3-Hydroxy-2,3-dihydrobenzofuran-5-carboxylic acid

Details

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Internal ID bffddd37-6952-4376-b564-74b9303aec69
Taxonomy Organoheterocyclic compounds > Coumarans
IUPAC Name 3-hydroxy-2,3-dihydro-1-benzofuran-5-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H8O4/c10-7-4-13-8-2-1-5(9(11)12)3-6(7)8/h1-3,7,10H,4H2,(H,11,12)
InChI Key WPJOUHBHNOSJMG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O4
Molecular Weight 180.16 g/mol
Exact Mass 180.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.81
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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RefChem:911350
3-Hydroxy-2,3-dihydro-1-benzofuran-5-carboxylic acid
1378713-14-4
SCHEMBL28346970
EN300-222540
3-Hydroxy-2,3-dihydro-1-benzofuran-5-carboxylicacid

2D Structure

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2D Structure of 3-Hydroxy-2,3-dihydrobenzofuran-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 + 0.9924 99.24%
Caco-2 - 0.5979 59.79%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6970 69.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9731 97.31%
OATP1B3 inhibitior + 0.9031 90.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9762 97.62%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9380 93.80%
CYP3A4 substrate - 0.7023 70.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7986 79.86%
CYP3A4 inhibition - 0.9598 95.98%
CYP2C9 inhibition - 0.9205 92.05%
CYP2C19 inhibition - 0.9276 92.76%
CYP2D6 inhibition - 0.9349 93.49%
CYP1A2 inhibition - 0.5258 52.58%
CYP2C8 inhibition - 0.7508 75.08%
CYP inhibitory promiscuity - 0.9126 91.26%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5199 51.99%
Eye corrosion - 0.9481 94.81%
Eye irritation + 0.9849 98.49%
Skin irritation - 0.5341 53.41%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8375 83.75%
Micronuclear + 0.6773 67.73%
Hepatotoxicity - 0.5436 54.36%
skin sensitisation - 0.6285 62.85%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5990 59.90%
Acute Oral Toxicity (c) III 0.5837 58.37%
Estrogen receptor binding - 0.7311 73.11%
Androgen receptor binding - 0.7224 72.24%
Thyroid receptor binding - 0.6710 67.10%
Glucocorticoid receptor binding - 0.6939 69.39%
Aromatase binding - 0.7276 72.76%
PPAR gamma - 0.5997 59.97%
Honey bee toxicity - 0.9455 94.55%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7752 77.52%
Fish aquatic toxicity - 0.4150 41.50%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.60% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.86% 87.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.01% 91.11%
CHEMBL3194 P02766 Transthyretin 84.93% 90.71%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 84.29% 89.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.93% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.45% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.78% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.76% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.54% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.06% 100.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.90% 90.24%
CHEMBL340 P08684 Cytochrome P450 3A4 80.78% 91.19%

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 122199535
LOTUS LTS0199237
wikiData Q77564412