2-(4-Hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-4-methyl-1-benzofuran-3,7-diol

Details

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Internal ID 96a2219e-9f41-4fa9-b673-88dbd7a97d55
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-4-methyl-1-benzofuran-3,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20O6/c1-10-11(4-3-7-20)8-14(22)19-16(10)17(23)18(25-19)12-5-6-13(21)15(9-12)24-2/h5-6,8-9,20-23H,3-4,7H2,1-2H3
InChI Key GXIZPXUKIGHETN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O6
Molecular Weight 344.40 g/mol
Exact Mass 344.12598835 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4-Hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-4-methyl-1-benzofuran-3,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 - 0.5628 56.28%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7504 75.04%
OATP2B1 inhibitior + 0.5794 57.94%
OATP1B1 inhibitior + 0.8699 86.99%
OATP1B3 inhibitior + 0.9224 92.24%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6609 66.09%
P-glycoprotein inhibitior - 0.6203 62.03%
P-glycoprotein substrate - 0.6395 63.95%
CYP3A4 substrate + 0.5701 57.01%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate + 0.4027 40.27%
CYP3A4 inhibition - 0.6287 62.87%
CYP2C9 inhibition - 0.5757 57.57%
CYP2C19 inhibition - 0.6524 65.24%
CYP2D6 inhibition - 0.8850 88.50%
CYP1A2 inhibition + 0.6326 63.26%
CYP2C8 inhibition + 0.9012 90.12%
CYP inhibitory promiscuity + 0.6450 64.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6013 60.13%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.5962 59.62%
Skin irritation - 0.7640 76.40%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis + 0.5272 52.72%
Human Ether-a-go-go-Related Gene inhibition + 0.7163 71.63%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8694 86.94%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8267 82.67%
Acute Oral Toxicity (c) III 0.5321 53.21%
Estrogen receptor binding + 0.9204 92.04%
Androgen receptor binding + 0.6912 69.12%
Thyroid receptor binding + 0.6744 67.44%
Glucocorticoid receptor binding + 0.9243 92.43%
Aromatase binding + 0.8225 82.25%
PPAR gamma + 0.8513 85.13%
Honey bee toxicity - 0.8951 89.51%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7825 78.25%

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 99.11% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.10% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.45% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 93.79% 98.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.86% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.77% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.01% 98.95%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 89.59% 95.48%
CHEMBL3401 O75469 Pregnane X receptor 89.12% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.62% 86.92%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.48% 95.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.44% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.39% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.25% 89.00%
CHEMBL3194 P02766 Transthyretin 85.65% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.56% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.38% 95.50%
CHEMBL1907 P15144 Aminopeptidase N 83.63% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.52% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.38% 91.71%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.78% 90.24%
CHEMBL3438 Q05513 Protein kinase C zeta 81.57% 88.48%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.59% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.29% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.25% 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.
Pinus sibirica

Cross-Links

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PubChem 163192263
LOTUS LTS0152891
wikiData Q105023089