SCS-C006010

Eurothiocin F

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

Chemical Structure

Structure of Eurothiocin F
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

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
282.4 Da
Threshold ≤ 500
ALogP
2.39
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:
C14H18O4S
Molecular Weight:
282.3610 Da
SMILES:
CSC(=O)c1c(C)cc(O)c(C/C=C(\C)CO)c1O
InChIKey:
OGNNVQGJWWISTQ-XBXARRHUSA-N
InChI:
InChI=1S/C14H18O4S/c1-8(7-15)4-5-10-11(16)6-9(2)12(13(10)17)14(18)19-3/h4,6,15-17H,5,7H2,1-3H3/b8-4+
Calculated Properties
ALogP:
2.390 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:
0.3571 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006010
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 33.6 μM 10.3390/md20010033 Marine Drugs
Structure enlarged