Isoelliptol

Details

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Internal ID 3432a6dc-2ee1-4094-a498-fbaa6a19a3d5
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 4-O-methylisoflavones
IUPAC Name 6-(2,4,5-trimethoxyphenyl)furo[3,2-g]chromen-5-one
SMILES (Canonical) COC1=CC(=C(C=C1C2=COC3=C(C2=O)C=C4C=COC4=C3)OC)OC
SMILES (Isomeric) COC1=CC(=C(C=C1C2=COC3=C(C2=O)C=C4C=COC4=C3)OC)OC
InChI InChI=1S/C20H16O6/c1-22-16-9-19(24-3)18(23-2)7-12(16)14-10-26-17-8-15-11(4-5-25-15)6-13(17)20(14)21/h4-10H,1-3H3
InChI Key VHLZJIBDJSOIAT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H16O6
Molecular Weight 352.30 g/mol
Exact Mass 352.09468823 g/mol
Topological Polar Surface Area (TPSA) 67.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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CHEMBL481251

2D Structure

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2D Structure of Isoelliptol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8669 86.69%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7702 77.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9363 93.63%
OATP1B3 inhibitior + 0.9776 97.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7624 76.24%
P-glycoprotein inhibitior + 0.9516 95.16%
P-glycoprotein substrate - 0.7782 77.82%
CYP3A4 substrate + 0.5369 53.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.8093 80.93%
CYP2C9 inhibition - 0.6172 61.72%
CYP2C19 inhibition + 0.9351 93.51%
CYP2D6 inhibition - 0.6757 67.57%
CYP1A2 inhibition + 0.9233 92.33%
CYP2C8 inhibition - 0.6349 63.49%
CYP inhibitory promiscuity + 0.8904 89.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.3568 35.68%
Eye corrosion - 0.9809 98.09%
Eye irritation - 0.6636 66.36%
Skin irritation - 0.7726 77.26%
Skin corrosion - 0.9797 97.97%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7509 75.09%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8748 87.48%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5696 56.96%
Acute Oral Toxicity (c) II 0.5984 59.84%
Estrogen receptor binding + 0.8630 86.30%
Androgen receptor binding + 0.7728 77.28%
Thyroid receptor binding + 0.6747 67.47%
Glucocorticoid receptor binding + 0.8717 87.17%
Aromatase binding - 0.5306 53.06%
PPAR gamma + 0.7508 75.08%
Honey bee toxicity - 0.8343 83.43%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9248 92.48%

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
CHEMBL2581 P07339 Cathepsin D 94.66% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.51% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.09% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.99% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.46% 94.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 89.15% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.75% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.33% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 85.81% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.37% 89.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 83.41% 92.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.25% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.75% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.00% 85.14%

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.
Neorautanenia mitis

Cross-Links

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PubChem 44575275
NPASS NPC65846
LOTUS LTS0119110
wikiData Q105286488