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288862-58-8

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288862-58-8 Usage

Structure

Contains an oxazolo-pyridine ring system

Type

Synthetic chemical compound

Applications

Potential use in pharmaceutical research and drug development

Pharmacological activities

Anti-inflammatory, anti-cancer, and antimicrobial properties

Status

Promising candidate for the development of new drugs

Importance

Unique chemical structure and potential biological activities make it an interesting compound for further exploration in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 288862-58-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,8,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 288862-58:
(8*2)+(7*8)+(6*8)+(5*8)+(4*6)+(3*2)+(2*5)+(1*8)=208
208 % 10 = 8
So 288862-58-8 is a valid CAS Registry Number.

288862-58-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-([1,3]oxazolo[4,5-b]pyridin-2-yl)octadec-9-en-1-one

1.2 Other means of identification

Product number -
Other names oleoyl oxazolopyridine

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:288862-58-8 SDS

288862-58-8Upstream product

288862-58-8Downstream Products

288862-58-8Relevant articles and documents

Inhibitors of fatty acid amide hydrolase

-

, (2008/06/13)

Potent inhibitors of fatty acid amide hydrolase (FAAH) are constructed having Ki's below 200 pM and activities 102-103times more potent than the corresponding trifluoromethyl ketones. The potent inhibitors combine several features, viz.: 1.) an α-keto heterocylic head group; 2.) a hydrocarbon linkage unit employing an optimal C12-C8 chain length; and 3.) a phenyl or other π-unsaturation corresponding to the arachidonyl Δ8.9/Δ11.12and/or oleyl Δ9.10positions. A preferred α-keto heterocylic head group is α-keto N4 oxazolopyridine, with incorporation of a second weakly basic nitrogen. Fatty acid amide hydrolase is an enzyme responsible for the degradation of oleamide (an endogenous sleep-inducing lipid) and anandamide (an endogenous ligand for cannabinoid receptors).

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