1-Benzofuran-5-Carboxylic Acid

Details

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Internal ID 4713e740-c295-41e6-86f0-32f57beae4d1
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 1-benzofuran-5-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H6O3/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-5H,(H,10,11)
InChI Key GTWXSZIQNTUNKR-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O3
Molecular Weight 162.14 g/mol
Exact Mass 162.031694049 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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90721-27-0
benzofuran-5-carboxylic acid
Benzo[b]furan-5-carboxylic acid
MFCD01006742
5-BENZOFURANCARBOXYLIC ACID
Benzofurane-5-carboxylic acid
4ctj
5-benzofuran carboxylic
benzofuran-5-carboxylicacid
SCHEMBL663873
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Benzofuran-5-Carboxylic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8758 87.58%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Plasma membrane 0.4352 43.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9603 96.03%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9258 92.58%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9880 98.80%
CYP3A4 substrate - 0.7820 78.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8815 88.15%
CYP3A4 inhibition - 0.9692 96.92%
CYP2C9 inhibition - 0.9645 96.45%
CYP2C19 inhibition - 0.9405 94.05%
CYP2D6 inhibition - 0.9618 96.18%
CYP1A2 inhibition + 0.5250 52.50%
CYP2C8 inhibition - 0.7825 78.25%
CYP inhibitory promiscuity - 0.9531 95.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8036 80.36%
Carcinogenicity (trinary) Non-required 0.4823 48.23%
Eye corrosion - 0.7662 76.62%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8085 80.85%
Skin corrosion - 0.9489 94.89%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8709 87.09%
Micronuclear + 0.5059 50.59%
Hepatotoxicity + 0.6534 65.34%
skin sensitisation - 0.6048 60.48%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5963 59.63%
Acute Oral Toxicity (c) III 0.8249 82.49%
Estrogen receptor binding - 0.8422 84.22%
Androgen receptor binding - 0.5183 51.83%
Thyroid receptor binding - 0.8256 82.56%
Glucocorticoid receptor binding - 0.7049 70.49%
Aromatase binding - 0.7218 72.18%
PPAR gamma - 0.5470 54.70%
Honey bee toxicity - 0.9624 96.24%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.8552 85.52%

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 93.08% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.42% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.37% 86.33%
CHEMBL1811 P34995 Prostanoid EP1 receptor 88.62% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.13% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 85.93% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.66% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.86% 91.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.14% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.01% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.67% 95.56%
CHEMBL3194 P02766 Transthyretin 80.39% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 595656
LOTUS LTS0073526
wikiData Q72445519