SCS-C005849

Eutypelide C

Pathway: Terpenoids Superclass: Sesquiterpenoids Class: Eudesmane sesquiterpenoids

Chemical Structure

Structure of Eutypelide 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

Eutypella sp. F0219 (NA)
Kingdom Fungi Phylum Ascomycota Class Sordariomycetes Order Xylariales Family Diatrypaceae Genus Eutypella Species NA
South China Sea  · -75m  · 114.6609°E, 21.5942°N
DOI: 10.1016/j.phytochem.2024.114121  · Phytochemistry

Drug-likeness (Lipinski Ro5)

Molecular Weight
252.4 Da
Threshold ≤ 500
ALogP
2.07
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
3
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H24O3
Molecular Weight:
252.3540 Da
SMILES:
CC1=CC(=O)C[C@]2(C)[C@@H]1C[C@@H](C(C)(C)O)C[C@@H]2O
InChIKey:
SXOPNNIVMZZHBF-IKVITTDRSA-N
InChI:
InChI=1S/C15H24O3/c1-9-5-11(16)8-15(4)12(9)6-10(7-13(15)17)14(2,3)18/h5,10,12-13,17-18H,6-8H2,1-4H3/t10-,12-,13+,15-/m1/s1
Calculated Properties
ALogP:
2.070 lipophilicity
TPSA:
57.53 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
3
Rotatable Bonds:
1
Ring Count:
2 (0 aromatic)
Chiral Centers:
4
Fsp³:
0.8000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C005849
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Sesquiterpenoids
NPClassifier Class:
Eudesmane sesquiterpenoids
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
Anti-inflammatory inhibition NO production inhibition inhibition in LPS-stimulated BV2 microglia) 10.1016/j.phytochem.2024.114121 Phytochemistry
Structure enlarged