Flavone base + 3O, 1MeO, O-MalonylHex

Details

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Internal ID 41841c31-6739-432d-a4e6-dd7153bcc5f4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 3-oxo-3-[[3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H24O14/c1-35-16-4-10(2-3-12(16)26)15-7-14(28)21-13(27)5-11(6-17(21)38-15)37-25-24(34)23(33)22(32)18(39-25)9-36-20(31)8-19(29)30/h2-7,18,22-27,32-34H,8-9H2,1H3,(H,29,30)
InChI Key PLQBKZOSLQNLOX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O14
Molecular Weight 548.40 g/mol
Exact Mass 548.11660544 g/mol
Topological Polar Surface Area (TPSA) 219.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.08
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Flavone base + 3O, 1MeO, O-MalonylHex

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4650 46.50%
Caco-2 - 0.9015 90.15%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6150 61.50%
OATP2B1 inhibitior - 0.5639 56.39%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6474 64.74%
P-glycoprotein inhibitior + 0.5826 58.26%
P-glycoprotein substrate - 0.5129 51.29%
CYP3A4 substrate + 0.6075 60.75%
CYP2C9 substrate - 0.6278 62.78%
CYP2D6 substrate - 0.8638 86.38%
CYP3A4 inhibition - 0.8782 87.82%
CYP2C9 inhibition - 0.9310 93.10%
CYP2C19 inhibition - 0.9222 92.22%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.9104 91.04%
CYP2C8 inhibition + 0.8002 80.02%
CYP inhibitory promiscuity - 0.9238 92.38%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6500 65.00%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9093 90.93%
Skin irritation - 0.8282 82.82%
Skin corrosion - 0.9516 95.16%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4147 41.47%
Micronuclear + 0.6918 69.18%
Hepatotoxicity - 0.8448 84.48%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.9179 91.79%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.8236 82.36%
Androgen receptor binding + 0.5886 58.86%
Thyroid receptor binding - 0.5515 55.15%
Glucocorticoid receptor binding + 0.6923 69.23%
Aromatase binding + 0.6077 60.77%
PPAR gamma + 0.6934 69.34%
Honey bee toxicity - 0.7771 77.71%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6949 69.49%
Fish aquatic toxicity + 0.9093 90.93%

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 99.19% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.02% 85.14%
CHEMBL220 P22303 Acetylcholinesterase 97.34% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.96% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.65% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.72% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.72% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.73% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.71% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.77% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.88% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.56% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.99% 96.00%
CHEMBL3194 P02766 Transthyretin 85.00% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 84.32% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.14% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.01% 95.89%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.33% 94.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.98% 86.92%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.47% 97.36%
CHEMBL5255 O00206 Toll-like receptor 4 81.22% 92.50%
CHEMBL340 P08684 Cytochrome P450 3A4 81.21% 91.19%

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.
Stratiotes aloides

Cross-Links

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PubChem 74977711
LOTUS LTS0259350
wikiData Q105211133