3',4',5,7-Tetrahydroxy-3-(2-O-galloyl-alpha-L-arabinopyranosyloxy)flavone

Details

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Internal ID 33fdef9c-b464-4647-9589-718d9cb400b6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name [(2S,3R,4S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O
SMILES (Isomeric) C1[C@@H]([C@@H]([C@H]([C@@H](O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O
InChI InChI=1S/C27H22O15/c28-11-6-14(31)19-18(7-11)40-23(9-1-2-12(29)13(30)3-9)24(22(19)37)42-27-25(21(36)17(34)8-39-27)41-26(38)10-4-15(32)20(35)16(33)5-10/h1-7,17,21,25,27-36H,8H2/t17-,21-,25+,27-/m0/s1
InChI Key XLHGECRFSYAHQI-LEYCRWIUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H22O15
Molecular Weight 586.50 g/mol
Exact Mass 586.09586999 g/mol
Topological Polar Surface Area (TPSA) 253.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.08
H-Bond Acceptor 15
H-Bond Donor 9
Rotatable Bonds 5

Synonyms

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BDBM50478872
3',4',5,7-Tetrahydroxy-3-(2-O-galloyl-alpha-L-arabinopyranosyloxy)flavone

2D Structure

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2D Structure of 3',4',5,7-Tetrahydroxy-3-(2-O-galloyl-alpha-L-arabinopyranosyloxy)flavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7471 74.71%
Caco-2 - 0.9000 90.00%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5672 56.72%
OATP2B1 inhibitior + 0.5854 58.54%
OATP1B1 inhibitior + 0.8003 80.03%
OATP1B3 inhibitior + 0.8791 87.91%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8012 80.12%
P-glycoprotein inhibitior + 0.7216 72.16%
P-glycoprotein substrate + 0.5367 53.67%
CYP3A4 substrate + 0.6892 68.92%
CYP2C9 substrate - 0.6458 64.58%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition - 0.9270 92.70%
CYP2C9 inhibition - 0.9485 94.85%
CYP2C19 inhibition - 0.9368 93.68%
CYP2D6 inhibition - 0.9576 95.76%
CYP1A2 inhibition - 0.9384 93.84%
CYP2C8 inhibition + 0.9285 92.85%
CYP inhibitory promiscuity - 0.9623 96.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7024 70.24%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8592 85.92%
Skin irritation - 0.7891 78.91%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8134 81.34%
Micronuclear + 0.8033 80.33%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.9802 98.02%
Acute Oral Toxicity (c) III 0.4729 47.29%
Estrogen receptor binding + 0.7878 78.78%
Androgen receptor binding + 0.8151 81.51%
Thyroid receptor binding - 0.4921 49.21%
Glucocorticoid receptor binding + 0.6197 61.97%
Aromatase binding - 0.5717 57.17%
PPAR gamma + 0.6879 68.79%
Honey bee toxicity - 0.7586 75.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5050 50.50%
Fish aquatic toxicity + 0.8862 88.62%

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 99.73% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.61% 91.49%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 99.13% 95.64%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.65% 89.00%
CHEMBL3194 P02766 Transthyretin 95.79% 90.71%
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 93.02% 83.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.43% 94.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 92.40% 95.78%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.96% 99.15%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.76% 94.42%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 89.52% 97.53%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.42% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.72% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.65% 90.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.48% 95.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.92% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.70% 97.09%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.26% 80.78%
CHEMBL4208 P20618 Proteasome component C5 86.06% 90.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 83.41% 96.12%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.47% 95.53%
CHEMBL340 P08684 Cytochrome P450 3A4 81.30% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.27% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.46% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.35% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.15% 100.00%

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.
Cynoglossum germanicum
Eucalyptus camaldulensis subsp. camaldulensis
Euphorbia watanabei
Larix decidua
Leontopodium nanum
Strophanthus preussii

Cross-Links

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PubChem 9985767
NPASS NPC144097
LOTUS LTS0098293
wikiData Q105329979