Structure Database (LMSD)
Common Name
(22E)-(25S)-1alpha,25,26-trihydroxy-22,23-didehydrovitamin D3
Systematic Name
(5Z,7E,22E)-(1S,3R,25S)-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,25,26-tetrol
Synonyms
- (22E)-(25S)-1alpha,25,26-trihydroxy-22,23-didehydrocholecalciferol
3D model of (22E)-(25S)-1alpha,25,26-trihydroxy-22,23-didehydrovitamin D3
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
synthetic construct
(#32630)
Synthesis of 1a,25S,26-Trihydroxy-D22-cholecalciferol, A Potent Inducer of Cell Differentiation
String Representations
InChiKey (Click to copy)
JYHXCOMHKCOBKF-NIIDVMHZSA-N
InChi (Click to copy)
InChI=1S/C27H42O4/c1-18(7-5-13-26(3,31)17-28)23-11-12-24-20(8-6-14-27(23,24)4)9-10-21-15-22(29)16-25(30)19(21)2/h5,7,9-10,18,22-25,28-31H,2,6,8,11-17H2,1,3-4H3/b7-5+,20-9+,21-10-/t18-,22-,23-,24+,25+,26+,27-/m1/s1
SMILES (Click to copy)
[C@@H]1(O)C(=C)/C(=C\C=C2\[C@]3([H])CC[C@@]([H])([C@@]3(C)CCC\2)[C@]([H])(C)/C=C/C[C@@](O)(C)CO)/C[C@@H](O)C1
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
31
Rings
3
Aromatic Rings
0
Rotatable Bonds
6
Van der Waals Molecular Volume
463.18
Topological Polar Surface Area
80.92
Hydrogen Bond Donors
4
Hydrogen Bond Acceptors
4
logP
5.60
Molar Refractivity
127.38
Admin
Created at
-
Updated at
3rd Oct 2024