SCS-C006695

cnidimol J

Pathway: Polyketides Superclass: Chromanes Class: Chromones

Chemical Structure

Structure of cnidimol J
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Source Information

Aspergillus versicolor (coral-associated fungus)
South China Sea
DOI: 10.3390/md23110429  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
276.2 Da
Threshold ≤ 500
ALogP
1.80
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
6
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C14H12O6
Molecular Weight:
276.2440 Da
SMILES:
COC(=O)c1cc2oc(C)cc(=O)c2c(O)c1C(C)=O
InChIKey:
BQSOKVZKAZZAIJ-UHFFFAOYSA-N
InChI:
InChI=1S/C14H12O6/c1-6-4-9(16)12-10(20-6)5-8(14(18)19-3)11(7(2)15)13(12)17/h4-5,17H,1-3H3
Calculated Properties
ALogP:
1.796 lipophilicity
TPSA:
93.81 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
6
Rotatable Bonds:
2
Ring Count:
2 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.2143 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006695
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Chromanes
NPClassifier Class:
Chromones
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 inhibitory activity LPS-induced NF-κB pathway All of the compounds were tested for their inhibitory activities of LPS-induced NF-κB activation in RAW264.7 cells. Compounds 6–8 exhibited inhibition... 10.3390/md23110429 Marine Drugs
Structure enlarged