[3,4-Bis[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Details

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Internal ID 8a417f24-9f17-4508-ba28-84630a8d6fed
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name [3,4-bis[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H46O20/c1-54-28-16-22(4-10-25(28)45)7-13-33(48)57-20-32-39(59-34(49)14-8-23-5-11-26(46)29(17-23)55-2)40(60-35(50)15-9-24-6-12-27(47)30(18-24)56-3)42(21-44,61-32)62-41-38(53)37(52)36(51)31(19-43)58-41/h4-18,31-32,36-41,43-47,51-53H,19-21H2,1-3H3
InChI Key QKDVORUGRIVQPJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H46O20
Molecular Weight 870.80 g/mol
Exact Mass 870.25824385 g/mol
Topological Polar Surface Area (TPSA) 296.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 0.54
H-Bond Acceptor 20
H-Bond Donor 8
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [3,4-Bis[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7827 78.27%
Caco-2 - 0.8811 88.11%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.7023 70.23%
OATP2B1 inhibitior + 0.5587 55.87%
OATP1B1 inhibitior + 0.8557 85.57%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9162 91.62%
P-glycoprotein inhibitior + 0.7558 75.58%
P-glycoprotein substrate - 0.7030 70.30%
CYP3A4 substrate + 0.6582 65.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8593 85.93%
CYP3A4 inhibition - 0.7802 78.02%
CYP2C9 inhibition - 0.8269 82.69%
CYP2C19 inhibition - 0.8158 81.58%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition - 0.8796 87.96%
CYP2C8 inhibition + 0.7438 74.38%
CYP inhibitory promiscuity - 0.7421 74.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6433 64.33%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9101 91.01%
Skin irritation - 0.8527 85.27%
Skin corrosion - 0.9546 95.46%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7874 78.74%
Micronuclear - 0.5426 54.26%
Hepatotoxicity - 0.8824 88.24%
skin sensitisation - 0.8251 82.51%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.9195 91.95%
Acute Oral Toxicity (c) III 0.6316 63.16%
Estrogen receptor binding + 0.8040 80.40%
Androgen receptor binding + 0.6409 64.09%
Thyroid receptor binding + 0.5982 59.82%
Glucocorticoid receptor binding + 0.6799 67.99%
Aromatase binding + 0.5321 53.21%
PPAR gamma + 0.7432 74.32%
Honey bee toxicity - 0.7108 71.08%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9374 93.74%

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 99.66% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.61% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.60% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.20% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.98% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.30% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.58% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 90.86% 94.73%
CHEMBL4208 P20618 Proteasome component C5 89.56% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.13% 99.17%
CHEMBL3194 P02766 Transthyretin 88.71% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.72% 97.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.17% 97.36%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.84% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.91% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.29% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.98% 92.62%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.37% 89.62%

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.
Smilax riparia

Cross-Links

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PubChem 78072352
LOTUS LTS0025070
wikiData Q105223035