Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Within Vinony's link graph, fusaric acid is referenced by 197 other articles, and connects out to L-tyrosine, 3-methoxy-4-hydroxyphenylglycol and 3,4-dihydroxyphenylacetic acid.
It sits within the topics Butyl compounds, Carboxylic acids and Chembox having GHS data.
Its subject is documented across 6 Wikipedia language editions.
Chemical data
- Formula
- C10H13NO2
- Molecular weight
- 179.22 g/mol
- IUPAC name
- 5-butylpyridine-2-carboxylic acid
- SMILES
- CCCCC1=CN=C(C=C1)C(=O)O
- InChIKey
- DGMPVYSXXIOGJY-UHFFFAOYSA-N
- XLogP
- 2.6
- Polar surface area
- 50.2 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
568 papers- Fusaric acid-evoked oxidative stress affects plant defence system by inducing biochemical changes at subcellular level.Plant cell reports · 2023
- Fusaric acid inhibits cell proliferation and downregulates expressions of toll-like receptors pathway genes in Ishikawa endometrial cancer cells.European review for medical and pharmacological sciences · 2023
- Pharmacological activities of fusaric acid (5-butylpicolinic acid).Life sciences · 1999
- Fusaric acid and analogues as Gram-negative bacterial quorum sensing inhibitors.European journal of medicinal chemistry · 2017
- Fusaric acid and pathogenic interactions of corn and non-corn isolates of Fusarium moniliforme, a nonobligate pathogen of corn.Advances in experimental medicine and biology · 1996
via PubMed
Wikidata facts
- Subclass of
- carboxylic acid
- Mass
- 179.095
Show 3 more facts
- Commons category
- Fusaric acid
- chemical formula
- C₁₀H₁₃NO₂
- canonical SMILES
- CCCCC1=CN=C(C=C1)C(=O)O
via Wikidata · CC0
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