Artoindonesianin Q

Details

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Internal ID 98532bee-6f98-4a40-bf41-2e7eed141e80
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 3-prenylated flavones
IUPAC Name 2-(2,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3O)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3O)OC)O)C
InChI InChI=1S/C22H22O7/c1-11(2)5-6-13-21(26)20-17(25)7-12(27-3)8-19(20)29-22(13)14-9-16(24)18(28-4)10-15(14)23/h5,7-10,23-25H,6H2,1-4H3
InChI Key YIGFIYUYIAFKOH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H22O7
Molecular Weight 398.40 g/mol
Exact Mass 398.13655304 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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CHEBI:178247
LMPK12110910
2-(2,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-enyl)chromen-4-one

2D Structure

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2D Structure of Artoindonesianin Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.6718 67.18%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7233 72.33%
OATP2B1 inhibitior - 0.5581 55.81%
OATP1B1 inhibitior + 0.8602 86.02%
OATP1B3 inhibitior + 0.8680 86.80%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6573 65.73%
P-glycoprotein inhibitior + 0.7352 73.52%
P-glycoprotein substrate - 0.7171 71.71%
CYP3A4 substrate + 0.5855 58.55%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7963 79.63%
CYP2C9 inhibition + 0.8697 86.97%
CYP2C19 inhibition + 0.9595 95.95%
CYP2D6 inhibition - 0.5753 57.53%
CYP1A2 inhibition + 0.7459 74.59%
CYP2C8 inhibition + 0.6587 65.87%
CYP inhibitory promiscuity + 0.9318 93.18%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6472 64.72%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.7424 74.24%
Skin irritation - 0.7666 76.66%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5866 58.66%
Micronuclear + 0.5500 55.00%
Hepatotoxicity - 0.5415 54.15%
skin sensitisation - 0.8402 84.02%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6910 69.10%
Acute Oral Toxicity (c) III 0.7283 72.83%
Estrogen receptor binding + 0.8803 88.03%
Androgen receptor binding + 0.7755 77.55%
Thyroid receptor binding + 0.5674 56.74%
Glucocorticoid receptor binding + 0.9037 90.37%
Aromatase binding + 0.6927 69.27%
PPAR gamma + 0.8937 89.37%
Honey bee toxicity - 0.8155 81.55%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9885 98.85%

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 98.81% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.30% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.65% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.70% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.82% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.01% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 91.80% 94.73%
CHEMBL3194 P02766 Transthyretin 91.13% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.08% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.13% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.36% 94.45%
CHEMBL4208 P20618 Proteasome component C5 86.11% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.20% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.85% 91.49%
CHEMBL2535 P11166 Glucose transporter 83.55% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.89% 96.09%

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.
Artocarpus integer

Cross-Links

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PubChem 5320428
LOTUS LTS0177836
wikiData Q105348827