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tert-butyl 4-(2-chloro-4-fluorophenyl)-5-cyano-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1226774-10-2

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1226774-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1226774-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,7,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1226774-10:
(9*1)+(8*2)+(7*2)+(6*6)+(5*7)+(4*7)+(3*4)+(2*1)+(1*0)=152
152 % 10 = 2
So 1226774-10-2 is a valid CAS Registry Number.

1226774-10-2Relevant academic research and scientific papers

Stereochemical requirements for the mineralocorticoid receptor antagonist activity of dihydropyridines

Arhancet, Graciela B.,Woodard, Scott S.,Dietz, Jessica D.,Garland, Danny J.,Wagner, Grace M.,Iyanar, Kaliappan,Collins, Joe T.,Blinn, James R.,Numann, Randal E.,Hu, Xiao,Huang, Horng-Chih

experimental part, p. 4300 - 4304 (2010/08/22)

A number of known 1,4-dihydropyridine CCBs were identified as having comparable potency to the steroidal MR antagonist eplerenone. Chiral resolution of mebudipine revealed that MR and CCB activity reside in opposite enantiomers. Small molecule X-ray crystal structures showed that the C4 stereochemistry of optimized selective MR analogues, e.g. 5, is consistent with MR-active mebudipine. Molecular modeling supports a binding pose consistent with that previously proposed for DHP diesters.

Discovery of novel cyanodihydropyridines as potent mineralocorticoid receptor antagonists

Arhancet, Graciela B.,Woodard, Scott S.,Iyanar, Kaliappan,Case, Brenda L.,Woerndle, Rhonda,Dietz, Jessica D.,Garland, Danny J.,Collins, Joe T.,Payne, Maria A.,Blinn, James R.,Pomposiello, Silvia I.,Hu, Xiao,Heron, Marcia I.,Huang, Horng-Chih,Lee, Len F.

experimental part, p. 5970 - 5978 (2010/11/02)

A new 1,4-dihydropyridine 5a, containing a cyano group at the C3 position, was recently reported to possess excellent mineralocorticoid receptor (MR) antagonist in vitro potency and no calcium channel-blocker (CCB) activity. In the present study, we report the structure-activity relationships of this novel series of cyano ester dihydropyridines that resulted in R6 substituted analogues with improved metabolic stability while maintaining excellent MR antagonist activity and selectivity against other nuclear receptors. Further structure optimization with the introduction of five-membered ring heterocycles at R6 resulted in compounds with excellent MR antagonist potency and a suitable pharmacokinetic profile. In vivo studies of a promising tool compound in the Dahl salt-sensitive rat model of hypertension showed similar blood pressure (BP) reduction as the steroidal MR antagonist eplerenone, providing proof-of-concept (POC) for a nonsteroidal, orally efficacious MR antagonist.

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