Luteolin 7-lactate

Details

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Internal ID 42ee0fe1-e15b-431f-8222-d38e644a3022
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones
IUPAC Name [2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl] 2-hydroxypropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O8/c1-8(19)18(24)25-10-5-13(22)17-14(23)7-15(26-16(17)6-10)9-2-3-11(20)12(21)4-9/h2-8,19-22H,1H3
InChI Key RWLCWWWLTRAVKI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O8
Molecular Weight 358.30 g/mol
Exact Mass 358.06886740 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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LMPK12110733

2D Structure

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2D Structure of Luteolin 7-lactate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8979 89.79%
Caco-2 - 0.6502 65.02%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8132 81.32%
OATP2B1 inhibitior + 0.5768 57.68%
OATP1B1 inhibitior + 0.9542 95.42%
OATP1B3 inhibitior + 0.9849 98.49%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5498 54.98%
P-glycoprotein inhibitior - 0.7057 70.57%
P-glycoprotein substrate - 0.8387 83.87%
CYP3A4 substrate + 0.5329 53.29%
CYP2C9 substrate + 0.5895 58.95%
CYP2D6 substrate - 0.8784 87.84%
CYP3A4 inhibition - 0.9491 94.91%
CYP2C9 inhibition + 0.5378 53.78%
CYP2C19 inhibition - 0.7939 79.39%
CYP2D6 inhibition - 0.9740 97.40%
CYP1A2 inhibition + 0.5875 58.75%
CYP2C8 inhibition + 0.6072 60.72%
CYP inhibitory promiscuity - 0.8109 81.09%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6076 60.76%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.6660 66.60%
Skin irritation - 0.6536 65.36%
Skin corrosion - 0.9349 93.49%
Ames mutagenesis - 0.5664 56.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6630 66.30%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9403 94.03%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6949 69.49%
Acute Oral Toxicity (c) III 0.5586 55.86%
Estrogen receptor binding + 0.8095 80.95%
Androgen receptor binding + 0.9043 90.43%
Thyroid receptor binding + 0.5629 56.29%
Glucocorticoid receptor binding + 0.7867 78.67%
Aromatase binding + 0.7310 73.10%
PPAR gamma + 0.7051 70.51%
Honey bee toxicity - 0.6563 65.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7050 70.50%
Fish aquatic toxicity + 0.9764 97.64%

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 98.48% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.64% 99.15%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.40% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.09% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.04% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.14% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.40% 90.71%
CHEMBL3194 P02766 Transthyretin 90.68% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.54% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.39% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 88.68% 94.73%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.29% 85.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.99% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.21% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.47% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.18% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.95% 86.92%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.85% 95.71%

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.
Marrubium vulgare

Cross-Links

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PubChem 44258150
LOTUS LTS0046267
wikiData Q105246556