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N-[4-(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl)phenyl]acetamide is a complex organic compound with a unique molecular structure. It is characterized by its allyl and butyl substituents on the purine core, which is connected to a phenyl group through an amide linkage. This molecule exhibits a diverse range of biological activities, making it a promising candidate for various pharmaceutical applications.

628279-02-7

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628279-02-7 Usage

Uses

Used in Pharmaceutical Industry:
N-[4-(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl)phenyl]acetamide is used as a key intermediate for the preparation of amide-substituted xanthine derivatives. These derivatives act as phosphoenolpyruvate carboxykinase (PEPCK) inhibitors, which play a crucial role in modulating gluconeogenesis. By inhibiting PEPCK, these compounds can help regulate blood glucose levels and are, therefore, valuable in the development of treatments for type 2 diabetes.

Check Digit Verification of cas no

The CAS Registry Mumber 628279-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,2,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 628279-02:
(8*6)+(7*2)+(6*8)+(5*2)+(4*7)+(3*9)+(2*0)+(1*2)=177
177 % 10 = 7
So 628279-02-7 is a valid CAS Registry Number.

628279-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names N-{4-[(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl )methyl]phenyl}acetamide

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:628279-02-7 SDS

628279-02-7Relevant academic research and scientific papers

Modified 3-alkyl-1,8-dibenzylxanthines as GTP-competitive inhibitors of phosphoenolpyruvate carboxykinase

Foley, Louise H.,Wang, Ping,Dunten, Pete,Ramsey, Gwendolyn,Gubler, Mary-Lou,Wertheimer, Stanley J.

, p. 3607 - 3610 (2007/10/03)

The first non-substrate like inhibitors of human cytosolic phosphoenolpyruvate carboxykinase (PEPCK) competitive with GTP are reported. An effort to discover orally active compounds that improve glucose homeostasis in Type 2 diabetics by reversibly inhibi

AMIDE SUBSTITUTED XANTHINE DERIVATIVES WITH GLUCONEOGENESIS MODULATING ACTIVITY

-

, (2012/04/23)

The present invention is a 1,3,8 substituted xanthine derivative of formula (I) or a pharmaceutically acceptable salt thereof, wherein R1, R2 and R3 are as defined in the specification. Compounds of formula (I) and pharmaceutically acceptable salts or prodrugs thereof show activity as modulators of gluconeogenesis.

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