209959-68-2 Usage
Uses
Used in Pharmaceutical Research:
(2-chloro-4-nitrophenyl)-1-pyrrolidinylMethanone is used as a research compound for studying the endocannabinoid system and its role in various physiological processes. Its ability to inhibit the enzyme FAAH makes it a valuable tool in understanding the mechanisms of pain and inflammation regulation.
Used in Drug Development:
As an FAAH inhibitor, (2-chloro-4-nitrophenyl)-1-pyrrolidinylMethanone is used in the development of potential therapeutic agents for the treatment of pain and inflammation-related disorders. Its modulation of the endocannabinoid system offers a novel approach to managing these conditions and could lead to the discovery of new medications with improved efficacy and safety profiles.
Used in Medical Research:
(2-chloro-4-nitrophenyl)-1-pyrrolidinylMethanone is employed in medical research to explore its potential therapeutic applications beyond pain and inflammation. Its effects on the endocannabinoid system suggest that it may have utility in treating a range of other conditions, and ongoing research aims to uncover these possibilities and advance our understanding of its clinical potential.
Check Digit Verification of cas no
The CAS Registry Mumber 209959-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,9,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 209959-68:
(8*2)+(7*0)+(6*9)+(5*9)+(4*5)+(3*9)+(2*6)+(1*8)=182
182 % 10 = 2
So 209959-68-2 is a valid CAS Registry Number.
209959-68-2Relevant academic research and scientific papers
NITROGEN CONTAINING HETEROAROMATICS AS FACTOR Xa INHIBITORS
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Page/Page column 73, (2009/10/01)
The present application describes nitrogen containing heteroaromatics and derivatives thereof of formula (I) or pharmaceutically acceptable salt or prodrug forms thereof, wherein J is N or NH and D may be C(=NH)NH2, which are useful as inhibitors of factor Xa.
SUBSTITUTED THIOPHEN-CARBOXYLIC ACID AMIDES, THE PRODUCTION AND THE USE THEREOF IN THE FORM OF A DRUG
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Page/Page column 130, (2010/02/14)
The invention relates to novel substituted thiophen-2-carboxylic acid amides of general formula (I), wherein A and R1 to R8 are defined as specified in the claim 1, the tautomers, enantiomers, diastereomers, mixtures and salts thereof, in particular the salts thereof which are physiologically compatible with inorganic or organic acids or bases and exhibit interesting properties.
Carboxylic acid amides having antithrombotic activity
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, (2008/06/13)
Compounds with antithrombotic activity and factor Xa-inhibiting activity of the general formula: Exemplary are: (1) (L)-2-(5-carbamimidoyl-2-hydroxy-phenyl)-N-[3-methyl-4-(2-aminocarbonyl-pyrrolidin-1-yl-carbonyl)-phenyl]-acetamide, (2) 2-(5-carbamimidoyl
