SCS-C008199
neocucurbol C
Pathway: Terpenoids
Chemical Structure
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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.
Source Information
Neocucurbitaria unguis-hominis
(NA)
Kingdom
Fungi
Phylum
Ascomycota
Class
Dothideomycetes
Order
Pleosporales
Family
Cucurbitariaceae
Genus
Neocucurbitaria
Species
Neocucurbitaria unguis-hominis
South China Sea
· 3698 m
· 115°21.569' E, 18°58.39' N
DOI:
10.1021/acs.jnatprod.2c00249
· Journal of Natural Products
Drug-likeness (Lipinski Ro5)
Molecular Weight
332.4 Da
Threshold ≤ 500
ALogP
2.23
Threshold ≤ 5
H-Bond Donors
2
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate
Chemical Properties
Molecular Formula:
C20H28O4
Molecular Weight:
332.4400 Da
SMILES:
CC1=CC[C@@H]2[C@@]3(C)CC[C@@]4(C)[C@H](C)CC(=O)[C@H]5[C@@]2(O[C@@H]3[C@]54O)[C@H]1O
InChIKey:
JSWSSIITSSRKRV-OUZKRQETSA-N
InChI:
InChI=1S/C20H28O4/c1-10-5-6-13-17(3)7-8-18(4)11(2)9-12(21)14-19(13,15(10)22)24-16(17)20(14,18)23/h5,11,13-16,22-23H,6-9H2,1-4H3/t11-,13-,14+,15+,16+,17-,18+,19-,20-/m1/s1
Calculated Properties
ALogP:
2.227 lipophilicity
TPSA:
66.76 Ų polar surface area
H-Bond Donors:
2
H-Bond Acceptors:
4
Rotatable Bonds:
0
Ring Count:
5
(0 aromatic)
Chiral Centers:
9
Fsp³:
0.8500 fraction sp³ carbon
Database Information
Compound ID:
SCS-C008199
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
N/A
NPClassifier Class:
N/A
Glycoside:
No
NPClassifier Status:
Classified
External Links:
General chemistry
Natural product databases
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 |
|---|---|---|---|---|
| Antitumor | IC50 | human cancer cell lines SF-268, MCF-7, HepG-2, A549 | > 10.0 μM | 10.1021/acs.jnatprod.2c00249 Journal of Natural Products |
| Antibacterial | — | Escherichia coli, Staphylococcus aureus | none of the tested compounds showed antimicrobial activity. | 10.1021/acs.jnatprod.2c00249 Journal of Natural Products |