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Cyclohexanecarboxylic acid, 2-[[(1R)-1-phenylethyl]amino]-, methyl ester, (1S,2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

835926-53-9

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835926-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 835926-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,5,9,2 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 835926-53:
(8*8)+(7*3)+(6*5)+(5*9)+(4*2)+(3*6)+(2*5)+(1*3)=199
199 % 10 = 9
So 835926-53-9 is a valid CAS Registry Number.

835926-53-9Downstream Products

835926-53-9Relevant academic research and scientific papers

Synthesis, preliminary biological evaluation and molecular modeling of some new heterocyclic inhibitors of TACE

Sengupta, Prabal,Puri, Chetan S.,Chokshi, Hemant A.,Sheth, Chetana K.,Midha, Ajay S.,Chitturi, Trinadha Rao,Thennati, Rajamannar,Murumkar, Prashant R.,Yadav, Mange Ram

, p. 5549 - 5555 (2011/12/15)

Central heteroaryl ring analogues belonging to a series of potent hydroxamate TACE inhibitors were synthesized. The TACE inhibitory activities of these compounds were evaluated by in vitro WBA and in silico molecular modeling studies using crystal structure of human TACE. Compound 14 showed very good in vitro inhibition, supported by the in silico docking studies.

5-Amidinobenzo[b]thiophenes as dual inhibitors of factors IXa and Xa

Qiao, Jennifer X.,Cheng, Xuhong,Modi, Dilip P.,Rossi, Karen A.,Luettgen, Joseph M.,Knabb, Robert M.,Jadhav, Prabhakar K.,Wexler, Ruth R.

, p. 29 - 35 (2007/10/03)

Syntheses and SAR studies of 5-amidinobenzo[b]thiophene analogs provided compounds with low submicromolar factor IXa potency and equal or slightly better selectivity relative to factor Xa. Syntheses and SAR studies of 5-amidinobenzo[b]thiophene analogs provided compounds with low submicromolar factor IXa activity and equal or slightly better selectivity relative to factor Xa.

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