Allopatuletin

Details

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Internal ID 2afaa226-2ded-411b-9956-c776184d76e7
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 2-(3,4-dihydroxyphenyl)-3,6,7-trihydroxy-5-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O8/c1-23-16-11-10(5-9(19)12(16)20)24-15(14(22)13(11)21)6-2-3-7(17)8(18)4-6/h2-5,17-20,22H,1H3
InChI Key AFVIGTXOPSJUAS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O8
Molecular Weight 332.26 g/mol
Exact Mass 332.05321734 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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CHEBI:196349
LMPK12112985
3,6,7,3',4'-pentahydroxy-5-methoxyflavone
2-(3,4-dihydroxyphenyl)-3,6,7-trihydroxy-5-methoxychromen-4-one

2D Structure

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2D Structure of Allopatuletin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9577 95.77%
Caco-2 - 0.7346 73.46%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7944 79.44%
OATP2B1 inhibitior + 0.5869 58.69%
OATP1B1 inhibitior + 0.9576 95.76%
OATP1B3 inhibitior + 0.9965 99.65%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8137 81.37%
P-glycoprotein inhibitior - 0.8187 81.87%
P-glycoprotein substrate - 0.8625 86.25%
CYP3A4 substrate + 0.5402 54.02%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.7179 71.79%
CYP2C9 inhibition + 0.5494 54.94%
CYP2C19 inhibition + 0.6827 68.27%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition + 0.9263 92.63%
CYP2C8 inhibition + 0.8936 89.36%
CYP inhibitory promiscuity + 0.6056 60.56%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5596 55.96%
Eye corrosion - 0.9766 97.66%
Eye irritation + 0.7109 71.09%
Skin irritation - 0.5899 58.99%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7172 71.72%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9318 93.18%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8916 89.16%
Acute Oral Toxicity (c) III 0.6733 67.33%
Estrogen receptor binding + 0.8939 89.39%
Androgen receptor binding + 0.8394 83.94%
Thyroid receptor binding + 0.5695 56.95%
Glucocorticoid receptor binding + 0.8683 86.83%
Aromatase binding + 0.6313 63.13%
PPAR gamma + 0.8111 81.11%
Honey bee toxicity - 0.8878 88.78%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8838 88.38%

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 99.67% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.47% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.99% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.41% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.95% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.57% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.82% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.65% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 87.08% 91.49%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.99% 80.78%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.68% 98.11%
CHEMBL3194 P02766 Transthyretin 85.60% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 83.22% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.23% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.75% 99.17%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.17% 95.64%

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.
Tagetes erecta

Cross-Links

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PubChem 44259868
LOTUS LTS0034027
wikiData Q104911583