SCS-C007693

stachyline K

Pathway: Shikimates and Phenylpropanoids

Chemical Structure

Structure of stachyline 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

Fusarium oxysporum F0888 (NA)
Kingdom Fungi Phylum Ascomycota Class Sordariomycetes Order Hypocreales Family Nectriaceae Genus Fusarium Species Fusarium oxysporum
South China Sea  · 670 m  · 114.1896° E, 20.0859° N
DOI: 10.1002/cbdv.202400118  · Chemistry & Biodiversity

Drug-likeness (Lipinski Ro5)

Molecular Weight
310.3 Da
Threshold ≤ 500
ALogP
1.48
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
6
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C16H22O6
Molecular Weight:
310.3460 Da
SMILES:
COC(=O)Cc1ccc(OC[C@@H](OC(C)=O)C(C)(C)O)cc1
InChIKey:
DIXAPCJDVWYVPG-CQSZACIVSA-N
InChI:
InChI=1S/C16H22O6/c1-11(17)22-14(16(2,3)19)10-21-13-7-5-12(6-8-13)9-15(18)20-4/h5-8,14,19H,9-10H2,1-4H3/t14-/m1/s1
Calculated Properties
ALogP:
1.484 lipophilicity
TPSA:
82.06 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
6
Rotatable Bonds:
7
Ring Count:
1 (1 aromatic)
Chiral Centers:
1
Fsp³:
0.5000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007693
NPClassifier Pathway:
Shikimates and Phenylpropanoids
NPClassifier Superclass:
N/A
NPClassifier Class:
N/A
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
Antibacterial MIC Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeruginosa, Vibrio harveyi, Vibrio alginolyticus, Vibrio parahaemolyticus, Candida albicans > 100.0 μg/mL 10.1002/cbdv.202400118 Chemistry & Biodiversity
Anti-inflammatory — RAW 264.7 macrophage cells Anti–inflammatory activities of compounds 1–12 were tested. Unfortunately, all of isolated compounds were inactive. 10.1002/cbdv.202400118 Chemistry & Biodiversity
Structure enlarged