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dibenzyl 1-((4-(6-(4-chlorophenyl)-4-oxothieno[3,2-d]-pyrimidin-3(4H)-yl)-2-methoxyphenoxy)methyl)-3,3-difluorocyclobutyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1197420-29-3

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1197420-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197420-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,4,2 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1197420-29:
(9*1)+(8*1)+(7*9)+(6*7)+(5*4)+(4*2)+(3*0)+(2*2)+(1*9)=163
163 % 10 = 3
So 1197420-29-3 is a valid CAS Registry Number.

1197420-29-3Relevant academic research and scientific papers

Synthesis and Antiobesity Properties of 6-(4-Chlorophenyl)-3-(4-((3,3-difluoro-1-hydroxycyclobutyl)methoxy)-3-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one (BMS-814580): A Highly Efficacious Melanin Concentrating Hormone Receptor 1 (MCHR1) Inhibitor

Ahmad, Saleem,Washburn, William N.,Hernandez, Andres S.,Bisaha, Sharon,Ngu, Khehyong,Wang, Wei,Pelleymounter, Mary Ann,Longhi, Daniel,Flynn, Neil,Azzara, Anthony V.,Rohrbach, Kenneth,Devenny, James,Rooney, Suzanne,Thomas, Michael,Glick, Susan,Godonis, Helen,Harvey, Susan,Zhang, Hongwei,Gemzik, Brian,Janovitz, Evan B.,Huang, Christine,Zhang, Lisa,Robl, Jeffrey A.,Murphy, Brian J.

, p. 8848 - 8858 (2016/10/22)

The potent MCHR1 in vitro and in vivo antagonist activity of a series of cyclic tertiary alcohols derived from compound 2b is described. Subsequent pharmacokinetic and pharmacodynamic studies identified BMS-814580 (compound 10) as a highly efficacious antiobesity agent with a relatively clean in vitro and in vivo safety profile.

HYDROXY SUBSTITUTED THIENO PYRIMIDINONES AS MELANIN CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS

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Page/Page column 24, (2009/12/23)

The present invention provides compounds having the following Formula IA and IB, which are useful as MCHR1 antagonists, and includes prodrugs and pharmaceutically acceptable salts thereof:

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