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NSC45719 is a chemical compound identified as a potent and selective inhibitor of the protein kinase PDK1 (3-phosphoinositide-dependent protein kinase-1). It plays a critical role in cell growth, proliferation, and survival, making it an attractive target for anti-cancer therapies. Research has shown that NSC45719 effectively inhibits PDK1 activity, leading to the suppression of tumor growth in several cancer cell lines. It also demonstrates promising potential for the treatment of other diseases characterized by dysregulated PDK1 activity, such as diabetes and cardiovascular disorders. Furthermore, studies have indicated that NSC45719 may act through a unique mechanism, making it a valuable tool for further investigation into PDK1 signaling pathways and the development of targeted therapeutics.

6632-63-9

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6632-63-9 Usage

Uses

Used in Pharmaceutical Industry:
NSC45719 is used as an anti-cancer agent for its ability to effectively inhibit the activity of PDK1, leading to the suppression of tumor growth in various cancer cell lines.
Used in Research and Development:
NSC45719 is used as a valuable tool for further investigation into PDK1 signaling pathways, aiding in the development of targeted therapeutics for diseases characterized by dysregulated PDK1 activity.
Used in Treatment of Diabetes and Cardiovascular Disorders:
NSC45719 is used as a potential treatment for diseases such as diabetes and cardiovascular disorders, due to its promising potential in addressing dysregulated PDK1 activity in these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6632-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6632-63:
(6*6)+(5*6)+(4*3)+(3*2)+(2*6)+(1*3)=99
99 % 10 = 9
So 6632-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClN2OS/c1-10-5-7-3(6)2-4(9)8-5/h2H,1H3,(H,7,8,9)

6632-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-methylsulfanyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 4-chloro-6-hydroxy-2-methylthiopyrimidine

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:6632-63-9 SDS

6632-63-9Relevant academic research and scientific papers

HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF

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Page/Page column 173, (2022/02/22)

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; (I) wherein R1 R2, R4 and X1 are defeined herein, a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

SHP2 PHOSPHATASE INHIBITORS AND METHODS OF USE THEREOF

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Paragraph 0368; 0370, (2019/09/12)

The present disclosure relates to novel compounds and pharmaceutical compositions thereof, and methods for inhibiting the activity of SHP2 phosphatase with the compounds and compositions of the disclosure. The present disclosure further relates to, but is not limited to, methods for treating disorders associated with SHP2 deregulation with the compounds and compositions of the disclosure.

PYRIMIDINE DERIVATIVES FOR THE TREATMENT OP GABA B MEDIATED NERVOUS SYSTEM DISORDERS

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Page/Page column 22, (2010/11/25)

The invention relates to novel heterocyclic compounds of the formula (I) in free base form or in acid addition salt form, in which R1, R2, R3, R4 and A are as defined in the specification, to their preparation, to their use as medicaments for the treatment of certain nervous system disorders and to medicaments comprising them.

Identification and Synthesis of a Unique Disulfide Dimeric Metabolite of Primisulfuron-methyl in the Mouse

Capps, Thomas M.,Heard, Nina E.,Simmons, Dana P.,Connor, Connie L.

, p. 2411 - 2415 (2007/10/02)

The major metabolic pathway for primisulfuron-methyl in animals involves hydroxylation of the pyrimidine ring followed by conjugation.This investigation found a unique metabolite in mice fed at high feeding levels (>5000 ppm) of the compound.The unique metabolite is identified as a disulfide dimer of the parent compound, and its synthesis is reported.

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