SCS-C002079

zosteropenilline K

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

Chemical Structure

Structure of zosteropenilline K
Loading 3D structure...
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

Penicillium thomii (brown alga)
Kingdom Fungi Phylum Ascomycota Class Eurotiomycetes Order Eurotiales Family Aspergillaceae Genus Penicillium Species Penicillium thomii
South China Sea
DOI: 10.3390/md15020046  · Marine Drugs

Drug-likeness (Lipinski Ro5)

Molecular Weight
282.3 Da
Threshold ≤ 500
ALogP
0.22
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
5
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C15H22O5
Molecular Weight:
282.3300 Da
SMILES:
C[C@@]1(O)C(=O)C=C2C[C@@H](CO)CC[C@@H]2[C@H]1C(=O)CCO
InChIKey:
ZVVBHCPWACWQFB-LHAJWOIZSA-N
InChI:
InChI=1S/C15H22O5/c1-15(20)13(19)7-10-6-9(8-17)2-3-11(10)14(15)12(18)4-5-16/h7,9,11,14,16-17,20H,2-6,8H2,1H3/t9-,11-,14-,15+/m0/s1
Calculated Properties
ALogP:
0.223 lipophilicity
TPSA:
94.83 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
5
Rotatable Bonds:
4
Ring Count:
2 (0 aromatic)
Chiral Centers:
4
Fsp³:
0.7333 fraction sp³ carbon

Database Information

Compound ID:
SCS-C002079
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
Antitumor inhibition PC-3 cells inhibition 10.3390/md15020046 Marine Drugs
Structure enlarged