Luteolin 7-O-(6''-malonylglucoside)

Details

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Internal ID bc0a4cee-56a4-4fb1-b97d-eddcd4973aee
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 3-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid
SMILES (Canonical) C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)COC(=O)CC(=O)O)O)O)O)O)O)O
InChI InChI=1S/C24H22O14/c25-11-2-1-9(3-12(11)26)15-6-14(28)20-13(27)4-10(5-16(20)37-15)36-24-23(34)22(33)21(32)17(38-24)8-35-19(31)7-18(29)30/h1-6,17,21-27,32-34H,7-8H2,(H,29,30)/t17-,21-,22+,23-,24-/m1/s1
InChI Key RNDGJCZQVKFBPI-ASDZUOGYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H22O14
Molecular Weight 534.40 g/mol
Exact Mass 534.10095537 g/mol
Topological Polar Surface Area (TPSA) 230.00 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.22
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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98767-38-5
luteolin 7-O-(6-O-malonyl-beta-D-glucoside)
luteolin 7-O-(6-malonyl-beta-D-glucoside)
3-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid
luteolin 7-O-beta-D-(6''-O-malonyl) glucopyranoside
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl 6-O-(carboxyacetyl)-beta-D-glucopyranoside
Luteolin 7-malonylglucoside
CHEBI:6579
DTXSID80415173
Q27107251

2D Structure

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2D Structure of Luteolin 7-O-(6''-malonylglucoside)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5156 51.56%
Caco-2 - 0.9099 90.99%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5919 59.19%
OATP2B1 inhibitior - 0.5517 55.17%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9243 92.43%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6328 63.28%
P-glycoprotein inhibitior - 0.4598 45.98%
P-glycoprotein substrate - 0.6791 67.91%
CYP3A4 substrate + 0.5934 59.34%
CYP2C9 substrate + 0.5635 56.35%
CYP2D6 substrate - 0.8684 86.84%
CYP3A4 inhibition - 0.8731 87.31%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9222 92.22%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.9262 92.62%
CYP2C8 inhibition + 0.7822 78.22%
CYP inhibitory promiscuity - 0.9340 93.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6855 68.55%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.8817 88.17%
Skin irritation - 0.8213 82.13%
Skin corrosion - 0.9590 95.90%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4617 46.17%
Micronuclear + 0.7118 71.18%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9103 91.03%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.9220 92.20%
Acute Oral Toxicity (c) III 0.4846 48.46%
Estrogen receptor binding + 0.8039 80.39%
Androgen receptor binding + 0.6599 65.99%
Thyroid receptor binding - 0.5216 52.16%
Glucocorticoid receptor binding + 0.6510 65.10%
Aromatase binding + 0.5898 58.98%
PPAR gamma + 0.7269 72.69%
Honey bee toxicity - 0.7472 74.72%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6950 69.50%
Fish aquatic toxicity + 0.9497 94.97%

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 99.65% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.38% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 96.09% 91.49%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.24% 89.00%
CHEMBL220 P22303 Acetylcholinesterase 92.52% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.31% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.21% 99.17%
CHEMBL3194 P02766 Transthyretin 88.20% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 87.01% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.61% 90.71%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 86.34% 95.64%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.56% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.87% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.52% 97.09%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 82.72% 80.33%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.35% 83.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.32% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.01% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 80.72% 92.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.33% 99.23%

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.
Elsholtzia ciliata
Stratiotes aloides

Cross-Links

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PubChem 5281669
NPASS NPC229409
LOTUS LTS0266290
wikiData Q27107251