Dibenzofuran

Details

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Internal ID 00c4acb7-d85b-40e0-a675-8959648a8240
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name dibenzofuran
SMILES (Canonical) C1=CC=C2C(=C1)C3=CC=CC=C3O2
SMILES (Isomeric) C1=CC=C2C(=C1)C3=CC=CC=C3O2
InChI InChI=1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H
InChI Key TXCDCPKCNAJMEE-UHFFFAOYSA-N
Popularity 5,718 references in papers

Physical and Chemical Properties

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Molecular Formula C12H8O
Molecular Weight 168.19 g/mol
Exact Mass 168.057514874 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Dibenzo[b,d]furan
132-64-9
diphenylene oxide
Dibenzofurans
2,2'-Biphenylene oxide
2,2'-Biphenylylene oxide
Dibenzo(b,d)furan
Dibenzofuran-D8
Dibenzol(b,d)furan
dibenzofurane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dibenzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8458 84.58%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.5409 54.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7536 75.36%
P-glycoprotein inhibitior - 0.9392 93.92%
P-glycoprotein substrate - 0.9864 98.64%
CYP3A4 substrate - 0.7204 72.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6725 67.25%
CYP3A4 inhibition - 0.9265 92.65%
CYP2C9 inhibition - 0.8354 83.54%
CYP2C19 inhibition + 0.7963 79.63%
CYP2D6 inhibition - 0.7436 74.36%
CYP1A2 inhibition + 0.8626 86.26%
CYP2C8 inhibition - 0.8711 87.11%
CYP inhibitory promiscuity + 0.7498 74.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Warning 0.4637 46.37%
Eye corrosion - 0.7591 75.91%
Eye irritation + 0.9968 99.68%
Skin irritation + 0.8143 81.43%
Skin corrosion - 0.9689 96.89%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7178 71.78%
Micronuclear + 0.5042 50.42%
Hepatotoxicity + 0.8698 86.98%
skin sensitisation + 0.6501 65.01%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6173 61.73%
Acute Oral Toxicity (c) III 0.7328 73.28%
Estrogen receptor binding + 0.7713 77.13%
Androgen receptor binding + 0.5885 58.85%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5397 53.97%
Aromatase binding + 0.6092 60.92%
PPAR gamma + 0.5361 53.61%
Honey bee toxicity - 0.9115 91.15%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.7925 79.25%

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 93.94% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.08% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.50% 94.73%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.43% 94.23%

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.
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Angelica acutiloba
Angelica gigas
Angelica sinensis
Artemisia monosperma
Cornus officinalis

Cross-Links

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PubChem 568
NPASS NPC246214
LOTUS LTS0076708
wikiData Q419513