SCS-C007698

2-(4-((3-methylbut-2-en-1-yl)oxy)phenyl) acetic acid

Chemical Structure

Structure of 2-(4-((3-methylbut-2-en-1-yl)oxy)phenyl) acetic acid
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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

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
220.3 Da
Threshold ≤ 500
ALogP
2.66
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
2
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C13H16O3
Molecular Weight:
220.2680 Da
SMILES:
CC(C)=CCOc1ccc(CC(=O)O)cc1
InChIKey:
YFTIKQOPFVOWHB-UHFFFAOYSA-N
InChI:
InChI=1S/C13H16O3/c1-10(2)7-8-16-12-5-3-11(4-6-12)9-13(14)15/h3-7H,8-9H2,1-2H3,(H,14,15)
Calculated Properties
ALogP:
2.659 lipophilicity
TPSA:
46.53 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
2
Rotatable Bonds:
5
Ring Count:
1 (1 aromatic)
Chiral Centers:
0
Fsp³:
0.3077 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007698
NPClassifier Pathway:
N/A
NPClassifier Superclass:
N/A
NPClassifier Class:
N/A
Glycoside:
No
NPClassifier Status:
No classification
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