SCS-C000509

cochliomycin C

Pathway: Polyketides Superclass: Macrolides Class: Zearalenones

Chemical Structure

Structure of cochliomycin C
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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

Cochliobolus lunatus (gorgonian-derived fungus)
Kingdom Fungi Phylum Ascomycota Class Dothideomycetes Order Pleosporales Family Pleosporaceae Genus Curvularia Species Cochliobolus lunatus
South China Sea
DOI: 10.1016/s0014-2999(00)00834-7  · Eur. J. Pharmacol

Drug-likeness (Lipinski Ro5)

Molecular Weight
398.8 Da
Threshold ≤ 500
ALogP
2.05
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
7
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C19H23ClO7
Molecular Weight:
398.8000 Da
SMILES:
COc1cc(O)c2c(c1Cl)/C=C/C[C@H](O)[C@H](O)[C@H](O)/C=C/C[C@H](C)OC2=O
InChIKey:
ASZQCWYVQBKBBJ-KOAAHNDQSA-N
InChI:
InChI=1S/C19H23ClO7/c1-10-5-3-7-12(21)18(24)13(22)8-4-6-11-16(19(25)27-10)14(23)9-15(26-2)17(11)20/h3-4,6-7,9-10,12-13,18,21-24H,5,8H2,1-2H3/b6-4+,7-3+/t10-,12+,13-,18+/m0/s1
Calculated Properties
ALogP:
2.045 lipophilicity
TPSA:
116.45 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
7
Rotatable Bonds:
1
Ring Count:
2 (1 aromatic)
Chiral Centers:
4
Fsp³:
0.4211 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000509
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Macrolides
NPClassifier Class:
Zearalenones
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged