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866022-28-8

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866022-28-8 Usage

Uses

Bischloroanthrabenzoxocinone ((-)BABX) is a selective inhibitor of Type II fatty acid synthesis (FASII). BABX showed IC50 values of 11.4 and 35.3 μg/ml in the S. aureus and E. coli FASII assays, respectively, with comparable antibacterial activities. Type II fatty acid synthesis (FASII) is essential to bacterial cell viability and is a promising target for the development of novel antibiotics. More recently, BABX has been shown to inhibit agonist binding to Liver X receptors (LXR). The receptors regulate the expression of the ABCA1 gene, which mediates the efflux of cholesterol from cells.

Check Digit Verification of cas no

The CAS Registry Mumber 866022-28-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,0,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 866022-28:
(8*8)+(7*6)+(6*6)+(5*0)+(4*2)+(3*2)+(2*2)+(1*8)=168
168 % 10 = 8
So 866022-28-8 is a valid CAS Registry Number.

866022-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name CTK5F7002

1.2 Other means of identification

Product number -
Other names BISCHLOROANTHRABENZOXOCINONE

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:866022-28-8 SDS

866022-28-8Upstream product

866022-28-8Downstream Products

866022-28-8Relevant articles and documents

Aromatic polyketone compounds, and synthesis method and application thereof

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Paragraph 0238; 0346-0355, (2021/07/01)

The invention discloses a synthesis method of aromatic polyketone products and analogues thereof. Intermolecular Diels-Alder reaction is performed on a formula 1a and a formula 2a to prepare a formula 3a, and a formula 4a is protected by using an ether ad

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