SCS-C000359

libertalide C

Pathway: Polyketides Superclass: Cyclic polyketides Class: Monacolins and Monacolin derivatives

Chemical Structure

Structure of libertalide 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

Libertasomyces sp. (NA)
Kingdom Fungi Phylum Ascomycota Class Dothideomycetes Order Pleosporales Family NA Genus Libertasomyces Species NA
South China Sea
DOI: 10.1021/acs.jnatprod.7b00463  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
252.3 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:
252.3500 Da
SMILES:
CC(=O)[C@]1(C)[C@H]2CC[C@@](C)(O)C[C@@H]2C=C[C@@]1(C)O
InChIKey:
YAYPYLHOLGSFLY-VQJWOFKYSA-N
InChI:
InChI=1S/C15H24O3/c1-10(16)15(4)12-6-7-13(2,17)9-11(12)5-8-14(15,3)18/h5,8,11-12,17-18H,6-7,9H2,1-4H3/t11-,12-,13+,14+,15+/m0/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:
5
Fsp³:
0.8000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C000359
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Cyclic polyketides
NPClassifier Class:
Monacolins and Monacolin derivatives
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
Immunomodulatory / Anti-allergic — — — Structured numeric value is not available in this record; see the primary reference. 10.1021/acs.jnatprod.7b00463 Journal of Natural Products
Structure enlarged