5,7-Dihydroxy-3,6-dimethoxy-2-(4-methoxy-3-methylphenyl)chromen-4-one

Details

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Internal ID e0d8954c-2f6e-4872-860c-bfdef32c8887
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 5,7-dihydroxy-3,6-dimethoxy-2-(4-methoxy-3-methylphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O7/c1-9-7-10(5-6-12(9)23-2)17-19(25-4)16(22)14-13(26-17)8-11(20)18(24-3)15(14)21/h5-8,20-21H,1-4H3
InChI Key ILZWKKZNJFLJKJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O7
Molecular Weight 358.30 g/mol
Exact Mass 358.10525291 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,7-Dihydroxy-3,6-dimethoxy-2-(4-methoxy-3-methylphenyl)chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9417 94.17%
Caco-2 + 0.8015 80.15%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6343 63.43%
OATP2B1 inhibitior - 0.7107 71.07%
OATP1B1 inhibitior + 0.9576 95.76%
OATP1B3 inhibitior + 0.8767 87.67%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6192 61.92%
P-glycoprotein inhibitior + 0.7542 75.42%
P-glycoprotein substrate - 0.8319 83.19%
CYP3A4 substrate + 0.5634 56.34%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.6154 61.54%
CYP2C9 inhibition - 0.7484 74.84%
CYP2C19 inhibition + 0.5640 56.40%
CYP2D6 inhibition - 0.7310 73.10%
CYP1A2 inhibition + 0.8610 86.10%
CYP2C8 inhibition + 0.8581 85.81%
CYP inhibitory promiscuity + 0.8068 80.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6142 61.42%
Eye corrosion - 0.9818 98.18%
Eye irritation - 0.4771 47.71%
Skin irritation - 0.7187 71.87%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4758 47.58%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8523 85.23%
Acute Oral Toxicity (c) III 0.5210 52.10%
Estrogen receptor binding + 0.9294 92.94%
Androgen receptor binding + 0.7533 75.33%
Thyroid receptor binding + 0.6760 67.60%
Glucocorticoid receptor binding + 0.8430 84.30%
Aromatase binding + 0.7737 77.37%
PPAR gamma + 0.8597 85.97%
Honey bee toxicity - 0.8811 88.11%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8724 87.24%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.58% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.02% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.38% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.65% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.30% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.05% 99.15%
CHEMBL2581 P07339 Cathepsin D 90.59% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.27% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.74% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.50% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.36% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.15% 99.23%
CHEMBL3194 P02766 Transthyretin 84.40% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 83.91% 94.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.73% 95.78%
CHEMBL1255126 O15151 Protein Mdm4 82.92% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.17% 99.17%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.76% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.94% 96.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.87% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.65% 95.50%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.20% 85.00%

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.
Achillea multifida

Cross-Links

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PubChem 162923782
LOTUS LTS0231448
wikiData Q105115561