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3,7-dihydroxycholan-24-oic acid, monosodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31687-65-7

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31687-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31687-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,8 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31687-65:
(7*3)+(6*1)+(5*6)+(4*8)+(3*7)+(2*6)+(1*5)=127
127 % 10 = 7
So 31687-65-7 is a valid CAS Registry Number.

31687-65-7Upstream product

31687-65-7Relevant academic research and scientific papers

Dansyl-labeled cholic acid as a tool to build speciation diagrams for the aggregation of bile acids

Gomez-Mendoza, Miguel,Marin, M. Luisa,Miranda, Miguel A.

, p. 14776 - 14780 (2012)

Bile acids (BAs) are a family of natural steroids biosynthesized from cholesterol in the liver that tend to form aggregates in solution. A fluorescent derivative of cholic acid, namely 3α-Dns-ChA, was employed as a reporter to establish the speciation diagrams of the most abundant BAs that can be found mainly in three microenvironments, solution, and primary and secondary aggregates. The developed methodology is based on the analysis of the combined steady-state and time-resolved experiments performed on 3α-Dns-ChA whose emission behavior was found to be strongly medium dependent. In particular, speciation diagrams of sodium glycocholate (NaGCh), sodium taurocholate (NaTCh), sodium chenodeoxycholate (NaCDCh), sodium glycochenodeoxycholate (NaGCDCh), sodium deoxycholate (NaDCh), and sodium ursodeoxycholate (NaUDCh) were successfully built up.

Synthesis, characterization and biological activity of hydroxyl- bisphosphonic analogs of bile acids

Bortolini, Olga,Fantin, Giancarlo,Fogagnolo, Marco,Rossetti, Stefano,Maiuolo, Loredana,Di Pompo, Gemma,Avnet, Sofia,Granchi, Donatella

experimental part, p. 221 - 229 (2012/07/28)

Bisphosphonates (BPs) are now the most widely used drugs for diseases associated with increased bone resorption, such as osteoporosis, and tumor bone diseases. A significant drawback of the BPs is their poor oral absorption that is enhanced by the presence of bile acid substituents in the bisphosphonate framework, with no toxic effects. A straightforward synthesis of bile acid-containing hydroxy-bisphosphonates and a full characterization of these pharmaceutically important molecules, including an evaluation of affinity and the mechanism of binding to hydroxyapatite, is presented. The biological activity of bile acid-containing bisphosphonate salts was determined using the neutral-red assay on the L929 cell line and primary cultures of osteoclasts. The bioactivity of the new compounds was found superior than bisphosphonates of established activity.

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