5,4'-Dihydroxy-3,7,3'-trimethoxy-8-prenylflavone

Details

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Internal ID 2114389c-2b15-4448-8f65-2ca1155ee4dd
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O7/c1-12(2)6-8-14-17(27-3)11-16(25)19-20(26)23(29-5)21(30-22(14)19)13-7-9-15(24)18(10-13)28-4/h6-7,9-11,24-25H,8H2,1-5H3
InChI Key PXSHTLGJABJXLY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H24O7
Molecular Weight 412.40 g/mol
Exact Mass 412.15220310 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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LMPK12112745

2D Structure

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2D Structure of 5,4'-Dihydroxy-3,7,3'-trimethoxy-8-prenylflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.7654 76.54%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7007 70.07%
OATP2B1 inhibitior - 0.7157 71.57%
OATP1B1 inhibitior + 0.9302 93.02%
OATP1B3 inhibitior + 0.8634 86.34%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8646 86.46%
P-glycoprotein inhibitior + 0.8463 84.63%
P-glycoprotein substrate - 0.7673 76.73%
CYP3A4 substrate + 0.5557 55.57%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8014 80.14%
CYP2C9 inhibition + 0.8898 88.98%
CYP2C19 inhibition + 0.9435 94.35%
CYP2D6 inhibition - 0.5726 57.26%
CYP1A2 inhibition + 0.7497 74.97%
CYP2C8 inhibition + 0.7309 73.09%
CYP inhibitory promiscuity + 0.9246 92.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6363 63.63%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.5324 53.24%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9621 96.21%
Ames mutagenesis - 0.5137 51.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6128 61.28%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8209 82.09%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6782 67.82%
Acute Oral Toxicity (c) III 0.7315 73.15%
Estrogen receptor binding + 0.9293 92.93%
Androgen receptor binding + 0.7823 78.23%
Thyroid receptor binding + 0.6113 61.13%
Glucocorticoid receptor binding + 0.8842 88.42%
Aromatase binding + 0.6997 69.97%
PPAR gamma + 0.8658 86.58%
Honey bee toxicity - 0.8075 80.75%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9888 98.88%

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 99.28% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.84% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.32% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.04% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.13% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.27% 89.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.26% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.01% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 90.67% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.84% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.16% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.72% 96.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.77% 96.12%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.90% 85.30%
CHEMBL3194 P02766 Transthyretin 84.01% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.24% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.57% 95.50%

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.
Leionema dentatum

Cross-Links

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PubChem 44259690
LOTUS LTS0040657
wikiData Q105216346