SCS-C006562

carneusone F

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Anthraquinones and anthrones

Chemical Structure

Structure of carneusone F
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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 carneus GXIMD00543 (NA)
Kingdom Fungi Phylum Ascomycota Class Eurotiomycetes Order Eurotiales Family Aspergillaceae Genus Aspergillus Species Aspergillus carneus
South China Sea
DOI: 10.3390/md22020063  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
370.4 Da
Threshold ≤ 500
ALogP
2.31
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
7
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C20H18O7
Molecular Weight:
370.3570 Da
SMILES:
Cc1cc(O)c2c3c1C[C@@H]1O[C@]3(OC1(C)C)c1cc(O)c(O)c(O)c1C2=O
InChIKey:
RMJZNXQLJKMPET-YUNKPMOVSA-N
InChI:
InChI=1S/C20H18O7/c1-7-4-10(21)14-15-8(7)5-12-19(2,3)27-20(15,26-12)9-6-11(22)16(23)18(25)13(9)17(14)24/h4,6,12,21-23,25H,5H2,1-3H3/t12-,20-/m0/s1
Calculated Properties
ALogP:
2.313 lipophilicity
TPSA:
116.45 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
7
Rotatable Bonds:
0
Ring Count:
5 (2 aromatic)
Chiral Centers:
2
Fsp³:
0.3500 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006562
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Polycyclic aromatic polyketides
NPClassifier Class:
Anthraquinones and anthrones
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
Anti-inflammatory NO secretion inhibition nitric oxide production 20.2 μM 10.3390/md22020063 Marine Drugs
Structure enlarged