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1-Piperidinecarboxylic acid, 4-(aminomethyl)-4-cyclohexyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

312638-96-3

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312638-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312638-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,6,3 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 312638-96:
(8*3)+(7*1)+(6*2)+(5*6)+(4*3)+(3*8)+(2*9)+(1*6)=133
133 % 10 = 3
So 312638-96-3 is a valid CAS Registry Number.

312638-96-3Relevant academic research and scientific papers

THIAZOLYL COMPOUNDS USEFUL AS KINASE INHIBITORS

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, (2008/12/04)

The invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof. The formula I thiazolyl compounds inhibit tyrosine kinase activity thereby making them useful as anticancer agents and for the treatment of Alzheimer's disease

Optimization of a privileged structure leading to potent and selective human melanocortin subtype-4 receptor ligands

Bakshi, Raman K.,Hong, Qingmei,Tang, Rui,Kalyani, Rubana N.,MacNeil, Tanya,Weinberg, David H.,Van Der Ploeg, Lex H. T.,Patchett, Arthur A.,Nargund, Ravi P.

, p. 1130 - 1133 (2007/10/03)

Design and synthesis of potent MC4 selective agonists based on cyclohexylpiperidine derived cyclic urea, oxazolidinones, and sulfonamide based privileged structures are disclosed.

MELANOCORTIN RECEPTOR AGONISTS

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Page/Page column 38, (2010/02/11)

The present invention relates a compound of formula 1, and pharmaceutically acceptable salt, hydrate, solvate, or isomer thereof effective as agonist of melanocortin receptor, and an agonistic composition of melanocortin receptor comprising the same as active ingredient.

Substituted piperidines as melanocortin-4 receptor agonists

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Page column 51, (2010/02/05)

Certain novel substituted piperidine compounds are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction. Also provided are methods of treating sexual dysfunction with a compound that is a selective agonist of MC-4R over any other human melanocortin receptor.

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