| Identification | Back Directory |  [Name]
  (25R)-cholest-5-en-26-oic acid, 3,7-hydroxy |  [CAS]
  1246298-66-7 |  [Synonyms]
  7-dihydroxy-5-cholestenoic acid 3β,7β-dihydroxy -5-cholestenoic acid 3ss,7ss-dihydroxy-5-cholestenoic acid (25R)-cholest-5-en-26-oic acid, 3,7-hydroxy (25R)-cholest-5-en-26-oic acid, 3β,7β-hydroxy Cholest-5-en-26-oic acid, 3,7-dihydroxy-, (3β,7β,25R)- (25R) - Cholester-5-ene-26-oleic acid, 3?, 7- hydroxyl (25R)-CHOLEST-5-EN-26-OIC ACID, 3,7-HYDROXY;3;7-DIHYDROXY-5-CHOLESTENOIC ACID |  [Molecular Formula]
  C27H44O4 |  [MOL File]
  1246298-66-7.mol |  [Molecular Weight]
  432.636 |  
 | Chemical Properties | Back Directory |  [Boiling point ]
  588.1±35.0 °C(Predicted) |  [density ]
  1.12±0.1 g/cm3(Predicted) |  [storage temp. ]
  -20°C |  [form ]
  powder |  [pka]
  4.81±0.21(Predicted) |  
 | Hazard Information | Back Directory |  [Uses]
  3β,7β-dihydroxy-5-cholestenoic acid may be used as an authentic diastereoisomer standard in mass spectrometry (MS) experiments. |  [General Description]
  3β,7β-dihydroxy-5-cholestenoic acid (3β,7β-diHCA) is associated with plasma and is a C27 acid. 3β,7β-diHCA is synthesized from 3β-hydroxy-7-oxocholest-5-en-(25R)26-oic acid (3βH,7O-CA) by the action of the enzyme hydroxysteroid 11-β dehydrogenase 1. |  [Biochem/physiol Actions]
  3β,7β-dihydroxy-5-cholestenoic acid (3β,7β-diHCA) levels are elevated in Niemann-Pick type C (NPC) disease and Niemann-Pick (NP) disease type B disorders. It elicits toxicity to oculomotor neurons. |  
  
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                                Merck KGaA  
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                                Creative Enzymes  
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