Structure Database (LMSD)

Common Name
Xidaosteroid A
Systematic Name
17α-hydroperoxy-23R-Methyl-ergosta-5,20(21)-diene-3β-ol
Synonyms
LM ID
LMST01031275
Formula
C29H48O3
Exact Mass
Calculate m/z
444.360345
Sum Composition
ST 29:2;O3
Status
Active
Show lipids differing only in stereochemistry/bond geometry

Classification

Category
Main Class
Sub Class
Sterol Lipids [ST]
Sterols [ST01]
Ergosterols and C24-methyl derivatives [ST0103]

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Rumphella (#1267119)
Anthozoa (#6101)
Structural diversity of bioactive steroid compounds isolated from soft corals in the period 2015-2020.,
J Steroid Biochem Mol Biol, 2022
Pubmed ID: 35031429

String Representations

InChiKey (Click to copy)
NRNCFLCPJOOIIQ-STJZTYAPSA-N
InChi (Click to copy)
InChI=1S/C29H48O3/c1-18(2)21(5)19(3)16-20(4)29(32-31)15-12-26-24-9-8-22-17-23(30)10-13-27(22,6)25(24)11-14-28(26,29)7/h8,18-19,21,23-26,30-31H,4,9-17H2,1-3,5-7H3/t19-,21-,23+,24-,25+,26+,27+,28+,29+/m1/s1
SMILES (Click to copy)
C1C[C@H](O)CC2=CC[C@@]3([H])[C@]4([H])CC[C@](OO)(C(=C)C[C@@H](C)[C@H](C)C(C)C)[C@@]4(C)CC[C@]3([H])[C@@]12C

Other Databases

PubChem CID
171121374

Calculated Physicochemical Properties

Heavy Atoms 32
Rings 4
Aromatic Rings
Rotatable Bonds 6
Van der Waals Molecular Volume 481.91
Topological Polar Surface Area 49.69
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 3
logP 8.16
Molar Refractivity 131.96

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Created at
14th Feb 2022
Updated at
14th Feb 2022