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L-Kynurenine sulfate is a chemical compound derived from the amino acid tryptophan, playing a crucial role in the kynurenine pathway of tryptophan metabolism. It has been studied for its potential therapeutic applications, particularly in the treatment of neurodegenerative diseases and psychiatric disorders, as well as its involvement in immune regulation and inflammation. Ongoing research continues to explore its health benefits and mechanisms of action.

13535-93-8

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13535-93-8 Usage

Uses

Used in Pharmaceutical Industry:
L-Kynurenine sulfate is used as a therapeutic agent for the treatment of neurodegenerative diseases and psychiatric disorders due to its potential neuroprotective and modulatory effects on neurotransmission.
Used in Immunology Research:
L-Kynurenine sulfate is used as a research tool to study its role in immune regulation and inflammation, providing insights into the development of novel immunomodulatory therapies.
Used in Metabolic Studies:
L-Kynurenine sulfate is utilized in metabolic research to understand its role in the kynurenine pathway and its implications in various physiological and pathological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 13535-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13535-93:
(7*1)+(6*3)+(5*5)+(4*3)+(3*5)+(2*9)+(1*3)=98
98 % 10 = 8
So 13535-93-8 is a valid CAS Registry Number.

13535-93-8SDS

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 2-amino-4-(2-aminophenyl)-4-oxobutanoic acid,sulfuric acid

1.2 Other means of identification

Product number -
Other names -

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:13535-93-8 SDS

13535-93-8Downstream Products

13535-93-8Related news

Neuroprotective effect of L-KYNURENINE SULFATE (cas 13535-93-8) administered before focal cerebral ischemia in mice and global cerebral ischemia in gerbils08/12/2019

Excessive stimulation of N-methyl-D-aspartate (NMDA) receptors during ischemia contributes to apoptotic and excitotoxic nerve cell death. Kynurenic acid is a selective antagonist at the glycine co-agonist site of the NMDA receptor complex at low concentration, and it is a broad-spectrum excitato...detailed

Post-ischemic treatment with L-KYNURENINE SULFATE (cas 13535-93-8) exacerbates neuronal damage after transient middle cerebral artery occlusion08/11/2019

Since brain ischemia is one of the leading causes of adult disability and death, neuroprotection of the ischemic brain is of particular importance. Acute neuroprotective strategies usually have the aim of suppressing glutamate excitotoxicity and an excessive N-methyl-d-aspartate (NMDA) receptor ...detailed

13535-93-8Relevant academic research and scientific papers

A concise preparation of the non-proteinogenic amino acid l-kynurenine

Kleijn, Laurens H.J.,Müskens, Frederike M.,Oppedijk, Sabine F.,De Bruin, Gerjan,Martin, Nathaniel I.

supporting information, p. 6430 - 6432 (2013/01/15)

A concise and practical preparation of the non-proteinogenic amino acid l-kynurenine is reported. The synthetic approach is scalable and provides ready access to this valuable amino acid in either l- or d-stereochemistry starting from l- or d-tryptophan, respectively. In the optimized procedure, two discreet oxidation steps are applied sequentially to convert the tryptophan indole ring into the keto-aniline moiety contained within the kynurenine side chain.

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