[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Details

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Internal ID 605a8685-a8d1-4cdb-a4e3-b7e09c8dad24
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Hydroxycinnamic acid glycosides
IUPAC Name [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)/C=C/C(=O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O
InChI InChI=1S/C24H26O14/c1-34-14-5-10(6-15(35-2)19(14)29)3-4-17(27)38-24-22(32)21(31)20(30)16(37-24)9-36-23(33)11-7-12(25)18(28)13(26)8-11/h3-8,16,20-22,24-26,28-32H,9H2,1-2H3/b4-3+/t16-,20-,21+,22-,24+/m1/s1
InChI Key SCXUKRFESVSQSS-UGVHACPXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O14
Molecular Weight 538.50 g/mol
Exact Mass 538.13225550 g/mol
Topological Polar Surface Area (TPSA) 222.00 Ų
XlogP 0.30
Atomic LogP (AlogP) -0.25
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6714 67.14%
Caco-2 - 0.8712 87.12%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6293 62.93%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.7122 71.22%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7506 75.06%
P-glycoprotein inhibitior - 0.4397 43.97%
P-glycoprotein substrate - 0.7504 75.04%
CYP3A4 substrate + 0.5882 58.82%
CYP2C9 substrate - 0.6023 60.23%
CYP2D6 substrate - 0.8483 84.83%
CYP3A4 inhibition - 0.7161 71.61%
CYP2C9 inhibition - 0.7544 75.44%
CYP2C19 inhibition - 0.8048 80.48%
CYP2D6 inhibition - 0.8692 86.92%
CYP1A2 inhibition - 0.8150 81.50%
CYP2C8 inhibition + 0.7480 74.80%
CYP inhibitory promiscuity - 0.7330 73.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7527 75.27%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.8858 88.58%
Skin irritation - 0.8541 85.41%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3951 39.51%
Micronuclear + 0.6666 66.66%
Hepatotoxicity - 0.7716 77.16%
skin sensitisation - 0.8758 87.58%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.9693 96.93%
Acute Oral Toxicity (c) III 0.7357 73.57%
Estrogen receptor binding + 0.6719 67.19%
Androgen receptor binding + 0.5271 52.71%
Thyroid receptor binding + 0.5242 52.42%
Glucocorticoid receptor binding + 0.6834 68.34%
Aromatase binding - 0.5170 51.70%
PPAR gamma + 0.5487 54.87%
Honey bee toxicity - 0.8497 84.97%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9442 94.42%

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 99.22% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.12% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.09% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.71% 86.33%
CHEMBL3194 P02766 Transthyretin 94.14% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 93.12% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.91% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.57% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.86% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 87.33% 92.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.23% 97.36%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.99% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.51% 95.89%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 82.25% 98.21%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.01% 97.21%
CHEMBL4208 P20618 Proteasome component C5 81.93% 90.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.95% 85.31%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.84% 94.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.52% 92.94%

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.
Myriophyllum verticillatum

Cross-Links

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PubChem 15126899
LOTUS LTS0041717
wikiData Q105250488