886496-96-4 Usage
Chemical structure
Contains a cyclohexane ring with an amino group substituted with a methoxy-phenyl group and a carboxylic acid group.
Potential pharmaceutical applications
Exhibits properties that make it suitable for use in drug development.
Possible biological activities
May possess analgesic, anti-inflammatory, or other biological activities.
Use as a building block
May be used in the synthesis of other pharmacologically active compounds.
Research and development
Its chemical structure and properties make it an interesting target for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 886496-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,4,9 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 886496-96:
(8*8)+(7*8)+(6*6)+(5*4)+(4*9)+(3*6)+(2*9)+(1*6)=254
254 % 10 = 4
So 886496-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO3/c1-18-12-7-5-11(6-8-12)15-14(13(16)17)9-3-2-4-10-14/h5-8,15H,2-4,9-10H2,1H3,(H,16,17)
886496-96-4Relevant academic research and scientific papers
Potent and selective cathepsin K inhibitors
Shinozuka, Tsuyoshi,Shimada, Kousei,Matsui, Satoshi,Yamane, Takahiro,Ama, Mayumi,Fukuda, Takeshi,Taki, Motohiko,Takeda, Yuko,Otsuka, Eri,Yamato, Michiko,Mochizuki, Shin-ichi,Ohhata, Keiko,Naito, Satoru
, p. 6789 - 6806 (2007/10/03)
A novel series of cathepsin K inhibitors derived from Novartis compound I is described. Optimization of the P1, P3, and P1′ units led to the identification of 4-aminophenoxyacetic acid 24b with an IC50 value of 4.8 nM, which possessed an excell
