SCS-C001415

3-Ethyl-6-hydroxyphthalide

Pathway: Polyketides Superclass: Cyclic polyketides Class: Phthalide derivatives

Chemical Structure

Structure of 3-Ethyl-6-hydroxyphthalide
Loading 3D structure...
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

Cochliobolus lunatus SCSIO 41401 (gorgonian-derived fungus)
Original source name: Cochliobolus lunatus SCSIO41401
Kingdom Fungi Phylum Ascomycota Class Dothideomycetes Order Pleosporales Family Pleosporaceae Genus Curvularia Species Cochliobolus lunatus
Yongxing Island
DOI: 10.1021/acs.jnatprod.8b00015  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
178.1 Da
Threshold ≤ 500
ALogP
2.01
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:
C10H10O3
Molecular Weight:
178.0681 Da
SMILES:
CC[C@@H]1OC(=O)c2cc(O)ccc21
InChIKey:
AIHVXKPMAWGFLZ-VIFPVBQESA-N
InChI:
InChI=1S/C10H10O3/c1-2-9-7-4-3-6(11)5-8(7)10(12)13-9/h3-5,9,11H,2H2,1H3/t9-/m0/s1
Calculated Properties
ALogP:
2.014 lipophilicity
TPSA:
46.53 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
3
Rotatable Bonds:
1
Ring Count:
2 (1 aromatic)
Chiral Centers:
1
Fsp³:
0.3000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C001415
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Cyclic polyketides
NPClassifier Class:
Phthalide derivatives
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
Antitumor — ACHN,786-O,OS-RC-2,HepG-2,SGC7901 > 50.0 μM 10.1021/acs.jnatprod.8b00015 Journal of Natural Products
Structure enlarged