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(S)-4-((R)-4-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-pentyl)-2,2,4-trimethyl-[1,3]dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93511-78-5

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  • (S)-4-((R)-4-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-pentyl)-2,2,4-trimethyl-[1,3]dioxolane

    Cas No: 93511-78-5

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  • (S)-4-((R)-4-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-pentyl)-2,2,4-trimethyl-[1,3]dioxolane

    Cas No: 93511-78-5

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93511-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93511-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,1 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93511-78:
(7*9)+(6*3)+(5*5)+(4*1)+(3*1)+(2*7)+(1*8)=135
135 % 10 = 5
So 93511-78-5 is a valid CAS Registry Number.

93511-78-5Relevant articles and documents

Chemical Synthesis of Side-Chain-Hydroxylated Vitamin D3 Derivatives and Their Metabolism by CYP27B1

Iwaki, Miho,Mizumoto, Yuka,Nagasawa, Kazuo,Nagata, Akiko,Ohshita, Haruki,Sakaki, Toshiyuki,Sakamoto, Ryota,Yasuda, Kaori

, p. 2896 - 2900 (2021/07/31)

1α,25-Dihydroxyvitamin D3 (abbreviated here as 1,25D3) is a hormonally active form of vitamin D3 (D3), and is produced from D3 by CYP27 A1-mediated hydroxylation at C25, followed by CYP27B1-mediated hydroxylation at C1. Further hydroxylation of 25D3 and 1,25D3 occurs at C23, C24 and C26 to generate corresponding metabolites, except for 1,25R,26D3. Since the capability of CYP27B1 to hydroxylate C1 of side-chain-hydroxylated metabolites other than 23S,25D3 and 24R,25D3 has not been examined, we have here explored the role of CYP27B1 in the C1 hydroxylation of a series of side-chain-hydroxylated D3 derivatives. We found that CYP27B1 hydroxylates the R diastereomers of 24,25D3 and 25,26D3 more effectively than the S diastereomers, but shows almost no activity towards either diastereomer of 23,25D3. This is the first report to show that CYP27B1 metabolizes 25,26D3 to the corresponding 1α-hydroxylated derivative, 1,25,26D3. It will be interesting to examine the physiological relevance of this finding.

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