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Carbamic acid, [5-[[[3-[[[(1R)-1-(4-fluorophenyl)ethyl]amino]carbonyl]-5-hydroxyphenoxy] acetyl]amino]pentyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

787620-91-1

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787620-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 787620-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,7,6,2 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 787620-91:
(8*7)+(7*8)+(6*7)+(5*6)+(4*2)+(3*0)+(2*9)+(1*1)=211
211 % 10 = 1
So 787620-91-1 is a valid CAS Registry Number.

787620-91-1Downstream Products

787620-91-1Relevant academic research and scientific papers

PHENYL CARBOXAMIDE COMPOUNDS USEFUL AS BETA-SECRETASE INHIBITORS FOR THE TREATMENT OF ALZHEIMER'S DISEASE

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, (2010/02/14)

The present invention is directed to phenyl carboxamide compounds which are inhibitors of the beta-secretase enzyme and that are useful in the treatment of diseases in which the beta-secretase enzyme is involved, such as Alzheimer's disease. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the treatment of such diseases in which the beta-secretase enzyme is involved.

Identification of a small molecule nonpeptide active site β-secretase inhibitor that displays a nontraditional binding mode for aspartyl proteases

Coburn, Craig A.,Stachel, Shawn J.,Li, Yue-Ming,Rush, Diane M.,Steele, Thomas G.,Chen-Dodson, Elizabeth,Holloway, M. Katharine,Xu, Min,Huang, Qian,Lai, Ming-Tain,DiMuzio, Julian,Crouthamel, Ming-Chih,Shi, Xiao-Ping,Sardana, Vinod,Chen, Zhongguo,Munshi, Sanjeev,Kuo, Lawrence,Makara, Gergely M.,Annis, D. Allen,Tadikonda, Praveen K.,Nash, Huw M.,Vacca, Joseph P.,Wang, Tong

, p. 6117 - 6119 (2007/10/03)

A small molecule nonpeptide inhibitor of β-secretase has been developed, and its binding has been defined through crystallographic determination of the enzyme-inhibitor complex. The molecule is shown to bind to the catalytic aspartate residues in an unprecedented manner in the field of aspartyl protease inhibition. Additionally, the complex reveals a heretofore unknown 83 subpocket that is created by the inhibitor. This structure has served an important role in the design of newer β-secretase inhibitors.

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