(2R,3R,4S,5S,6R)-2-[[2-(4-hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 5e3de1a5-5ad6-488b-928e-e3d5b3eb57a1
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name (2R,3R,4S,5S,6R)-2-[[2-(4-hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=CC2=C1OC(=C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO
SMILES (Isomeric) COC1=CC(=CC2=C1OC(=C2CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO
InChI InChI=1S/C27H34O12/c1-34-17-9-14(10-18(35-2)21(17)30)25-16(12-37-27-24(33)23(32)22(31)20(11-29)38-27)15-7-13(5-4-6-28)8-19(36-3)26(15)39-25/h7-10,20,22-24,27-33H,4-6,11-12H2,1-3H3/t20-,22-,23+,24-,27-/m1/s1
InChI Key OFYVHBYUENYMQK-UFOFBUIZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O12
Molecular Weight 550.60 g/mol
Exact Mass 550.20502652 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,5S,6R)-2-[[2-(4-hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-1-benzofuran-3-yl]methoxy]-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 + 0.5447 54.47%
Caco-2 - 0.8262 82.62%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6493 64.93%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.7720 77.20%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7243 72.43%
P-glycoprotein inhibitior - 0.4357 43.57%
P-glycoprotein substrate + 0.5769 57.69%
CYP3A4 substrate + 0.6535 65.35%
CYP2C9 substrate - 0.6202 62.02%
CYP2D6 substrate - 0.7672 76.72%
CYP3A4 inhibition - 0.9385 93.85%
CYP2C9 inhibition - 0.8482 84.82%
CYP2C19 inhibition - 0.8708 87.08%
CYP2D6 inhibition - 0.8984 89.84%
CYP1A2 inhibition - 0.8431 84.31%
CYP2C8 inhibition + 0.8342 83.42%
CYP inhibitory promiscuity - 0.7137 71.37%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5736 57.36%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9136 91.36%
Skin irritation - 0.8226 82.26%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7855 78.55%
Micronuclear - 0.5341 53.41%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.8981 89.81%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8938 89.38%
Acute Oral Toxicity (c) III 0.7076 70.76%
Estrogen receptor binding + 0.7908 79.08%
Androgen receptor binding + 0.6716 67.16%
Thyroid receptor binding + 0.5469 54.69%
Glucocorticoid receptor binding + 0.7489 74.89%
Aromatase binding + 0.5988 59.88%
PPAR gamma + 0.5717 57.17%
Honey bee toxicity - 0.7290 72.90%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.4925 49.25%

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 99.27% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.12% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.09% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.25% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.63% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.68% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.56% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.55% 86.33%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.37% 97.36%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.29% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.09% 92.94%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.52% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.83% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.44% 92.62%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.69% 94.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.98% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.88% 91.71%
CHEMBL5555 O00767 Acyl-CoA desaturase 81.17% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 80.22% 94.73%

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.
Selaginella moellendorffii

Cross-Links

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PubChem 102262568
LOTUS LTS0016555
wikiData Q105191467