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924644-05-3

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924644-05-3 Usage

Chemical Class

Belongs to the class of piperazinecarboxylic acids and esters.

Type of Compound

Phenylmethyl ester of 4-(2-amino-4-pyrimidinyl) piperazinecarboxylic acid.

Medical Use

Commonly used in veterinary medicine to treat pain and inflammation in dogs.

Mechanism of Action

Inhibits the action of cyclooxygenase (COX) enzymes, which are responsible for the production of inflammatory prostaglandins.

COX Inhibition Profile

Selective COX-2 inhibitor, targeting primarily the COX-2 enzyme involved in the inflammatory response.

Gastrointestinal Health

Spares the COX-1 enzyme, which is important for maintaining the health of the gastrointestinal tract.

Check Digit Verification of cas no

The CAS Registry Mumber 924644-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,6,4 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 924644-05:
(8*9)+(7*2)+(6*4)+(5*6)+(4*4)+(3*4)+(2*0)+(1*5)=173
173 % 10 = 3
So 924644-05-3 is a valid CAS Registry Number.

924644-05-3Downstream Products

924644-05-3Relevant articles and documents

Inhibitors of P2X3

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Page/Page column 10, (2008/06/13)

Compounds of formula 1 are modulators of P2X3 useful for the treatment of pain and genito-urinary, gastrointestinal, and respiratory disorders: wherein R1 is —C(═S)CH3, pyridyl, pyrimidinyl, pyrazinyl, thiazolyl, furyl, furylcarbonyl, acetyl, or carbamoyl; R2a and R2b are independently H, methyl, or ethyl; R3 is H or methyl; Y is a bond, —(CR4R5)n— or —CR4═CR5—; wherein R4 and R5 are each independently H or methyl and n is 1 or 2; X is N or CH; A is phenyl, 5-membered heterocyclyl, or 6-membered heterocyclyl; R6, R7 and R8 are each independently H, halo, lower alkyl, cycloalkyl, alkylthio, alkylthio-lower alkyl, alkylsulfonyl-lower alkyl, di(lower alkyl)amino-lower alkyl, morpholinyl-lower alkyl, 4-methyl-piperazinyl-methyl, trifluoromethyl, pyridyl, tetrazolyl, thiophenyl, phenyl, biphenyl, or benzyl (where thiophenyl, phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoromethyl, lower alkoxy or lower alkylthio) or R6 and R7 together form a 5-membered or 6-membered carbocyclic or heterocyclic ring substituted with 0-3 substituents selected from the group consisting of lower alkyl, lower alkoxy, oxo, halo, thiophenyl-lower alkyl, phenyl, benzyl (where phenyl and benzyl are substituted with 0-3 lower alkyl, halo, sulfonamido, trifluoro-methyl, lower alkoxy, lower alkylthio, amino-lower alkyl, lower alkylamino-lower alkyl, or di(lower alkyl)amino-lower alkyl); and pharmaceutically acceptable salts thereof; wherein when R1 is pyrimidin-2-yl, X is N, Y is a bond and A is oxazol-5-yl the carbon atom at position 4 in said oxazol-5-yl is not substituted by propyl when the carbon atom at position 2 in said oxazol-5-yl is substituted by substituted phenyl and the carbon atom at position 4 in said oxazol-5-yl is not substituted by phenyl when the carbon atom at position 2 is substituted by unsubstituted or substituted phenyl.

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