Structure Database (LMSD)
Common Name
Hatomasterol
Systematic Name
5β,19-cycloergosta-22E-en-3β,6β,7α-triol
Synonyms
LM ID
LMST01031213
Formula
Exact Mass
Calculate m/z
430.344695
Sum Composition
Status
Active
3D model of Hatomasterol
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
unclassified Stylissa
(#2627146)
Demospongiae
(#6042)
New polyhydroxylated sterols stylisterols A-C and a novel 5,19-cyclosterol hatomasterol from the Okinawan marine sponge Stylissa sp.,
Steroids, 2005
Steroids, 2005
Pubmed ID:
15610898
String Representations
InChiKey (Click to copy)
CREDXYMKNYHUGY-BELGCLGYSA-N
InChi (Click to copy)
InChI=1S/C28H46O3/c1-16(2)17(3)6-7-18(4)20-8-9-21-23-22(11-12-26(20,21)5)27-13-10-19(29)14-28(27,15-27)25(31)24(23)30/h6-7,16-25,29-31H,8-15H2,1-5H3/b7-6+/t17-,18+,19-,20+,21-,22-,23-,24-,25+,26+,27-,28+/m0/s1
SMILES (Click to copy)
C1[C@@]23C[C@@]2([C@H](O)[C@@H](O)[C@@]2([H])[C@]4([H])CC[C@@]([H])([C@@]4(C)CC[C@@]23[H])[C@]([H])(C)/C=C/[C@H](C)C(C)C)C[C@@H](O)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
31
Rings
5
Aromatic Rings
Rotatable Bonds
4
Van der Waals Molecular Volume
454.89
Topological Polar Surface Area
60.69
Hydrogen Bond Donors
3
Hydrogen Bond Acceptors
3
logP
6.05
Molar Refractivity
125.73
Admin
Created at
19th Jul 2021
Updated at
19th Jul 2021