Structure Database (LMSD)
Common Name
Panuosterone
Systematic Name
2β,3β,14α,20R,22R,24S-hexahydroxy-5β-ergost-7-en-6-one
Synonyms
LM ID
LMST01031297
Formula
Exact Mass
Calculate m/z
494.324355
Sum Composition
Status
Curated
3D model of Panuosterone
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
Tapinella panuoides
(#80604)
Agaricomycetes
(#155619)
Ecdysteroid constituents of the mushroom Tapinella panuoides,
Phytochemistry, 1998
Phytochemistry, 1998
Aspergillus puniceus
(#41744)
Eurotiomycetes
(#147545)
Punicesterones A-G, polyhydroxylated mycoecdysteroids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021.,
Phytochemistry, 2022
Phytochemistry, 2022
Pubmed ID:
36372238
String Representations
InChiKey (Click to copy)
YXPVYQIMXPYFSF-DQVFBYKJSA-N
InChi (Click to copy)
InChI=1S/C28H46O7/c1-15(2)26(5,33)14-23(32)27(6,34)22-8-10-28(35)17-11-19(29)18-12-20(30)21(31)13-24(18,3)16(17)7-9-25(22,28)4/h11,15-16,18,20-23,30-35H,7-10,12-14H2,1-6H3/t16-,18-,20+,21-,22-,23+,24+,25+,26+,27+,28+/m0/s1
SMILES (Click to copy)
C12=CC(=O)[C@]3([H])C[C@@H](O)[C@@H](O)C[C@]3(C)[C@@]1([H])CC[C@]1(C)[C@@]([H])([C@@](C)(O)[C@H](O)C[C@](O)(C)C(C)C)CC[C@@]21O
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
35
Rings
4
Aromatic Rings
Rotatable Bonds
5
Van der Waals Molecular Volume
499.77
Topological Polar Surface Area
138.45
Hydrogen Bond Donors
6
Hydrogen Bond Acceptors
7
logP
3.82
Molar Refractivity
134.22
Admin
Created at
21st Nov 2022
Updated at
21st Nov 2022