SCS-C000420

pachybasin

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

Chemical Structure

Structure of pachybasin
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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
238.2 Da
Threshold ≤ 500
ALogP
2.48
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
3
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H10O3
Molecular Weight:
238.2400 Da
SMILES:
Cc1cc(O)c2c(c1)C(=O)c1ccccc1C2=O
InChIKey:
AFHWNNJNTNLCQF-UHFFFAOYSA-N
InChI:
InChI=1S/C15H10O3/c1-8-6-11-13(12(16)7-8)15(18)10-5-3-2-4-9(10)14(11)17/h2-7,16H,1H3
Calculated Properties
ALogP:
2.476 lipophilicity
TPSA:
54.37 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
3
Rotatable Bonds:
0
Ring Count:
3 (2 aromatic)
Chiral Centers:
0
Fsp³:
0.0667 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000420
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
Enzyme inhibition inhibition acetylcholinesterase,phytopathogenic fungi 100.0 μM 10.1039/c8ra04865g RSC Advances
Structure enlarged