Structure Database (LMSD)
Common Name
Lamellosterol A
Systematic Name
3α,7α,8β-trihydroxy-5α-cholestane-26-sulfate
Synonyms
LM ID
LMST05020060
Status
Active
Exact Mass
Calculate m/z
516.312077
Formula
Abbrev
Main
Classification
String Representations
InChiKey (Click to copy)
UHZPZECSBHKZCG-FVZADQOOSA-N
InChi (Click to copy)
InChI=1S/C27H48O7S/c1-17(16-34-35(31,32)33)6-5-7-18(2)21-8-9-22-26(21,4)13-11-23-25(3)12-10-20(28)14-19(25)15-24(29)27(22,23)30/h17-24,28-30H,5-16H2,1-4H3,(H,31,32,33)/t17?,18-,19-,20-,21-,22-,23-,24-,25+,26-,27-/m1/s1
SMILES (Click to copy)
C1C[C@@H](O)C[C@]2([H])C[C@@H](O)[C@@]3(O)[C@]4([H])CC[C@]([H])([C@H](C)CCCC(C)COS(=O)(O)=O)[C@@]4(C)CC[C@]3([H])[C@@]12C
References
Reference
Anti-prion and α-Synuclein Aggregation Inhibitory Sterols from the Sponge Lamellodysidea cf. chlorea.
J Nat Prod, 2020
DOI: 10.1021/acs.jnatprod.0c01168
PMID: 33269586
J Nat Prod, 2020
DOI: 10.1021/acs.jnatprod.0c01168
PMID: 33269586
Taxonomy Information
Calculated Physicochemical Properties
Heavy Atoms
35
Rings
4
Aromatic Rings
0
Rotatable Bonds
8
Van der Waals Molecular Volume
506.26
Topological Polar Surface Area
124.29
Hydrogen Bond Donors
4
Hydrogen Bond Acceptors
7
logP
6.75
Molar Refractivity
135.69
Admin
Created at
7th Dec 2020
Updated at
7th Dec 2020