methyl 3-ethenyl-4-[2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate

Details

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Internal ID 5d75a0ea-3705-49e2-9b17-1eb0bdab7324
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name methyl 3-ethenyl-4-[2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate
SMILES (Canonical) COC1=C(C=CC(=C1)C=CC(=O)OCCC2C(C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)C=C)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C=CC(=O)OCCC2C(C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)C=C)O
InChI InChI=1S/C27H34O13/c1-4-15-16(9-10-37-21(30)8-6-14-5-7-18(29)19(11-14)35-2)17(25(34)36-3)13-38-26(15)40-27-24(33)23(32)22(31)20(12-28)39-27/h4-8,11,13,15-16,20,22-24,26-29,31-33H,1,9-10,12H2,2-3H3
InChI Key KEKNHVHEPJLKLM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O13
Molecular Weight 566.50 g/mol
Exact Mass 566.19994113 g/mol
Topological Polar Surface Area (TPSA) 191.00 Ų
XlogP 0.90
Atomic LogP (AlogP) -0.00
H-Bond Acceptor 13
H-Bond Donor 5
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 3-ethenyl-4-[2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7378 73.78%
Caco-2 - 0.8800 88.00%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7030 70.30%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8155 81.55%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6508 65.08%
P-glycoprotein inhibitior - 0.4556 45.56%
P-glycoprotein substrate - 0.5146 51.46%
CYP3A4 substrate + 0.6812 68.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8593 85.93%
CYP3A4 inhibition - 0.8196 81.96%
CYP2C9 inhibition - 0.6974 69.74%
CYP2C19 inhibition - 0.7215 72.15%
CYP2D6 inhibition - 0.8927 89.27%
CYP1A2 inhibition - 0.8157 81.57%
CYP2C8 inhibition + 0.8188 81.88%
CYP inhibitory promiscuity - 0.8176 81.76%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7462 74.62%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9343 93.43%
Skin irritation - 0.8138 81.38%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis - 0.5778 57.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4036 40.36%
Micronuclear - 0.6767 67.67%
Hepatotoxicity - 0.7789 77.89%
skin sensitisation - 0.7915 79.15%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6501 65.01%
Acute Oral Toxicity (c) III 0.6739 67.39%
Estrogen receptor binding + 0.8521 85.21%
Androgen receptor binding + 0.7171 71.71%
Thyroid receptor binding + 0.6092 60.92%
Glucocorticoid receptor binding + 0.7319 73.19%
Aromatase binding - 0.5219 52.19%
PPAR gamma + 0.7095 70.95%
Honey bee toxicity - 0.7581 75.81%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8433 84.33%

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 99.24% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.64% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.21% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 96.82% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.54% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.92% 89.00%
CHEMBL3194 P02766 Transthyretin 89.71% 90.71%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.75% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 86.63% 94.73%
CHEMBL4208 P20618 Proteasome component C5 84.68% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.71% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.40% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.86% 94.45%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 81.82% 95.83%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.82% 95.89%
CHEMBL220 P22303 Acetylcholinesterase 80.42% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.29% 95.56%
CHEMBL5028 O14672 ADAM10 80.05% 97.50%

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.
Exacum tetragonum

Cross-Links

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PubChem 163039456
LOTUS LTS0189210
wikiData Q105140011