2-[4-[2-(4-Hydroxy-3,5-dimethoxyphenyl)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-5-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 9bd5bef7-d022-4dce-a47c-3cd0004b655b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-[4-[2-(4-hydroxy-3,5-dimethoxyphenyl)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-5-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C2CC3C(O2)CC(O3)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C2CC3C(O2)CC(O3)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC
InChI InChI=1S/C28H36O13/c1-34-18-5-12(6-19(35-2)23(18)30)14-9-16-17(38-14)10-15(39-16)13-7-20(36-3)27(21(8-13)37-4)41-28-26(33)25(32)24(31)22(11-29)40-28/h5-8,14-17,22,24-26,28-33H,9-11H2,1-4H3
InChI Key SYQOFUSBMZZRET-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H36O13
Molecular Weight 580.60 g/mol
Exact Mass 580.21559120 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 13
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[4-[2-(4-Hydroxy-3,5-dimethoxyphenyl)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-5-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6003 60.03%
Caco-2 - 0.8630 86.30%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7274 72.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8776 87.76%
OATP1B3 inhibitior + 0.9579 95.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.4788 47.88%
P-glycoprotein inhibitior + 0.5976 59.76%
P-glycoprotein substrate - 0.8228 82.28%
CYP3A4 substrate + 0.5494 54.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7587 75.87%
CYP3A4 inhibition - 0.8519 85.19%
CYP2C9 inhibition - 0.8425 84.25%
CYP2C19 inhibition - 0.7831 78.31%
CYP2D6 inhibition - 0.8849 88.49%
CYP1A2 inhibition - 0.8279 82.79%
CYP2C8 inhibition - 0.6171 61.71%
CYP inhibitory promiscuity - 0.5354 53.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6120 61.20%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9128 91.28%
Skin irritation - 0.8401 84.01%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7612 76.12%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.8200 82.00%
skin sensitisation - 0.9021 90.21%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8707 87.07%
Acute Oral Toxicity (c) III 0.6090 60.90%
Estrogen receptor binding + 0.7671 76.71%
Androgen receptor binding + 0.5452 54.52%
Thyroid receptor binding + 0.5890 58.90%
Glucocorticoid receptor binding + 0.6859 68.59%
Aromatase binding + 0.6053 60.53%
PPAR gamma + 0.6621 66.21%
Honey bee toxicity - 0.8527 85.27%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9245 92.45%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.30% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.14% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.37% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.81% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.37% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.12% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.69% 89.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.03% 89.62%
CHEMBL4208 P20618 Proteasome component C5 85.68% 90.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.26% 96.61%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.52% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.63% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.64% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.56% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.41% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.25% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.04% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.24% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.19% 92.62%

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.
Pluchea indica

Cross-Links

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PubChem 162894138
LOTUS LTS0148086
wikiData Q105263729