SCS-C007820

herbabysidolide

Pathway: Terpenoids Superclass: Sesquiterpenoids Class: Isolactarane sesquiterpenoids

Chemical Structure

Structure of herbabysidolide
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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

Hexabranchus sanguineus (NA)
South China Sea
DOI: 10.1002/chem.202203858  · Chemistry – A European Journal

Drug-likeness (Lipinski Ro5)

Molecular Weight
234.3 Da
Threshold ≤ 500
ALogP
3.32
Threshold ≤ 5
H-Bond Donors
0
Threshold ≤ 5
H-Bond Acceptors
2
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H22O2
Molecular Weight:
234.3390 Da
SMILES:
CC1=C[C@@H]2C[C@]3(CCOC3=O)C(C)(C)[C@@H]2CC1
InChIKey:
LWKYOCBKCDIMKI-JMSVASOKSA-N
InChI:
InChI=1S/C15H22O2/c1-10-4-5-12-11(8-10)9-15(14(12,2)3)6-7-17-13(15)16/h8,11-12H,4-7,9H2,1-3H3/t11-,12-,15+/m1/s1
Calculated Properties
ALogP:
3.322 lipophilicity
TPSA:
26.30 Ų polar surface area
H-Bond Donors:
0
H-Bond Acceptors:
2
Rotatable Bonds:
0
Ring Count:
3 (0 aromatic)
Chiral Centers:
3
Fsp³:
0.8000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007820
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Sesquiterpenoids
NPClassifier Class:
Isolactarane sesquiterpenoids
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged