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1-PROPIONYL-2,3-DIHYDRO-1H-INDOLE-5-SULFONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868963-99-9

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868963-99-9 Usage

Type of compound

sulfonyl chloride derivative

Parent compound

1-propionyl-2,3-dihydro-1H-indole-5-sulfonyl

Usage

reagent in chemical synthesis and pharmaceutical research

Application

preparation of indole-based pharmaceuticals, agrochemicals, and biologically active molecules

Reactive group

sulfonyl chloride functional group

Purpose

introduction of 1-propionyl-2,3-dihydro-1H-indole-5-sulfonyl moiety into organic molecules

Importance

valuable tool for drug discovery and development

Structural feature

indole ring

Potential activities

pharmaceutical and biological activities

Industry relevance

versatile and important intermediate in the chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 868963-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,9,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 868963-99:
(8*8)+(7*6)+(6*8)+(5*9)+(4*6)+(3*3)+(2*9)+(1*9)=259
259 % 10 = 9
So 868963-99-9 is a valid CAS Registry Number.

868963-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propanoyl-2,3-dihydroindole-5-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 1-Propionyl-2,3-dihydro-1H-indole-5-sulfonyl chloride

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:868963-99-9 SDS

868963-99-9Relevant academic research and scientific papers

Identification of inhibitors of NOD1-induced nuclear factor-κB activation

Khan, Pasha M.,Correa, Ricardo G.,Divlianska, Daniela B.,Peddibhotla, Satyamaheshwar,Sessions, E. Hampton,Magnuson, Gavin,Brown, Brock,Suyama, Eigo,Yuan, Hongbin,Mangravita-Novo, Arianna,Vicchiarelli, Michael,Su, Ying,Vasile, Stefan,Smith, Layton H.,Diaz, Paul W.,Reed, John C.,Roth, Gregory P.

experimental part, p. 780 - 785 (2011/12/02)

NOD1 (nucleotide-binding oligomerization domain 1) protein is a member of the NLR (NACHT and leucine rich repeat domain containing proteins) protein family, which plays a key role in innate immunity as a sensor of specific microbial components derived from bacterial peptidoglycans and induction of inflammatory responses. Mutations in NOD proteins have been associated with various inflammatory diseases that affect NF-κB (nuclear factor κB) activity, a major signaling pathway involved in apoptosis, inflammation, and immune response. A luciferase-based reporter gene assay was utilized in a high-throughput screening program conducted under the NIH-sponsored Molecular Libraries Probe Production Center Network program to identify the active scaffolds. Herein, we report the chemical synthesis, structure-activity relationship studies, downstream counterscreens, secondary assay data, and pharmacological profiling of the 2-aminobenzimidazole lead (compound 1c, ML130) as a potent and selective inhibitor of NOD1-induced NF-κB activation.

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