Structure Database (LMSD)
Common Name
Gerardiasterone
Systematic Name
2β,3β,14α,20R,22R,23S,25-heptahydroxy-5β-cholest-7-en-6-one
Synonyms
LM ID
LMST01010577
Formula
Exact Mass
Calculate m/z
496.30362
Sum Composition
Status
Active
No other lipid differing only in stereochemistry/bond geometry found
3D model of Gerardiasterone
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
Savalia savaglia
(#328566)
Anthozoa
(#6101)
Gerardiasterone, a new ecdysteroid with a 20,22,23,25-tetrahydroxylated side chain from the mediterranean zoanthid Gerardia savaglia,
J Chem Soc Chem Commun, 1986
J Chem Soc Chem Commun, 1986
DOI:
10.1039/C39860000040
String Representations
InChiKey (Click to copy)
SLAXZVJCSMNNPH-MLXSIWSOSA-N
InChi (Click to copy)
InChI=1S/C27H44O8/c1-23(2,33)12-20(31)22(32)26(5,34)21-7-9-27(35)15-10-17(28)16-11-18(29)19(30)13-24(16,3)14(15)6-8-25(21,27)4/h10,14,16,18-22,29-35H,6-9,11-13H2,1-5H3/t14-,16-,18+,19-,20-,21-,22+,24+,25+,26+,27+/m0/s1
SMILES (Click to copy)
C12=CC([C@]3([H])C[C@@H](O)[C@@H](O)C[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2(O)CC[C@@]1([C@](O)(C)[C@H](O)[C@@H](O)CC(O)(C)C)[H])=O
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
35
Rings
4
Aromatic Rings
Rotatable Bonds
5
Van der Waals Molecular Volume
491.26
Topological Polar Surface Area
158.68
Hydrogen Bond Donors
7
Hydrogen Bond Acceptors
8
logP
2.83
Molar Refractivity
131.58
Admin
Created at
12th Jul 2023
Updated at
12th Jul 2023