SCS-C006427

chevalone H

Pathway: Polyketides | Terpenoids Superclass: Meroterpenoids Class: Triketide meroterpenoids

Chemical Structure

Structure of chevalone H
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3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Download: SDF SMILES

Source Information

Aspergillus hiratsukae SCSIO 7S2001 (SCSIO 7S2001)
South China Sea
DOI: 10.3390/md20010071  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
488.6 Da
Threshold ≤ 500
ALogP
4.30
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
7
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C28H40O7
Molecular Weight:
488.6210 Da
SMILES:
CC(=O)O[C@H]1C[C@@H](O)[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@]2(C)Oc4cc(C)oc(=O)c4[C@@H](O)[C@@H]32)C1(C)C
InChIKey:
ZRLPBZGFEBTACK-PRWHYFDRSA-N
InChI:
InChI=1S/C28H40O7/c1-14-12-16-21(24(32)33-14)22(31)23-26(5)10-8-17-25(3,4)20(34-15(2)29)13-19(30)28(17,7)18(26)9-11-27(23,6)35-16/h12,17-20,22-23,30-31H,8-11,13H2,1-7H3/t17-,18-,19+,20-,22+,23-,26+,27-,28-/m0/s1
Calculated Properties
ALogP:
4.304 lipophilicity
TPSA:
106.20 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
7
Rotatable Bonds:
1
Ring Count:
5 (1 aromatic)
Chiral Centers:
9
Fsp³:
0.7857 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006427
NPClassifier Pathway:
Polyketides Terpenoids
NPClassifier Superclass:
Meroterpenoids
NPClassifier Class:
Triketide meroterpenoids
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

Activity values are displayed only when a quantitative or clearly reported result is available. Tested organisms, cell lines and molecular targets are shown under Target / model.
Activity Assay Target / model Result Reference
Antibacterial MIC Micrococcus lutea, methicillin-resistant Staphylococcus aureus, Streptococcus faecalis 6.25 μg/mL 10.3390/md20010071 Marine Drugs
Structure enlarged