Pratensin A

Details

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Internal ID 2500187a-8dca-4845-a5f9-ba0fcf55720e
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name [5,7-dihydroxy-3,6-dimethoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H22O9/c1-6-11(2)23(27)32-22-17(26)20(29-4)15(24)14-16(25)21(30-5)18(31-19(14)22)12-7-9-13(28-3)10-8-12/h6-10,24,26H,1-5H3/b11-6+
InChI Key MJKSKSYTKXRLCZ-IZZDOVSWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O9
Molecular Weight 442.40 g/mol
Exact Mass 442.12638228 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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5,7,8-Trihydroxy-3,6,4'-trimethoxyflavone 8-tiglate
CHEBI:166636
LMPK12113306
[5,7-dihydroxy-3,6-dimethoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl] (E)-2-methylbut-2-enoate

2D Structure

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2D Structure of Pratensin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9439 94.39%
Caco-2 + 0.5748 57.48%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5649 56.49%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.8769 87.69%
OATP1B3 inhibitior + 0.8643 86.43%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6834 68.34%
P-glycoprotein inhibitior + 0.8813 88.13%
P-glycoprotein substrate - 0.7806 78.06%
CYP3A4 substrate + 0.5992 59.92%
CYP2C9 substrate - 0.5903 59.03%
CYP2D6 substrate - 0.8757 87.57%
CYP3A4 inhibition - 0.7105 71.05%
CYP2C9 inhibition - 0.6213 62.13%
CYP2C19 inhibition + 0.5469 54.69%
CYP2D6 inhibition - 0.8841 88.41%
CYP1A2 inhibition - 0.6721 67.21%
CYP2C8 inhibition + 0.6376 63.76%
CYP inhibitory promiscuity + 0.7649 76.49%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.5413 54.13%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.7303 73.03%
Skin irritation - 0.7168 71.68%
Skin corrosion - 0.9582 95.82%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4730 47.30%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8782 87.82%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5195 51.95%
Acute Oral Toxicity (c) III 0.4228 42.28%
Estrogen receptor binding + 0.8933 89.33%
Androgen receptor binding + 0.7751 77.51%
Thyroid receptor binding + 0.6983 69.83%
Glucocorticoid receptor binding + 0.8633 86.33%
Aromatase binding + 0.6806 68.06%
PPAR gamma + 0.7479 74.79%
Honey bee toxicity - 0.8195 81.95%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9851 98.51%

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 99.16% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.25% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.67% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.65% 89.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.40% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.02% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.51% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.37% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.63% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.30% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.89% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.98% 99.15%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.32% 85.30%
CHEMBL3401 O75469 Pregnane X receptor 82.45% 94.73%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.65% 94.42%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.95% 80.96%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.91% 98.11%

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.
Galeana pratensis

Cross-Links

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PubChem 15736235
LOTUS LTS0049402
wikiData Q76506895