5-Methoxyfuro[2,3-g][3]benzoxepin

Details

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Internal ID a7d7a726-3d66-4f24-affa-614769de361d
Taxonomy Organoheterocyclic compounds > Benzoxepines
IUPAC Name 2-(5-methoxyfuro[3,2-i][3]benzoxepin-2-yl)propan-2-ol
SMILES (Canonical) CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O
SMILES (Isomeric) CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O
InChI InChI=1S/C16H16O4/c1-16(2,17)14-9-10-8-13(18-3)11-4-6-19-7-5-12(11)15(10)20-14/h4-9,17H,1-3H3
InChI Key KXZSEWYHQCKWLI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O4
Molecular Weight 272.29 g/mol
Exact Mass 272.10485899 g/mol
Topological Polar Surface Area (TPSA) 51.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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5-methoxyfuro[2,3-g][3]benzoxepin
263241-09-4
CHEMBL501403
2-(5-methoxyfuro[3,2-i][3]benzoxepin-2-yl)propan-2-ol
BDBM50269162
AKOS040761598
2-[5-Methoxy-furo[2,3-g][3]benzoxepin-2-yl]-2-propanol

2D Structure

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2D Structure of 5-Methoxyfuro[2,3-g][3]benzoxepin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.6459 64.59%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6708 67.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9033 90.33%
OATP1B3 inhibitior + 0.9226 92.26%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6332 63.32%
P-glycoprotein inhibitior - 0.6985 69.85%
P-glycoprotein substrate - 0.7731 77.31%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7476 74.76%
CYP3A4 inhibition + 0.6699 66.99%
CYP2C9 inhibition - 0.7812 78.12%
CYP2C19 inhibition - 0.5293 52.93%
CYP2D6 inhibition - 0.6801 68.01%
CYP1A2 inhibition + 0.5287 52.87%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.5568 55.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8926 89.26%
Carcinogenicity (trinary) Danger 0.4010 40.10%
Eye corrosion - 0.9800 98.00%
Eye irritation + 0.6101 61.01%
Skin irritation - 0.7414 74.14%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3619 36.19%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5336 53.36%
skin sensitisation - 0.7313 73.13%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.4497 44.97%
Acute Oral Toxicity (c) III 0.5664 56.64%
Estrogen receptor binding + 0.9451 94.51%
Androgen receptor binding + 0.8143 81.43%
Thyroid receptor binding + 0.7528 75.28%
Glucocorticoid receptor binding + 0.8142 81.42%
Aromatase binding + 0.9186 91.86%
PPAR gamma + 0.8820 88.20%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9286 92.86%

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 95.32% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.77% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.59% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 88.14% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.81% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.88% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.83% 85.14%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.22% 100.00%

Cross-Links

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PubChem 10084612
NPASS NPC84721
ChEMBL CHEMBL501403
LOTUS LTS0068640
wikiData Q105147613