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438218-14-5

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438218-14-5 Usage

General Description

The chemical 7-(difluoromethyl)-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid is a pyrazolopyrimidine derivative with a carboxylic acid functional group. It has the molecular formula C8H6F2N4O2 and a molecular weight of 238.16 g/mol. 7-(difluoromethyl)-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid(SALTDATA: FREE) is used in pharmaceutical research and development as a building block for the synthesis of potential drug candidates. Its structure and properties make it a valuable tool for medicinal chemists and drug discovery researchers in the development of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 438218-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,2,1 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 438218-14:
(8*4)+(7*3)+(6*8)+(5*2)+(4*1)+(3*8)+(2*1)+(1*4)=145
145 % 10 = 5
So 438218-14-5 is a valid CAS Registry Number.

438218-14-5Relevant articles and documents

Discovery, structure - Activity relationship, and biological evaluation of noninhibitory small molecule chaperones of glucocerebrosidase

Patnaik, Samarjit,Zheng, Wei,Choi, Jae H.,Motabar, Omid,Southall, Noel,Westbroek, Wendy,Lea, Wendy A.,Velayati, Arash,Goldin, Ehud,Sidransky, Ellen,Leister, William,Marugan, Juan J.

, p. 5734 - 5748 (2012/08/07)

A major challenge in the field of Gaucher disease has been the development of new therapeutic strategies including molecular chaperones. All previously described chaperones of glucocerebrosidase are enzyme inhibitors, which complicates their clinical development because their chaperone activity must be balanced against the functional inhibition of the enzyme. Using a novel high throughput screening methodology, we identified a chemical series that does not inhibit the enzyme but can still facilitate its translocation to the lysosome as measured by immunostaining of glucocerebrosidase in patient fibroblasts. These compounds provide the basis for the development of a novel approach toward small molecule treatment for patients with Gaucher disease. This article not subject to U.S. Copyright. Published 2012 by the American Chemical Society.

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