Structure Database (LMSD)

Common Name
Penicisteroid H
Systematic Name
16β-acetoxy-5α-ergosta-22E-en-3β,,6β,7β,triol
Synonyms
  • 16beta-acetoxy-3beta,,6beta,7beta-trihydroxy-5alpha-ergost-22E-ene
LM ID
LMST01031169
Formula
Exact Mass
Calculate m/z
490.365825
Sum Composition
Status
Active

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Penicillium granulatum (#395885)
Eurotiomycetes (#147545)
Steroids from the Deep-Sea-Derived Fungus Penicillium granulatum MCCC 3A00475 Induced Apoptosis via Retinoid X Receptor (RXR)-α Pathway.,
Mar Drugs, 2019
Pubmed ID: 30893778

String Representations

InChiKey (Click to copy)
XGCBEJNSJGKYKN-WIJDSFKRSA-N
InChi (Click to copy)
InChI=1S/C30H50O5/c1-16(2)17(3)8-9-18(4)26-24(35-19(5)31)15-22-25-21(11-13-30(22,26)7)29(6)12-10-20(32)14-23(29)27(33)28(25)34/h8-9,16-18,20-28,32-34H,10-15H2,1-7H3/b9-8+/t17-,18+,20-,21-,22-,23+,24-,25+,26-,27-,28+,29+,30-/m0/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)/C=C/[C@H](C)C(C)C)[C@@H](OC(C)=O)C[C@@]4([H])[C@]3([H])[C@@H](O)[C@@H](O)[C@@]2([H])C[C@@H](O)C1

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 35
Rings 4
Aromatic Rings 0
Rotatable Bonds 6
Van der Waals Molecular Volume 516.79
Topological Polar Surface Area 86.99
Hydrogen Bond Donors 3
Hydrogen Bond Acceptors 5
logP 6.12
Molar Refractivity 139.29

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Created at
26th Feb 2021
Updated at
26th Feb 2021