SCS-C006165

5-hydroxy-3-hydroxymethyl-2-methyl-7-methoxychromone

Pathway: Polyketides Superclass: Chromanes Class: Chromones

Chemical Structure

Structure of 5-hydroxy-3-hydroxymethyl-2-methyl-7-methoxychromone
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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 spelaeus (NA)
Kingdom Fungi Phylum Ascomycota Class Eurotiomycetes Order Eurotiales Family Aspergillaceae Genus Aspergillus Species Aspergillus spelaeus
South China Sea  · 21.573° N, 109.767° E
DOI: 10.3390/md23060251  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
236.2 Da
Threshold ≤ 500
ALogP
1.31
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C12H12O5
Molecular Weight:
236.2230 Da
SMILES:
COc1cc(O)c2c(=O)c(CO)c(C)oc2c1
InChIKey:
VNPAXPBNMQPWKD-UHFFFAOYSA-N
InChI:
InChI=1S/C12H12O5/c1-6-8(5-13)12(15)11-9(14)3-7(16-2)4-10(11)17-6/h3-4,13-14H,5H2,1-2H3
Calculated Properties
ALogP:
1.308 lipophilicity
TPSA:
79.90 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
5
Rotatable Bonds:
2
Ring Count:
2 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.2500 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006165
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
Enzyme inhibition inhibition rate PDE4 compounds 2, 3, 5, 8, 9, 11–14, and 16 exhibited weak PDE4 inhibitory activity at a concentration of 10 μM 10.3390/md23060251 Marine Drugs
Antitumor cytotoxicity screening in vitro anticancer activity screen compounds 1–4, 7–9, 11, and 15–21 were screened for anticancer activity in vitro 10.3390/md23060251 Marine Drugs
Structure enlarged