SCS-C006877
sarcoehrenolide G
Pathway: Terpenoids
Superclass: Diterpenoids
Class: Cembrane diterpenoids
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
Sarcophyton ehrenbergi
(soft coral)
Original source name: Sarcophyton ehrenbergi Marenzeller (Sarcophytidae)
Kingdom
Metazoa
Phylum
Cnidaria
Class
Anthozoa
Order
Malacalcyonacea
Family
Alcyoniidae
Genus
Sarcophyton
Species
Sarcophyton ehrenbergi
South China Sea
· -20 m
· 20°54′-21°10′N, 109°00-109°15′E
DOI:
10.1016/j.phytochem.2022.113549
· Phytochemistry
Drug-likeness (Lipinski Ro5)
Molecular Weight
346.5 Da
Threshold ≤ 500
ALogP
3.87
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate
Chemical Properties
Molecular Formula:
C21H30O4
Molecular Weight:
346.4670 Da
SMILES:
CO[C@]1(C)/C=C/CC2=C[C@H](C/C(CO)=C\C=C(\C(C)C)CC1)OC2=O
InChIKey:
RCMUVPPYDPPZRW-ICUSNOPOSA-N
InChI:
InChI=1S/C21H30O4/c1-15(2)17-8-7-16(14-22)12-19-13-18(20(23)25-19)6-5-10-21(3,24-4)11-9-17/h5,7-8,10,13,15,19,22H,6,9,11-12,14H2,1-4H3/b10-5+,16-7+,17-8+/t19-,21+/m0/s1
Calculated Properties
ALogP:
3.875 lipophilicity
TPSA:
55.76 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
4
Rotatable Bonds:
3
Ring Count:
2
(0 aromatic)
Chiral Centers:
2
Fsp³:
0.5714 fraction sp³ carbon
Database Information
Compound ID:
SCS-C006877
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Diterpenoids
NPClassifier Class:
Cembrane diterpenoids
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 |
|---|---|---|---|---|
| Anti-inflammatory | inhibition rate | LPS-induced TNF-α production | < 50.0 % | 10.1016/j.phytochem.2022.113549 Phytochemistry |