SCS-C007744

talaraculone G

Pathway: Polyketides Superclass: Chromanes Class: Azaphilones

Chemical Structure

Structure of talaraculone 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: 10.1002/cbdv.202500201  · Chemistry & Biodiversity

Drug-likeness (Lipinski Ro5)

Molecular Weight
434.4 Da
Threshold ≤ 500
ALogP
1.12
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
9
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C22H26O9
Molecular Weight:
434.4410 Da
SMILES:
COC(CO)CC1=CC2=CC(=O)C(C)(O)C(OC(=O)c3c(C)cc(O)cc3O)C2CO1
InChIKey:
GCKDHZYNICVWHW-UHFFFAOYSA-N
InChI:
InChI=1S/C22H26O9/c1-11-4-13(24)7-17(25)19(11)21(27)31-20-16-10-30-14(8-15(9-23)29-3)5-12(16)6-18(26)22(20,2)28/h4-7,15-16,20,23-25,28H,8-10H2,1-3H3
Calculated Properties
ALogP:
1.119 lipophilicity
TPSA:
142.75 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
9
Rotatable Bonds:
6
Ring Count:
3 (1 aromatic)
Chiral Centers:
4
Fsp³:
0.4545 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007744
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Chromanes
NPClassifier Class:
Azaphilones
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 51.98–64.78 μM 10.1002/cbdv.202500201 Chemistry & Biodiversity
Anti-inflammatory IC50 nitric oxide production 31.0–39.0 μM 10.1002/cbdv.202500201 Chemistry & Biodiversity
Structure enlarged