(2R,3S)-5-methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-6-ol

Details

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Internal ID 62fd9444-5252-446a-b36b-08d41fcdcb68
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name (2R,3S)-5-methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O6/c1-7-8-14-19(23)16(24-3)11-15-12(2)20(28-21(14)15)13-9-17(25-4)22(27-6)18(10-13)26-5/h7,9-12,20,23H,1,8H2,2-6H3/t12-,20+/m0/s1
InChI Key AJYMYDPCSNAOAB-FKIZINRSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O6
Molecular Weight 386.40 g/mol
Exact Mass 386.17293854 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S)-5-methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.7601 76.01%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6165 61.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7740 77.40%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7669 76.69%
P-glycoprotein inhibitior + 0.7226 72.26%
P-glycoprotein substrate - 0.8082 80.82%
CYP3A4 substrate + 0.5641 56.41%
CYP2C9 substrate - 0.6036 60.36%
CYP2D6 substrate + 0.4888 48.88%
CYP3A4 inhibition + 0.6903 69.03%
CYP2C9 inhibition + 0.5747 57.47%
CYP2C19 inhibition + 0.8261 82.61%
CYP2D6 inhibition - 0.8509 85.09%
CYP1A2 inhibition + 0.6721 67.21%
CYP2C8 inhibition + 0.8065 80.65%
CYP inhibitory promiscuity + 0.9282 92.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.4055 40.55%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.7239 72.39%
Skin irritation - 0.7929 79.29%
Skin corrosion - 0.9487 94.87%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8007 80.07%
Micronuclear + 0.7418 74.18%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7671 76.71%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.9208 92.08%
Acute Oral Toxicity (c) II 0.4974 49.74%
Estrogen receptor binding + 0.8244 82.44%
Androgen receptor binding + 0.5353 53.53%
Thyroid receptor binding + 0.7989 79.89%
Glucocorticoid receptor binding + 0.6849 68.49%
Aromatase binding + 0.5315 53.15%
PPAR gamma + 0.6296 62.96%
Honey bee toxicity - 0.7583 75.83%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9890 98.90%

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 99.13% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.66% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.48% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.24% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.33% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.75% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.09% 89.00%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 81.99% 89.32%
CHEMBL3401 O75469 Pregnane X receptor 81.77% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.75% 92.62%

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 162820353
LOTUS LTS0215622
wikiData Q104913470