[4-[[(3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl]-2-methoxyphenyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Details

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Internal ID a78afdf7-a94e-4ede-ab13-baab6a763d62
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans
IUPAC Name [4-[[(3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl]-2-methoxyphenyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
SMILES (Canonical) COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)OC(=O)C=CC4=CC(=C(C=C4)O)OC)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C[C@H]2COC[C@@H]2CC3=CC(=C(C=C3)OC(=O)/C=C/C4=CC(=C(C=C4)O)OC)OC)O
InChI InChI=1S/C30H32O8/c1-34-27-14-19(4-8-24(27)31)7-11-30(33)38-26-10-6-21(16-29(26)36-3)13-23-18-37-17-22(23)12-20-5-9-25(32)28(15-20)35-2/h4-11,14-16,22-23,31-32H,12-13,17-18H2,1-3H3/b11-7+/t22-,23-/m0/s1
InChI Key WUMFMXNTYLFVSJ-ZDRWSHPDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H32O8
Molecular Weight 520.60 g/mol
Exact Mass 520.20971797 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [4-[[(3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl]-2-methoxyphenyl] (E)-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 + 0.9665 96.65%
Caco-2 - 0.7780 77.80%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8769 87.69%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9151 91.51%
OATP1B3 inhibitior + 0.9043 90.43%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9162 91.62%
P-glycoprotein inhibitior + 0.9058 90.58%
P-glycoprotein substrate - 0.7097 70.97%
CYP3A4 substrate + 0.5758 57.58%
CYP2C9 substrate + 0.6039 60.39%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition + 0.7522 75.22%
CYP2C9 inhibition + 0.7216 72.16%
CYP2C19 inhibition + 0.7807 78.07%
CYP2D6 inhibition - 0.8481 84.81%
CYP1A2 inhibition + 0.5718 57.18%
CYP2C8 inhibition + 0.8305 83.05%
CYP inhibitory promiscuity + 0.8499 84.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8645 86.45%
Carcinogenicity (trinary) Non-required 0.5645 56.45%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9186 91.86%
Skin irritation - 0.8707 87.07%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8674 86.74%
Micronuclear + 0.5374 53.74%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.7773 77.73%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5752 57.52%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.8776 87.76%
Acute Oral Toxicity (c) III 0.5970 59.70%
Estrogen receptor binding + 0.8462 84.62%
Androgen receptor binding + 0.7712 77.12%
Thyroid receptor binding + 0.6075 60.75%
Glucocorticoid receptor binding + 0.7386 73.86%
Aromatase binding - 0.5869 58.69%
PPAR gamma + 0.6128 61.28%
Honey bee toxicity - 0.7633 76.33%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5145 51.45%
Fish aquatic toxicity + 0.9939 99.39%

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 98.89% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.71% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.02% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.79% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.75% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.54% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.64% 98.95%
CHEMBL3194 P02766 Transthyretin 90.44% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.84% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.60% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.69% 92.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.53% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.31% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.27% 92.94%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.31% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.09% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.80% 96.95%
CHEMBL2179 P04062 Beta-glucocerebrosidase 81.47% 85.31%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.42% 80.78%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.30% 89.50%

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.
Diospyros kaki

Cross-Links

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PubChem 163187147
LOTUS LTS0067194
wikiData Q105313146