SCS-C000423

1-hydroxy-3-hydroxymethylanthraquinone

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

Chemical Structure

Structure of 1-hydroxy-3-hydroxymethylanthraquinone
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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

Trichoderma harzianum (NA)
South China Sea
DOI: 10.1039/c8ra04865g  · RSC Advances

Drug-likeness (Lipinski Ro5)

Molecular Weight
254.2 Da
Threshold ≤ 500
ALogP
1.66
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H10O4
Molecular Weight:
254.2410 Da
SMILES:
O=C1c2ccccc2C(=O)c2c(O)cc(CO)cc21
InChIKey:
UZLMVCOKWZNITE-UHFFFAOYSA-N
InChI:
InChI=1S/C15H10O4/c16-7-8-5-11-13(12(17)6-8)15(19)10-4-2-1-3-9(10)14(11)18/h1-6,16-17H,7H2
Calculated Properties
ALogP:
1.660 lipophilicity
TPSA:
74.60 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
4
Rotatable Bonds:
1
Ring Count:
3 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.0667 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000423
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
Antibacterial MIC S. aureus 25.0 μM 10.1039/c8ra04865g RSC Advances
Antitumor IC50 HepG2 9.39 μM 10.1039/c8ra04865g RSC Advances
Structure enlarged