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5-fluoro-1-(4-methoxybenzyl)-1,3-dihydro-2H-indol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

769965-93-7

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769965-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 769965-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,9,6 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 769965-93:
(8*7)+(7*6)+(6*9)+(5*9)+(4*6)+(3*5)+(2*9)+(1*3)=257
257 % 10 = 7
So 769965-93-7 is a valid CAS Registry Number.

769965-93-7Relevant academic research and scientific papers

Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors

Tully, David C.,Liu, Hong,Chatterjee, Arnab K.,Alper, Phil B.,Williams, Jennifer A.,Roberts, Michael J.,Mutnick, Daniel,Woodmansee, David H.,Hollenbeck, Thomas,Gordon, Perry,Chang, Jonathan,Tuntland, Tove,Tumanut, Christine,Li, Jun,Harris, Jennifer L.,Karanewsky, Donald S.

, p. 5107 - 5111 (2007/10/03)

We report a novel series of noncovalent inhibitors of cathepsin S. The synthesis of the peptidomimetic scaffold is described and structure-activity relationships of P3, P1, and P1′ subunits are discussed. Lead optimization to a non-peptidic scaffold has r

INHIBITORS OF CATHEPSIN S

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Page/Page column 44, (2008/06/13)

The present invention provides compounds, compositions and methods for the selective inhibition of cathepsin S. In a preferred aspect, cathepsin S is selectively inhibited in the presence of at least one other cathepsin isozyme. The present invention also provides methods for treating a disease state in a subject by selectively inhibiting cathepsin S.

INHIBITORS OF CATHEPSIN S

-

Page/Page column 36, (2008/06/13)

The present invention provides compounds, compositions and methods for the selective inhibition of cathepsin S. In a preferred aspect, cathepsin S is selectively inhibited in the presence of at least one other cathepsin isozyme. The present invention also provides methods for treating a disease state in a subject by selectively inhibiting cathepsin S.

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