SCS-C006817

eupenicisirenin G

Pathway: Terpenoids Superclass: Sesquiterpenoids Class: Cyclobisabolane sesquiterpenoids

Chemical Structure

Structure of eupenicisirenin 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

Pestalotiopsis neglecta (SCSIO41403)
South China Sea
DOI: 10.1038/s41429-020-0308-3  · The Journal of Antibiotics

Drug-likeness (Lipinski Ro5)

Molecular Weight
268.4 Da
Threshold ≤ 500
ALogP
1.96
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
3
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H24O4
Molecular Weight:
268.3530 Da
SMILES:
CC(C)(O)[C@H](O)CC[C@@]1(C)[C@@H]2C=C(C(=O)O)CC[C@@H]21
InChIKey:
XXDOOWZTGBCHRY-FUTJPDQTSA-N
InChI:
InChI=1S/C15H24O4/c1-14(2,19)12(16)6-7-15(3)10-5-4-9(13(17)18)8-11(10)15/h8,10-12,16,19H,4-7H2,1-3H3,(H,17,18)/t10-,11+,12+,15+/m0/s1
Calculated Properties
ALogP:
1.956 lipophilicity
TPSA:
77.76 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
3
Rotatable Bonds:
5
Ring Count:
2 (0 aromatic)
Chiral Centers:
4
Fsp³:
0.8000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006817
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Sesquiterpenoids
NPClassifier Class:
Cyclobisabolane 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
Antiviral — Dengue virus All compounds were evaluated for their activities against Dengue virus infectivity by the cell-based cytopathic effect (CPE) assay, however none of them showed obvious activities with 10 μM. 10.1038/s41429-020-0308-3 The Journal of Antibiotics
Anti-inflammatory — COX-2 Compounds 1, 2 and 5–7 were assessed for their COX-2 inhibitory activities using the COX (ovine) inhibitor screening kit with a series of concentrations 10.1038/s41429-020-0308-3 The Journal of Antibiotics
Structure enlarged