SCS-C006011

Eurothiocin G

Pathway: Polyketides Superclass: Aromatic polyketides Class: Simple aromatic polyketides

Chemical Structure

Structure of Eurothiocin G
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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

Talaromyces indigoticus FS688 (NA)
South China Sea  · 2372 m  · 118°19.692′ N, 20°38.982′ E
DOI: 10.3390/md20010033  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
284.4 Da
Threshold ≤ 500
ALogP
2.61
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C14H20O4S
Molecular Weight:
284.3770 Da
SMILES:
CSC(=O)c1c(C)cc(O)c(CCC(C)(C)O)c1O
InChIKey:
DOYCZFNSXBXAGS-UHFFFAOYSA-N
InChI:
InChI=1S/C14H20O4S/c1-8-7-10(15)9(5-6-14(2,3)18)12(16)11(8)13(17)19-4/h7,15-16,18H,5-6H2,1-4H3
Calculated Properties
ALogP:
2.613 lipophilicity
TPSA:
77.76 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
5
Rotatable Bonds:
4
Ring Count:
1 (1 aromatic)
Chiral Centers:
0
Fsp³:
0.5000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006011
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Aromatic polyketides
NPClassifier Class:
Simple aromatic polyketides
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 IC50 α-glucosidase 72.1 μM 10.3390/md20010033 Marine Drugs
Structure enlarged