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H-LEU-ASP-OH is a chemical compound composed of the amino acids leucine and aspartic acid, along with a hydroxyl group. Leucine, a branched-chain amino acid, is crucial for protein synthesis and muscle growth, while aspartic acid, a non-essential amino acid, is involved in the urea cycle and citric acid cycle. The hydroxyl group allows for hydrogen bonding and participation in chemical reactions. H-LEU-ASP-OH is frequently utilized in biochemical and pharmaceutical research for peptide synthesis and as a potential therapeutic agent for various medical conditions.

32949-40-9

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32949-40-9 Usage

Uses

Used in Biochemical Research:
H-LEU-ASP-OH is used as a building block for peptide synthesis, enabling the creation of complex protein structures for research purposes.
Used in Pharmaceutical Research:
H-LEU-ASP-OH is used as a potential therapeutic agent for various medical conditions, leveraging its unique combination of amino acids and the hydroxyl group for targeted treatments.
Used in Protein Synthesis:
H-LEU-ASP-OH is used as a component in protein synthesis, contributing to the development and maintenance of muscle mass due to the presence of leucine.
Used in Metabolic Cycles:
H-LEU-ASP-OH is used in the urea cycle and citric acid cycle, with aspartic acid playing a role in these essential metabolic processes.
Used in Hydrogen Bonding and Chemical Reactions:
The hydroxyl group in H-LEU-ASP-OH is used for hydrogen bonding and participating in chemical reactions, which can be vital for the development of new pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 32949-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,4 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32949-40:
(7*3)+(6*2)+(5*9)+(4*4)+(3*9)+(2*4)+(1*0)=129
129 % 10 = 9
So 32949-40-9 is a valid CAS Registry Number.

32949-40-9SDS

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 (2S)-2-[[(2S)-2-amino-4-methylpentanoyl]amino]butanedioic acid

1.2 Other means of identification

Product number -
Other names L-Leu-L-Asp

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:32949-40-9 SDS

32949-40-9Relevant academic research and scientific papers

DPP4 INHIBITOR AND PHARMACEUTICAL APPLICATION THEREOF

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Page/Page column 8-9, (2008/06/13)

The present invention provides a Dpp4 inhibitor which comprises a leucine derivative of the following formula (1) or a methionine derivative of the following formula (2): wherein each R1 and R3 represents a hydrogen atom (H) and an L-amino acid residue; R2 represents a hydroxyl group (OH), alkoxy group having 1 to 6 carbon atoms, amino group (NH2), alkylamino group having 1 to 6 carbon atoms, glycine residue, β-alanine residue, L-amino acid (except for proline, alanine and phenylalanine) residue or L-amino-acid amide (except for proline amide, alanine amide and phenylalanine amide) residue; and R4 represents a hydroxyl group (OH), alkoxy group having 1 to 6 carbon atoms, amino group (NH2), alkylamino group having 1 to 6 carbon atoms, glycine residue, β-alanine residue, L-amino acid (except for proline and alanine) residue or L-amino-acid amide (except for proline amide and alanine amide) residue. These derivatives also act as autophagy regulators.

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