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4-HYDROXYIMINO-PENTANOIC ACID, commonly known as pipecolic acid, is a naturally occurring non-protein amino acid found in plants, animals, and humans. It plays a vital role in the metabolism of lysine and the synthesis of the neurotransmitter gamma-aminobutyric acid (GABA). Pipecolic acid is involved in various biological processes such as immune response modulation, neuroprotection, and oxidative stress reduction. Its potential therapeutic applications include treatments for inflammatory and neurological disorders, as well as a possible role in preventing age-related cognitive decline. Furthermore, pipecolic acid has been studied for its potential as a biomarker in the diagnosis and monitoring of certain health conditions.

6945-36-4

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6945-36-4 Usage

Uses

Used in Pharmaceutical Industry:
4-HYDROXYIMINO-PENTANOIC ACID is used as a therapeutic agent for its potential in treating inflammatory and neurological disorders. Its role in immune response modulation, neuroprotection, and oxidative stress reduction makes it a promising candidate for developing treatments for these conditions.
Used in Neuroprotection:
4-HYDROXYIMINO-PENTANOIC ACID is used as a neuroprotective agent due to its involvement in the synthesis of the neurotransmitter GABA, which plays a crucial role in reducing neuronal excitability and preventing neuronal damage.
Used in Oxidative Stress Reduction:
4-HYDROXYIMINO-PENTANOIC ACID is used as an antioxidant to help reduce oxidative stress, which is implicated in various diseases and aging processes.
Used in Age-Related Cognitive Decline Prevention:
4-HYDROXYIMINO-PENTANOIC ACID is used as a preventive agent for age-related cognitive decline, potentially contributing to maintaining cognitive function and delaying the onset of neurodegenerative diseases.
Used in Diagnostics:
4-HYDROXYIMINO-PENTANOIC ACID is used as a biomarker in the diagnosis and monitoring of certain health conditions, providing valuable information for early detection and treatment planning.

Check Digit Verification of cas no

The CAS Registry Mumber 6945-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6945-36:
(6*6)+(5*9)+(4*4)+(3*5)+(2*3)+(1*6)=124
124 % 10 = 4
So 6945-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO3/c1-4(6-9)2-3-5(7)8/h9H,2-3H2,1H3,(H,7,8)/b6-4-

6945-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-HYDROXYIMINO-PENTANOIC ACID

1.2 Other means of identification

Product number -
Other names 4-Hydroxyimino-valeriansaeure

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:6945-36-4 SDS

6945-36-4Relevant academic research and scientific papers

Acyl acid derivative and preparation method and medical application thereof

-

Paragraph 0443-0446, (2020/07/02)

The invention relates to an acyl acid derivative as well as a preparation method and medical application thereof. Specifically, the invention relates to a compound represented by a general formula (I), a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same, and the invention also relates to a use thereof as an active ingredient in the prevention and/or treatment of muscle atrophy-related diseases, including myogenic muscle atrophy, disuse muscle atrophy, senile muscle atrophy, neurogenic muscle atrophy, and a use in the prevention and/or treatment of obesity, fatty liver, cardiovascular and cerebrovascular diseases, metabolic diseases, and anti-aging, wherein the definition of each group in the general formula (I) is the same as the definition in the specification.

Evaluation of hadacidin analogues

Tibrewal, Nidhi,Elliott, Gregory I.

supporting information; experimental part, p. 517 - 519 (2011/02/25)

Several derivatives of hadacidin have been developed and evaluated for activity against adenylosuccinate synthetase.

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