6-Hydroxybenzofuran-5-carbimidic acid

Details

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Internal ID 5a5ab624-31af-4df2-9263-e93aa888d0cb
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives
IUPAC Name 6-hydroxy-1-benzofuran-5-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H7NO3/c10-9(12)6-3-5-1-2-13-8(5)4-7(6)11/h1-4,11H,(H2,10,12)
InChI Key RDEKEWVOOJBTET-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7NO3
Molecular Weight 177.16 g/mol
Exact Mass 177.042593085 g/mol
Topological Polar Surface Area (TPSA) 76.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.24
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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64758-63-0
CHEMBL3634196

2D Structure

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2D Structure of 6-Hydroxybenzofuran-5-carbimidic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8925 89.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5283 52.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9733 97.33%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9282 92.82%
P-glycoprotein inhibitior - 0.9673 96.73%
P-glycoprotein substrate - 0.9566 95.66%
CYP3A4 substrate - 0.7279 72.79%
CYP2C9 substrate - 0.6106 61.06%
CYP2D6 substrate - 0.8809 88.09%
CYP3A4 inhibition - 0.9046 90.46%
CYP2C9 inhibition - 0.9315 93.15%
CYP2C19 inhibition - 0.8088 80.88%
CYP2D6 inhibition - 0.8433 84.33%
CYP1A2 inhibition + 0.5674 56.74%
CYP2C8 inhibition - 0.8366 83.66%
CYP inhibitory promiscuity - 0.8184 81.84%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5621 56.21%
Eye corrosion - 0.9926 99.26%
Eye irritation + 0.9456 94.56%
Skin irritation - 0.7762 77.62%
Skin corrosion - 0.9735 97.35%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7568 75.68%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7926 79.26%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6133 61.33%
Acute Oral Toxicity (c) III 0.5864 58.64%
Estrogen receptor binding + 0.5307 53.07%
Androgen receptor binding - 0.5088 50.88%
Thyroid receptor binding - 0.5219 52.19%
Glucocorticoid receptor binding + 0.6672 66.72%
Aromatase binding + 0.6256 62.56%
PPAR gamma + 0.7037 70.37%
Honey bee toxicity - 0.9444 94.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.13% 91.11%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 86.77% 83.10%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.07% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.83% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.00% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.64% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.35% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.06% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.28% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.28% 90.71%

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.
Tephrosia purpurea

Cross-Links

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PubChem 121227075
LOTUS LTS0120386
wikiData Q105234170