Ambonone

Details

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Internal ID 6f42a4b0-b320-4a7b-ab86-a587dfa04198
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids
IUPAC Name 6-(2,4,5-trimethoxyphenyl)-6,7-dihydrofuro[3,2-g]chromen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O6/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/h4-9,14H,10H2,1-3H3
InChI Key JEBAYRCLJJUGFS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O6
Molecular Weight 354.40 g/mol
Exact Mass 354.11033829 g/mol
Topological Polar Surface Area (TPSA) 67.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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LMPK12050456

2D Structure

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2D Structure of Ambonone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9379 93.79%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8015 80.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8643 86.43%
P-glycoprotein inhibitior + 0.8447 84.47%
P-glycoprotein substrate - 0.7169 71.69%
CYP3A4 substrate + 0.5414 54.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7524 75.24%
CYP3A4 inhibition + 0.7696 76.96%
CYP2C9 inhibition + 0.7334 73.34%
CYP2C19 inhibition + 0.9278 92.78%
CYP2D6 inhibition - 0.7508 75.08%
CYP1A2 inhibition + 0.8152 81.52%
CYP2C8 inhibition - 0.5937 59.37%
CYP inhibitory promiscuity + 0.8945 89.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5168 51.68%
Eye corrosion - 0.9813 98.13%
Eye irritation - 0.7813 78.13%
Skin irritation - 0.8083 80.83%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7554 75.54%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8103 81.03%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.5847 58.47%
Acute Oral Toxicity (c) III 0.5461 54.61%
Estrogen receptor binding + 0.8842 88.42%
Androgen receptor binding + 0.7658 76.58%
Thyroid receptor binding + 0.6351 63.51%
Glucocorticoid receptor binding + 0.8611 86.11%
Aromatase binding - 0.7609 76.09%
PPAR gamma + 0.6872 68.72%
Honey bee toxicity - 0.7815 78.15%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9144 91.44%

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 95.65% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.54% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.05% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.47% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.00% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.85% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.72% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.56% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.40% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.84% 89.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.07% 96.09%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 83.66% 82.67%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.07% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.90% 92.94%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 82.87% 92.38%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.40% 89.62%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.19% 94.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.09% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.95% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.86% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.96% 96.00%

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.
There are no matching plants.

Cross-Links

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PubChem 44257378
LOTUS LTS0170909
wikiData Q105125921