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700026P

Avanti

3β-hydroxy-7-oxo-5-cholestenoic acid

Avanti Polar Lipids 700026P, powder

Synonym(s):
(25R)-cholest-5-en-26-oic acid, 3β-hydroxy-7-oxo
Empirical Formula (Hill Notation):
C27H42O4
CAS Number:
Molecular Weight:
430.62
NACRES:
NA.25

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 5 mg (700026P-5mg)

manufacturer/tradename

Avanti Polar Lipids 700026P

shipped in

dry ice

storage temp.

−20°C

General description

Cholestenoic acids are cholesterol metabolic intermediates and precursors to bile acids. 3β-hydroxy-7-oxo-5-cholestenoic acid is synthesized from 7β-hydroxycholesterol. The enzymes for synthesis of cholestenoic acids are majorly present in the central nervous system (CNS) of mammals. 3β-hydroxy-7-oxo-5-cholestenoic acid (3βH,7O-CA) is also synthesized from 26-hydroxy-7-oxocholesterol by the action of the enzyme cytochrome P450 family 27 subfamily A member 1 sterol 27-hydroxylase (CYP27A1).

Biochem/physiol Actions

3β-hydroxy-7-oxocholest-5-en-26-oic acid (3βH,7O-CA) acts as a ligand for liver X receptors (LXR) and activates them at micromolar concentration. 3βH,7O-CA favors the islet-1+ cells synthesis and islet-1–GFP expression. 3βH,7O-CA also mediates oculomotor neurons maturation and its conversion to 3β,7β-dihydroxycholest-5-en-(25S)26-oic acid (3β,7β-diHCA) is catalyzed by the enzyme hydroxysteroid 11-β dehydrogenase.

Packaging

5 mL Amber Glass Screw Cap Vial (700026P-5mg)

Storage Class Code

13 - Non Combustible Solids

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

More Documents

Quotes and Ordering

Sterolomics in biology, biochemistry, medicine
Griffiths WJ and Wang Y
TrAC, Trends in Analytical Chemistry, 115280-115280 (2018)
Cholestenoic acids regulate motor neuron survival via liver X receptors
Theofilopoulos S, et al.
The Journal of Clinical Investigation, 124(11), 4829-4842 (2014)
Identification of unusual oxysterols and bile acids with 7-oxo or 3beta, 5alpha, 6beta-trihydroxy functions in human plasma by charge-tagging mass spectrometry with multistage fragmentation
Griffiths WJ, et al.
Journal of Lipid Research, 59(6), 1058-1070 (2018)
27-Hydroxylated Low Density Lipoprotein (LDL) Cholesterol Can Be Converted to 7alpha, 27-Dihydroxy-4-cholesten-3-one (Cytosterone) before Suppressing Cholesterol Production in Normal Human Fibroblasts EVIDENCE THAT AN ALTERED METABOLISM OF LDL CHOLESTEROL
Axelson M and Larsson O
The Journal of Biological Chemistry, 271(22), 12724-12736 (1996)

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