Benzofuran-5-ol

Details

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Internal ID 52babbf9-9c49-4ba8-b042-572b7d38a107
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 1-benzofuran-5-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H6O2/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,9H
InChI Key IZFOPMSVNDORMZ-UHFFFAOYSA-N
Popularity 50 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O2
Molecular Weight 134.13 g/mol
Exact Mass 134.036779430 g/mol
Topological Polar Surface Area (TPSA) 33.40 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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13196-10-6
1-benzofuran-5-ol
DTXSID00470002
RefChem:1078899
DTXCID00420820
5-BENZOFURANOL
5-Hydroxybenzofuran
MFCD10699412
5-Hydroxybenzo[b]furan
CHEMBL349283
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzofuran-5-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9558 95.58%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4090 40.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8965 89.65%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9600 96.00%
P-glycoprotein inhibitior - 0.9739 97.39%
P-glycoprotein substrate - 0.9763 97.63%
CYP3A4 substrate - 0.7310 73.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6705 67.05%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.7647 76.47%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition + 0.8380 83.80%
CYP2C8 inhibition - 0.6694 66.94%
CYP inhibitory promiscuity - 0.7555 75.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8162 81.62%
Carcinogenicity (trinary) Warning 0.6066 60.66%
Eye corrosion - 0.7795 77.95%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8154 81.54%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7066 70.66%
Micronuclear + 0.5759 57.59%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.6722 67.22%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6054 60.54%
Acute Oral Toxicity (c) III 0.7435 74.35%
Estrogen receptor binding - 0.6148 61.48%
Androgen receptor binding + 0.6686 66.86%
Thyroid receptor binding - 0.7577 75.77%
Glucocorticoid receptor binding - 0.8652 86.52%
Aromatase binding - 0.7087 70.87%
PPAR gamma - 0.6022 60.22%
Honey bee toxicity - 0.9356 93.56%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.6802 68.02%

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 96.13% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 86.73% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.92% 99.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.30% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.86% 86.33%
CHEMBL2581 P07339 Cathepsin D 80.81% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.30% 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.
There are no matching plants.

Cross-Links

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PubChem 11651159
LOTUS LTS0008076
wikiData Q82297953