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(R)-5-hydroxy-2-aminovaleric acid, also known as (R)-HAVA, is a chemical compound that belongs to the family of hydroxy amino acids. It is a derivative of L-lysine and is involved in the biosynthesis of the neurotransmitter gamma-aminobutyric acid (GABA). (R)-HAVA has been found to have potential therapeutic applications in the treatment of neurological disorders, as it may act as a GABA analogue and modulate GABAergic neurotransmission. Additionally, (R)-HAVA has been studied for its role in antifungal and antibacterial activities, making it a candidate for the development of new antimicrobial agents. Overall, (R)-5-hydroxy-2-aminovaleric acid is a multifaceted compound with promising pharmacological properties that warrant further investigation.

6152-90-5

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6152-90-5 Usage

Uses

Used in Pharmaceutical Industry:
(R)-HAVA is used as a therapeutic agent for neurological disorders due to its potential as a GABA analogue and its ability to modulate GABAergic neurotransmission.
Used in Antimicrobial Applications:
(R)-HAVA is used as an antimicrobial agent for its antifungal and antibacterial activities, making it a candidate for the development of new antimicrobial agents.
Used in Research and Development:
(R)-HAVA is used as a compound in the research and development of new pharmaceuticals and treatments, particularly in the areas of neurological disorders and infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 6152-90-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6152-90:
(6*6)+(5*1)+(4*5)+(3*2)+(2*9)+(1*0)=85
85 % 10 = 5
So 6152-90-5 is a valid CAS Registry Number.

6152-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-5-hydroxy-2-aminovaleric acid

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-D-norvalin

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:6152-90-5 SDS

6152-90-5Downstream Products

6152-90-5Relevant academic research and scientific papers

Micropeptins from the freshwater cyanobacterium Microcystis aeruginosa (NIES-100)

Kisugi, Takaya,Okino, Tatsufumi

, p. 777 - 781 (2009)

Micropeptins C (1), D (2), E (3), and F (4) have been isolated from the freshwater cyanobacterium Microcystis aeruginosa (NIES-100). The structures were elucidated by analyses of MS, NMR spectra, and chemical degradation. Micropeptins C, D, E, and F inhib

Biosynthesis of 4-methylproline in cyanobacteria: Cloning of nosE and nosF genes and biochemical characterization of the encoded dehydrogenase and reductase activities

Luesch, Hendrik,Hoffmann, Dietmar,Hevel, Joan M.,Becker, Julia E.,Golakoti, Trimurtulu,Moore, Richard E.

, p. 83 - 91 (2007/10/03)

The biosynthesis of the unusual amino acid 4-methylproline in the Nostoc genus of cyanobacteria was investigated on the genetic and enzymatic level. Two genes involved in the biosynthesis were cloned and the corresponding enzymes, a zinc-dependent long-chain dehydrogenase and a Δ1-pyrroline-5-carboxylic acid (P5C) reductase homologue, were overexpressed in Escherichia coli and biochemically characterized. Putative substrates were synthesized to test enzyme substrate specificities, and deuterium labeling studies were carried out to reveal the stereospecificities of the enzymatic reactions with respect to the substrates as well as to the coenzymes.

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