3-Furoic acid

Details

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Internal ID 8d9c0c2e-996d-48fc-aae7-9ee315e228e8
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acids
IUPAC Name furan-3-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H4O3/c6-5(7)4-1-2-8-3-4/h1-3H,(H,6,7)
InChI Key IHCCAYCGZOLTEU-UHFFFAOYSA-N
Popularity 101 references in papers

Physical and Chemical Properties

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Molecular Formula C5H4O3
Molecular Weight 112.08 g/mol
Exact Mass 112.016043985 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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furan-3-carboxylic acid
488-93-7
3-Furancarboxylic acid
3-carboxyfuran
3-Furanoic acid
MFCD00005350
88A3S7RG98
NSC-349941
UNII-88A3S7RG98
3-Furanoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Furoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9865 98.65%
Caco-2 + 0.7430 74.30%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6052 60.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9565 95.65%
P-glycoprotein inhibitior - 0.9826 98.26%
P-glycoprotein substrate - 0.9942 99.42%
CYP3A4 substrate - 0.8085 80.85%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.9021 90.21%
CYP3A4 inhibition - 0.9760 97.60%
CYP2C9 inhibition - 0.9677 96.77%
CYP2C19 inhibition - 0.9266 92.66%
CYP2D6 inhibition - 0.9543 95.43%
CYP1A2 inhibition - 0.7423 74.23%
CYP2C8 inhibition - 0.9295 92.95%
CYP inhibitory promiscuity - 0.9672 96.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4758 47.58%
Eye corrosion + 0.9548 95.48%
Eye irritation + 0.9968 99.68%
Skin irritation + 0.8740 87.40%
Skin corrosion + 0.5950 59.50%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9262 92.62%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.5606 56.06%
skin sensitisation - 0.7113 71.13%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4530 45.30%
Acute Oral Toxicity (c) III 0.6580 65.80%
Estrogen receptor binding - 0.9592 95.92%
Androgen receptor binding - 0.9310 93.10%
Thyroid receptor binding - 0.8694 86.94%
Glucocorticoid receptor binding - 0.9434 94.34%
Aromatase binding - 0.8616 86.16%
PPAR gamma - 0.8525 85.25%
Honey bee toxicity - 0.9842 98.42%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity + 0.6394 63.94%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.83% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.48% 81.11%
CHEMBL3194 P02766 Transthyretin 83.88% 90.71%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.03% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.64% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.11% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Brachystemma calycinum
Euonymus europaeus
Peristeria elata
Phaseolus vulgaris
Tripterygium wilfordii

Cross-Links

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PubChem 10268
LOTUS LTS0105731
wikiData Q21045227