Structure Database (LMSD)
Common Name
Stelliferasterol
Systematic Name
26-methylstigmasta-5,25E-dien-3β-ol
Synonyms
No other lipid differing only in stereochemistry/bond geometry found
3D model of Stelliferasterol
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
Jaspis
(#1336932)
Demospongiae
(#6042)
Minor and Trace Sterols in Marine Invertebrates. 8.1 Isolation, Structure Elucidation, and Partial Synthesis of Two Novel Sterols—Stelliferasterol and Isostelliferasterol,
J Am Chem Soc, 1978
J Am Chem Soc, 1978
DOI:
10.1021/ja00492a041
String Representations
InChiKey (Click to copy)
VXPPHQIHBBYPMQ-DPPABISVSA-N
InChi (Click to copy)
InChI=1S/C30H50O/c1-7-20(3)22(8-2)10-9-21(4)26-13-14-27-25-12-11-23-19-24(31)15-17-29(23,5)28(25)16-18-30(26,27)6/h7,11,21-22,24-28,31H,8-10,12-19H2,1-6H3/b20-7+/t21-,22-,24+,25+,26-,27+,28+,29+,30-/m1/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CC[C@@H](CC)/C(=C/C)/C)CC[C@@]4([H])[C@]3([H])CC=C2C[C@@H](O)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
31
Rings
4
Aromatic Rings
0
Rotatable Bonds
6
Van der Waals Molecular Volume
481.63
Topological Polar Surface Area
20.23
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
1
logP
8.62
Molar Refractivity
133.32
Admin
Created at
-
Updated at
30th Sep 2021