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all-trans-(R)-13,14-Dihydroretinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1007220-97-4

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1007220-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007220-97-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,2,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1007220-97:
(9*1)+(8*0)+(7*0)+(6*7)+(5*2)+(4*2)+(3*0)+(2*9)+(1*7)=94
94 % 10 = 4
So 1007220-97-4 is a valid CAS Registry Number.

1007220-97-4Downstream Products

1007220-97-4Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR TREATING METABOLIC DISEASES

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Page/Page column 26, (2008/12/05)

A pharmaceutical composition for treating a metabolic disease in a mammalian subject includes a therapeutically effective amount of all-trans-13,14-dihydroretinoid, all-trans-13,14-dihydroretinoid derivative, or agent capable of modulating the level of at least one all-trans-13,14-dihydroretinoid or all-trans-13,14-dihydroretinoid derivative in the subject.

Stereospecificity of retinol saturase: Absolute configuration, synthesis, and biological evaluation of dihydroretinoids

Moise, Alexander R.,Dominguez, Marta,Alvarez, Susana,Alvarez, Rosana,Schupp, Michael,Cristancho, Ana G.,Kiser, Philip D.,De Lera, Angel R.,Lazar, Mitchell A.,Palczewski, Krzysztof

, p. 1154 - 1155 (2008/10/09)

Retinol saturase carries out a stereospecific saturation of the C13-C14 double bond of all-trans-retinol to generate (13R)-all-trans-13,14-dihydroretinol. This compound is found in cells expressing mouse or zebrafish retinol saturase and in the livers of mice fed retinyl palmitate. All-trans-13,14-dihydroretinol is oxidized in vivo to all-trans-13,14-dihydroretinoic acid, a highly selective agonist of the retinoic acid receptor. The naturally occurring (13R)-all-trans-13,14-dihydroretinoic acid is a weaker agonist than the (13S) enantiomer, indicating enantioselective recognition by the ligand-binding pocket of this receptor. Consequently the (13S) enantiomer, acting through the retinoic acid receptor, also inhibits adipose differentiation more potently than the (13R) enantiomer. Copyright

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