabolic disorders.
Used in Pharmaceutical Industry:
D-Alaninamide, N-benzoylglycyl-L-prolyl-D-leucyl-N-hydroxyis used as a DPP-4 inhibitor for improving glucose metabolism and insulin sensitivity in the body. Its structure and properties make it a promising candidate for the development of new medications for diabetes and related conditions.

124169-03-5

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124169-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124169-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124169-03:
(8*1)+(7*2)+(6*4)+(5*1)+(4*6)+(3*9)+(2*0)+(1*3)=105
105 % 10 = 5
So 124169-03-5 is a valid CAS Registry Number.

124169-03-5SDS

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 Bz-Gly-Pro-D-Leu-D-Ala-NHOH

1.2 Other means of identification

Product number -
Other names (S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carboxylic acid [(R)-1-((R)-1-hydroxycarbamoyl-ethylcarbamoyl)-3-methyl-butyl]-amide

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:124169-03-5 SDS

124169-03-5Downstream Products

124169-03-5Relevant academic research and scientific papers

Vertebrate collagenase inhibitor. II. Tetrapeptidyl hydroxamic acids

Odake,Okayama,Obata,Morikawa,Hattori,Hori,Nagai

, p. 1489 - 1494 (2007/10/02)

To develop a potent and specific collagenase inhibitor, a series of tetrapeptidyl hydroxamic acids were synthesized, based on the previous findings with tripeptidyl derivatives (Chem. Pharm. Bull., 38, 1007-1011, 1990). Among the series of tetrapeptidyl d

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