[6-[(4-Ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

Details

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Internal ID 83e27c3e-7940-4fe1-8619-809334258d20
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name [6-[(4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES (Canonical) C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O
SMILES (Isomeric) C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O
InChI InChI=1S/C25H28O13/c1-2-13-23(35-11-14-22(32)34-8-7-25(13,14)33)38-24-20(31)19(30)21(17(10-26)36-24)37-18(29)6-4-12-3-5-15(27)16(28)9-12/h2-6,9,11,13,17,19-21,23-24,26-28,30-31,33H,1,7-8,10H2
InChI Key XXXYWVBHDRFERD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H28O13
Molecular Weight 536.50 g/mol
Exact Mass 536.15299094 g/mol
Topological Polar Surface Area (TPSA) 202.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.80
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [6-[(4-Ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-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 + 0.7640 76.40%
Caco-2 - 0.9036 90.36%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7418 74.18%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.8709 87.09%
OATP1B3 inhibitior + 0.9298 92.98%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8096 80.96%
BSEP inhibitior - 0.7157 71.57%
P-glycoprotein inhibitior - 0.4915 49.15%
P-glycoprotein substrate - 0.5981 59.81%
CYP3A4 substrate + 0.6895 68.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8694 86.94%
CYP3A4 inhibition - 0.8084 80.84%
CYP2C9 inhibition - 0.6653 66.53%
CYP2C19 inhibition - 0.6200 62.00%
CYP2D6 inhibition - 0.8081 80.81%
CYP1A2 inhibition - 0.7108 71.08%
CYP2C8 inhibition + 0.6736 67.36%
CYP inhibitory promiscuity - 0.9067 90.67%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6006 60.06%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.8953 89.53%
Skin irritation - 0.7556 75.56%
Skin corrosion - 0.9342 93.42%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5669 56.69%
Micronuclear - 0.5867 58.67%
Hepatotoxicity - 0.6226 62.26%
skin sensitisation - 0.7605 76.05%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8946 89.46%
Acute Oral Toxicity (c) III 0.5001 50.01%
Estrogen receptor binding + 0.7883 78.83%
Androgen receptor binding + 0.7135 71.35%
Thyroid receptor binding - 0.4937 49.37%
Glucocorticoid receptor binding + 0.6633 66.33%
Aromatase binding + 0.6049 60.49%
PPAR gamma + 0.7096 70.96%
Honey bee toxicity - 0.6471 64.71%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8966 89.66%

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 99.82% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.08% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.90% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.92% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.42% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.57% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.53% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.99% 96.09%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 87.13% 97.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.11% 92.62%
CHEMBL2581 P07339 Cathepsin D 85.24% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.30% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.76% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.71% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.71% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.07% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.74% 91.07%
CHEMBL4530 P00488 Coagulation factor XIII 80.71% 96.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162978412
LOTUS LTS0147180
wikiData Q105344275