Artonin U

Details

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Internal ID 6b25eb95-598a-41aa-840a-6daa21678519
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)OC)C
InChI InChI=1S/C21H20O5/c1-12(2)4-9-15-19(25-3)11-17(24)20-16(23)10-18(26-21(15)20)13-5-7-14(22)8-6-13/h4-8,10-11,22,24H,9H2,1-3H3
InChI Key BSZYNZDGUZYMDL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20O5
Molecular Weight 352.40 g/mol
Exact Mass 352.13107373 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEBI:175517
DTXSID201124932
LMPK12111015
4',5-Dihydroxy-7-methoxy-8-prenylflavone
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one
5-Hydroxy-2-(4-Hydroxyphenyl)-7-methoxy-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
123549-17-7

2D Structure

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2D Structure of Artonin U

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8808 88.08%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8025 80.25%
OATP2B1 inhibitior - 0.7052 70.52%
OATP1B1 inhibitior + 0.8678 86.78%
OATP1B3 inhibitior + 0.8489 84.89%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7720 77.20%
P-glycoprotein inhibitior + 0.7403 74.03%
P-glycoprotein substrate - 0.7215 72.15%
CYP3A4 substrate + 0.5748 57.48%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7744 77.44%
CYP2C9 inhibition + 0.9095 90.95%
CYP2C19 inhibition + 0.9477 94.77%
CYP2D6 inhibition - 0.6328 63.28%
CYP1A2 inhibition + 0.8370 83.70%
CYP2C8 inhibition + 0.7378 73.78%
CYP inhibitory promiscuity + 0.9465 94.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6303 63.03%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.5574 55.74%
Skin irritation - 0.7822 78.22%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4121 41.21%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8334 83.34%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6368 63.68%
Acute Oral Toxicity (c) III 0.7450 74.50%
Estrogen receptor binding + 0.9065 90.65%
Androgen receptor binding + 0.8945 89.45%
Thyroid receptor binding + 0.5858 58.58%
Glucocorticoid receptor binding + 0.8566 85.66%
Aromatase binding + 0.7962 79.62%
PPAR gamma + 0.9272 92.72%
Honey bee toxicity - 0.6935 69.35%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9919 99.19%

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 98.44% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.01% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.55% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.38% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.70% 86.33%
CHEMBL3194 P02766 Transthyretin 92.70% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.75% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.69% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.47% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.59% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.40% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.11% 99.15%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.01% 97.28%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.53% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.70% 93.99%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.76% 86.92%

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 chama
Artocarpus heterophyllus

Cross-Links

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PubChem 44258358
LOTUS LTS0217656
wikiData Q104945485