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700026P

Avanti

3β-hydroxy-7-oxo-5-cholestenoic acid

Avanti Polar Lipids

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Sinónimos:
(25R)-cholest-5-en-26-oic acid, 3β-hydroxy-7-oxo
Empirical Formula (Hill Notation):
C27H42O4
Número de CAS:
1246298-64-5
Peso molecular:
430.62
NACRES:
NA.25

Análisis

>99% (TLC)

formulario

powder

envase

pkg of 1 × 5 mg (700026P-5mg)

manufacturer/tradename

Avanti Polar Lipids

enviado en

dry ice

temp. de almacenamiento

−20°C

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Este artículo
700132P700133P700029P
3β-hydroxy-7-oxo-5-cholestenoic acid Avanti Polar Lipids

Avanti

700026P

3β-hydroxy-7-oxo-5-cholestenoic acid

3β,7α,25-trihydroxy-5-cholestenoic acid Avanti Polar Lipids 700132P, powder

Avanti

700132P

3β,7α,25-trihydroxy-5-cholestenoic acid

3β,25-OH-7-oxo-5-cholestenoic acid Avanti Polar Lipids 700133P, powder

Avanti

700133P

3β,25-OH-7-oxo-5-cholestenoic acid

3β,7β-dihydroxy-5-cholestenoic acid Avanti Polar Lipids

Avanti

700029P

3β,7β-dihydroxy-5-cholestenoic acid

form

powder

form

powder

form

powder

form

powder

packaging

pkg of 1 × 5 mg (700026P-5mg)

packaging

pkg of 1 × 1 mg (700132P-1mg)

packaging

pkg of 1 × 1 mg (700133P-1mg)

packaging

pkg of 1 × 1 mg (700029P-1mg)

manufacturer/tradename

Avanti Polar Lipids

manufacturer/tradename

Avanti Polar Lipids 700132P

manufacturer/tradename

Avanti Polar Lipids 700133P

manufacturer/tradename

Avanti Polar Lipids

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Descripción general

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).

Acciones bioquímicas o fisiológicas

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.

Envase

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

Código de clase de almacenamiento

11 - Combustible Solids

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Cholestenoic acids regulate motor neuron survival via liver X receptors
Theofilopoulos S, et al.
The Journal of Clinical Investigation, 124(11), 4829-4842 (2014)
Sterolomics in biology, biochemistry, medicine
Griffiths WJ and Wang Y
TrAC, Trends in Analytical Chemistry, 115280-115280 (2018)
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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