700103 | cholest-4-en-3-one-d7

cholest-4-en-3-one-d7

cholest-4-en-3-one-d7

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1mg 700103P-1mg 700103P-1mg 1 x 1mg $458.42
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Info

cholest-4-en-3-one-d7

cholest-4-en-3-one-d7

Cholest-4-en-3-one-d7 is a deuterated form of cholest-4-en-3-one, meaning that a hydrogen atom has been replaced with a deuterium atom - deuterium is one of the two heavy and stable isotopes of hydrogen.

Cholest-4-en-3-one is a cholest-4-ene substituted by an oxo- group at the 3rd position. It’s a cholestanoid and a human and plant metabolite. The compound is derived from cholesterol as a result of cholesterol oxidation and isomerization, processes catalyzed by cholesterol oxidase - a bacterial flavoenzyme.

Cholest-4-en-3-one acts as an important synthetic intermediate detergent in various steroid transformations.

Studies show promising evidence that the metabolite has potent effects against obesity, liver disease, and keratinization.

Cholest-4-en-3-one is also found to play a role as a precursor in the production of drug intermediates, including androsta-1,4-diene-3,17-dione or androst-4-ene-3,17-dione, which are crucial starting resources for the synthesis of anabolic drugs and contraceptive hormones.

The cholestanoid has some derivatives, like the new developing drug Olesoxime (cholest-4-en-3-one, oxime) that displays neuroprotective properties in the therapy of spinal muscular atrophy.

The isotope-labeled variation of the cholesterol derivative, Cholest-4-en-3-one-d7 is intended for use as an internal standard for the quantification of cholest-4-en-3-one.

Avanti Polar Lipids synthesizes high-grade Cholest-4-en-3-one-d7 to support science laboratories and research projects worldwide.

Data
Hygroscopic
No
Light Sensitive
No
Molecular Formula

C27H37D7O

Percent Composition

C 82.79%, H 13.12%, O 4.08%

Purity
%gt;99%
Stability
1 Year
Storage Temperature
-20C
CAS Number
2389048-48-8
CAS Registry Number is a Registered Trademark of the American Chemical Society
Formula Weight
391.69
Exact Mass
391.38
Certificates of Analysis

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