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1296211-56-7

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1296211-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1296211-56-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,6,2,1 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1296211-56:
(9*1)+(8*2)+(7*9)+(6*6)+(5*2)+(4*1)+(3*1)+(2*5)+(1*6)=157
157 % 10 = 7
So 1296211-56-7 is a valid CAS Registry Number.

1296211-56-7Relevant articles and documents

ISOXAZOLE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF

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Paragraph 0117; 0120-0121, (2020/11/26)

The present invention generally relates to an isoxazole derivative, a preparation therefor, and a use thereof. In particular, the present invention provides a farnesoid X receptor (FXR) agonist compound, and a stereoisomer, a tautomer, a polymorph, a solvate (e.g., a hydrate), a pharmaceutically acceptable salt, an ester, a metabolite, and an N-oxide, and the chemically protected forms and prodrugs thereof. The present invention further provides a preparation method for the compound, an intermediate thereof, and a pharmaceutical composition and kit containing the same and used thereof for treating FXR-mediated diseases or conditions.

Discovery of 6-(4-{[5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl]methoxy}piperidin-1-yl)-1-methyl-1H-indole-3-carboxylic Acid: A Novel FXR Agonist for the Treatment of Dyslipidemia

Genin, Michael J.,Bueno, Ana B.,Agejas Francisco, Javier,Manninen, Peter R.,Bocchinfuso, Wayne P.,Montrose-Rafizadeh, Chahrzad,Cannady, Ellen A.,Jones, Timothy M.,Stille, John R.,Raddad, Eyas,Reidy, Charles,Cox, Amy,Michael, M. Dodson,Michael, Laura F.

, p. 9768 - 9772 (2016/01/12)

The farnesoid X receptor (FXR) is a member of the "metabolic" subfamily of nuclear receptors. Several FXR agonists have been reported in the literature to have profound effects on plasma lipids in animal models. To discover novel and effective therapies for dyslipidemia and atherosclerosis, we have developed a series of potent FXR agonists that robustly lower plasma LDL and vLDL in LDLr-/- mice. To this end the novel piperidinylisoxazole system LY2562175 was discovered. This molecule is a potent and selective FXR agonist in vitro and has robust lipid modulating properties, lowering LDL and triglycerides while raising HDL in preclinical species. The preclinical ADME properties of LY2562175 were consistent with enabling once daily dosing in humans, and it was ultimately advanced to the clinic for evaluation in humans. The synthesis and biological profile of this molecule is discussed.

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