2-(3-Methyl-2-butenyl)-3,6-dimethylbenzofuran-5-ol

Details

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Internal ID 8429927e-694e-4c79-8c26-e1b831e9a89f
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 3,6-dimethyl-2-(3-methylbut-2-enyl)-1-benzofuran-5-ol
SMILES (Canonical) CC1=CC2=C(C=C1O)C(=C(O2)CC=C(C)C)C
SMILES (Isomeric) CC1=CC2=C(C=C1O)C(=C(O2)CC=C(C)C)C
InChI InChI=1S/C15H18O2/c1-9(2)5-6-14-11(4)12-8-13(16)10(3)7-15(12)17-14/h5,7-8,16H,6H2,1-4H3
InChI Key BVWSXPXKZJKORS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O2
Molecular Weight 230.30 g/mol
Exact Mass 230.130679813 g/mol
Topological Polar Surface Area (TPSA) 33.40 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3-Methyl-2-butenyl)-3,6-dimethylbenzofuran-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 + 0.9228 92.28%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6708 67.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8975 89.75%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8994 89.94%
P-glycoprotein substrate - 0.8290 82.90%
CYP3A4 substrate - 0.5679 56.79%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate + 0.3752 37.52%
CYP3A4 inhibition - 0.7792 77.92%
CYP2C9 inhibition - 0.6550 65.50%
CYP2C19 inhibition + 0.5792 57.92%
CYP2D6 inhibition - 0.8612 86.12%
CYP1A2 inhibition + 0.8733 87.33%
CYP2C8 inhibition - 0.7567 75.67%
CYP inhibitory promiscuity + 0.8643 86.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8608 86.08%
Carcinogenicity (trinary) Non-required 0.4874 48.74%
Eye corrosion - 0.9794 97.94%
Eye irritation + 0.9272 92.72%
Skin irritation - 0.6183 61.83%
Skin corrosion - 0.8892 88.92%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4407 44.07%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.6314 63.14%
skin sensitisation + 0.7114 71.14%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8155 81.55%
Acute Oral Toxicity (c) III 0.6860 68.60%
Estrogen receptor binding + 0.6421 64.21%
Androgen receptor binding + 0.6112 61.12%
Thyroid receptor binding + 0.5862 58.62%
Glucocorticoid receptor binding + 0.6192 61.92%
Aromatase binding + 0.6127 61.27%
PPAR gamma + 0.6831 68.31%
Honey bee toxicity - 0.9347 93.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9768 97.68%

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 97.19% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.73% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 92.52% 91.49%
CHEMBL2581 P07339 Cathepsin D 87.39% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.04% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.06% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.08% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.87% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.13% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.44% 96.95%

Cross-Links

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PubChem 10398970
NPASS NPC25769
LOTUS LTS0050191
wikiData Q104946959