Structure Database (LMSD)

HO OH OH OH H H H
Common Name
(23S,25R)-23,25,26-trihydroxyvitamin D3
Systematic Name
(5Z,7E)-(3S,23S,25R)-9,10-seco-5,7,10(19)-cholestatriene-3,23,25,26-tetrol
Synonyms
  • (23S,25R)-23,25,26-trihydroxycholecalciferol
LM ID
LMST03020299
Formula
Exact Mass
Calculate m/z
432.32396
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
GDIBDBUYVICGLY-CLKUJDLHSA-N
InChi (Click to copy)
InChI=1S/C27H44O4/c1-18-7-10-22(29)15-21(18)9-8-20-6-5-13-27(4)24(11-12-25(20)27)19(2)14-23(30)16-26(3,31)17-28/h8-9,19,22-25,28-31H,1,5-7,10-17H2,2-4H3/b20-8+,21-9-/t19-,22+,23+,24-,25+,26-,27-/m1/s1
SMILES (Click to copy)
C1C(=C)/C(=C\C=C2\[C@]3([H])CC[C@@]([H])([C@@]3(C)CCC\2)[C@]([H])(C)C[C@H](O)C[C@](O)(C)CO)/C[C@@H](O)C1

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Gallus gallus (#9031)
23, 25, 26-trihydroxycholecalciferol. A 25-hydroxycholecalciferol-26,23-lactone precursor.,
Biochem J, 1982
Pubmed ID: 7126191

Other Databases

CHEBI ID
LIPIDBANK ID
VVD0326
PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 31
Rings 3
Aromatic Rings 0
Rotatable Bonds 7
Van der Waals Molecular Volume 465.82
Topological Polar Surface Area 80.92
Hydrogen Bond Donors 4
Hydrogen Bond Acceptors 4
logP 5.82
Molar Refractivity 127.48

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Created at
-
Updated at
27th Mar 2024