Benzofuran

Details

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Internal ID e0bd8592-0c42-4d1e-b22b-1ecae832bc1c
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 1-benzofuran
SMILES (Canonical) C1=CC=C2C(=C1)C=CO2
SMILES (Isomeric) C1=CC=C2C(=C1)C=CO2
InChI InChI=1S/C8H6O/c1-2-4-8-7(3-1)5-6-9-8/h1-6H
InChI Key IANQTJSKSUMEQM-UHFFFAOYSA-N
Popularity 3,559 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O
Molecular Weight 118.13 g/mol
Exact Mass 118.041864811 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,3-Benzofuran
271-89-6
Coumarone
1-Benzofuran
Benzo[b]furan
Cumarone
Benzofurfuran
Benzo(b)furan
Coumaron
1-Oxindene
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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9628 96.28%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.6154 61.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9460 94.60%
OATP1B3 inhibitior + 0.9695 96.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9392 93.92%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.9938 99.38%
CYP3A4 substrate - 0.7784 77.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6725 67.25%
CYP3A4 inhibition - 0.9711 97.11%
CYP2C9 inhibition - 0.9453 94.53%
CYP2C19 inhibition - 0.5512 55.12%
CYP2D6 inhibition - 0.8558 85.58%
CYP1A2 inhibition + 0.7156 71.56%
CYP2C8 inhibition - 0.8815 88.15%
CYP inhibitory promiscuity - 0.5839 58.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7436 74.36%
Carcinogenicity (trinary) Warning 0.5851 58.51%
Eye corrosion + 0.5422 54.22%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8898 88.98%
Skin corrosion - 0.9504 95.04%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7812 78.12%
Micronuclear - 0.5259 52.59%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.6957 69.57%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6918 69.18%
Acute Oral Toxicity (c) III 0.7670 76.70%
Estrogen receptor binding - 0.8279 82.79%
Androgen receptor binding - 0.6529 65.29%
Thyroid receptor binding - 0.8465 84.65%
Glucocorticoid receptor binding - 0.8611 86.11%
Aromatase binding - 0.8037 80.37%
PPAR gamma - 0.8714 87.14%
Honey bee toxicity - 0.9098 90.98%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity - 0.3716 37.16%

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 92.40% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.74% 95.56%
CHEMBL240 Q12809 HERG 81.72% 89.76%
CHEMBL3959 P16083 Quinone reductase 2 80.12% 89.49%

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.
Curcuma aromatica
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria
Ephedra sinica
Sarcandra glabra
Trichosanthes kirilowii
Vitex agnus-castus

Cross-Links

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PubChem 9223
NPASS NPC206007
LOTUS LTS0118545
wikiData Q410089