(1S,3Z)-3-{2-[(1R,3aS,4E,7aR)-1-[(2R)-6-hydroxy-6-(2H3)methyl(7,7,7-2H3)heptan-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

• ChemBase ID: 163538
• Molecular Formular: C27H44O2
• Molecular Mass: 400.63706
• Monoisotopic Mass: 400.33413065
• SMILES: C1C/C(=C\C=C/2\C[C@H](CCC2=C)O)/[C@H]2[C@](C1)([C@H](CC2)[C@@H](CCCC(O)(C)C)C)C
• Canonical SMILES: O[C@H]1CCC(=C)/C(=C\C=C\2/CCC[C@]3([C@H]2CC[C@@H]3[C@@H](CCCC(O)(C)C)C)C)/C1
• InChI: InChI=1S/C27H44O2/c1-19-10-13-23(28)18-22(19)12-11-21-9-7-17-27(5)24(14-15-25(21)27)20(2)8-6-16-26(3,4)29/h11-12,20,23-25,28-29H,1,6-10,13-18H2,2-5H3/b21-11+,22-12-/t20-,23+,24-,25+,27-/m1/s1
• InChIKey: JWUBBDSIWDLEOM-DTOXIADCSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: (1S,3Z)-3-{2-[(1R,3aS,4E,7aR)-1-[(2R)-6-hydroxy-6-(^2H₃)methyl(7,7,7-^2H₃)heptan-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
• IUPAC Traditional name: (1S,3Z)-3-{2-[(1R,3aS,4E,7aR)-1-[(2R)-6-hydroxy-6-(^2H₃)methyl(7,7,7-^2H₃)heptan-2-yl]-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
• Synonyms: (3β,5Z,7E)-9,10-Secocholesta-5,7,10(19)-triene-3,25-diol-d6; 25-Hydroxycholecalciferol-d6; 25-Hydroxyvitamin D-d6; 25-Hydroxyvitamin D3-d6; Calcidiol-d6; Didrogyl-d6; Hidroferol-d6; Ro 8-8892-d6; Calcifediol-d6

Database IDs

• CAS Number: 78782-98-6
• PubChem SID: 162257673
• PubChem CID: 66577010

CALCULATED PROPERTIES

• Acid pKa: 18.384342
• H Acceptors: 2
• H Donor: 2
• LogD (pH = 5.5): 5.654346
• LogD (pH = 7.4): 5.654346
• Log P: 5.654346
• Molar Refractivity: 125.0606 cm^3
• Polarizability: 48.829468 Å^3
• Polar Surface Area: 40.46 Å^2
• Rotatable Bonds: 6
• Lipinski's Rule of Five: false

PROPERTIES

Physical Property

• Solubility: Chloroform; Ethyl Acetate
• Apperance: White Solid
• Melting Point: 64-69°C

Safety Information

• Storage Condition: Amber Vial, -86?C Freezer, Under Inert Atmosphere

DETAILS

Toronto Research Chemicals - C125702

A metabolite of Vitamin D. The principal circulating form of vitamin D3, formed in the liver by hydroxylation at C-25. Calcium regulator.

REFERENCES

• orii, et al.: Arch. Biochem. Biophys., 120, 513 (1967)
• Blunt, et al.: Biochemistry, 7, 3317 (1967)
• Liu, et al.: Science, 311, 1770 (1967)