5-Methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-1-benzofuran-6-ol

Details

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Internal ID 3360e0d6-2c7e-472c-ba19-fc58f847632d
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 5-methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-1-benzofuran-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O6/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/h7,9-11,23H,1,8H2,2-6H3
InChI Key DGKDCYBFRAMIID-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 70.30 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.88
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 5-Methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-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 + 0.7054 70.54%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6165 61.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8049 80.49%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6877 68.77%
P-glycoprotein inhibitior + 0.8094 80.94%
P-glycoprotein substrate - 0.6830 68.30%
CYP3A4 substrate + 0.5424 54.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4182 41.82%
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 + 0.8844 88.44%
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 - 0.6439 64.39%
Skin irritation - 0.7929 79.29%
Skin corrosion - 0.9487 94.87%
Ames mutagenesis + 0.5146 51.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8185 81.85%
Micronuclear + 0.7418 74.18%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.7671 76.71%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8969 89.69%
Acute Oral Toxicity (c) II 0.4974 49.74%
Estrogen receptor binding + 0.8786 87.86%
Androgen receptor binding + 0.5757 57.57%
Thyroid receptor binding + 0.7759 77.59%
Glucocorticoid receptor binding + 0.7949 79.49%
Aromatase binding + 0.7087 70.87%
PPAR gamma + 0.7783 77.83%
Honey bee toxicity - 0.8035 80.35%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
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 97.91% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 90.81% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.01% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.98% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.80% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.12% 83.57%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.59% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.97% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.58% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.58% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.94% 92.62%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.39% 97.21%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.73% 95.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.65% 96.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.32% 92.94%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.16% 95.50%

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.
Rhodostemonodaphne miranda

Cross-Links

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PubChem 162848980
LOTUS LTS0191368
wikiData Q104166396