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CAS 474-69-1

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Lumisterol

Description:
Lumisterol, with the CAS number 474-69-1, is a sterol compound that is a derivative of vitamin D. It is primarily known for its role in the biosynthesis of vitamin D and is formed from the photochemical transformation of ergosterol or other sterols under ultraviolet light. Lumisterol is characterized by its unique structure, which includes a sterane backbone with specific functional groups that influence its biological activity. It is less biologically active than other forms of vitamin D, such as cholecalciferol, but it has been studied for its potential effects on calcium metabolism and immune function. Lumisterol is soluble in organic solvents but has limited solubility in water, which is typical for sterols. Its stability can be affected by light and heat, making storage conditions important for maintaining its integrity. Research into lumisterol continues, particularly regarding its potential health benefits and applications in nutrition and medicine.
Formula:C28H44O
InChI:InChI=1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-10,18-20,22,24-26,29H,11-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,26+,27+,28+/m0/s1
InChI key:InChIKey=DNVPQKQSNYMLRS-YAPGYIAOSA-N
SMILES:C[C@@]12[C@](C=3[C@]([C@@]4(C)C(=CC3)C[C@@H](O)CC4)(CC1)[H])(CC[C@@]2([C@@H](/C=C/[C@@H](C(C)C)C)C)[H])[H]
Synonyms:
  • (3beta,9beta,10alpha,22E)-ergosta-5,7,22-trien-3-ol
  • (3β,9β,10α,22E)-Ergosta-5,7,22-trien-3-ol
  • 9β,10α-Ergosta-5,7,22-trien-3-ol
  • 9β,10α-Ergosta-5,7,22-trien-3β-ol
  • 9β,10α-Ergosterol
  • Ergosta-5,7,22-trien-3-ol,(3b,9b,10a,22E)-
  • Lumisterol
  • Lumisterol<sub>2</sub>
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