[2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

Details

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Internal ID 04692348-52c4-40f5-a26f-488774964a73
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name [2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES (Canonical) C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O
SMILES (Isomeric) C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O
InChI InChI=1S/C25H28O12/c1-2-13-14-7-8-33-23(32)15(14)11-34-24(13)37-25-21(31)22(20(30)18(10-26)35-25)36-19(29)6-4-12-3-5-16(27)17(28)9-12/h2-6,9,11,13-14,18,20-22,24-28,30-31H,1,7-8,10H2
InChI Key XOGGREZGCFWEBP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H28O12
Molecular Weight 520.50 g/mol
Exact Mass 520.15807632 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.08
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] 3-(3,4-dihydroxyphenyl)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 + 0.6825 68.25%
Caco-2 - 0.8957 89.57%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6689 66.89%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.8602 86.02%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5602 56.02%
P-glycoprotein inhibitior - 0.5153 51.53%
P-glycoprotein substrate - 0.6440 64.40%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition - 0.8345 83.45%
CYP2C9 inhibition - 0.6973 69.73%
CYP2C19 inhibition - 0.6672 66.72%
CYP2D6 inhibition - 0.8587 85.87%
CYP1A2 inhibition - 0.7516 75.16%
CYP2C8 inhibition + 0.7175 71.75%
CYP inhibitory promiscuity - 0.8098 80.98%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6957 69.57%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.9103 91.03%
Skin irritation - 0.7829 78.29%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5645 56.45%
Micronuclear - 0.5967 59.67%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.7304 73.04%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7892 78.92%
Acute Oral Toxicity (c) III 0.5006 50.06%
Estrogen receptor binding + 0.7806 78.06%
Androgen receptor binding + 0.7124 71.24%
Thyroid receptor binding + 0.5605 56.05%
Glucocorticoid receptor binding + 0.6449 64.49%
Aromatase binding + 0.5204 52.04%
PPAR gamma + 0.7369 73.69%
Honey bee toxicity - 0.7405 74.05%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9089 90.89%

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 99.71% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.01% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.88% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.60% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.99% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.55% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.45% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.12% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.48% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.94% 86.92%
CHEMBL226 P30542 Adenosine A1 receptor 87.89% 95.93%
CHEMBL2581 P07339 Cathepsin D 87.68% 98.95%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 85.37% 97.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.28% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.85% 100.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.84% 95.83%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.48% 99.17%
CHEMBL3194 P02766 Transthyretin 80.34% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.18% 96.21%

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.
Neolamarckia cadamba

Cross-Links

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PubChem 85183017
LOTUS LTS0193237
wikiData Q105337734