2-(3,4-Dimethoxy-5-methylphenyl)-3,5,7-trihydroxychromen-4-one

Details

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Internal ID fa23c165-e552-4698-a384-2511f0232a8c
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 2-(3,4-dimethoxy-5-methylphenyl)-3,5,7-trihydroxychromen-4-one
SMILES (Canonical) CC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
SMILES (Isomeric) CC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
InChI InChI=1S/C18H16O7/c1-8-4-9(5-13(23-2)17(8)24-3)18-16(22)15(21)14-11(20)6-10(19)7-12(14)25-18/h4-7,19-20,22H,1-3H3
InChI Key XIYDXXMVCUQISU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,4-Dimethoxy-5-methylphenyl)-3,5,7-trihydroxychromen-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 + 0.7036 70.36%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6343 63.43%
OATP2B1 inhibitior - 0.6891 68.91%
OATP1B1 inhibitior + 0.8848 88.48%
OATP1B3 inhibitior + 0.8767 87.67%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7221 72.21%
P-glycoprotein inhibitior + 0.7207 72.07%
P-glycoprotein substrate - 0.6773 67.73%
CYP3A4 substrate + 0.6058 60.58%
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 + 0.9167 91.67%
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 + 0.6319 63.19%
Skin irritation - 0.7187 71.87%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4561 45.61%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8054 80.54%
Acute Oral Toxicity (c) III 0.5210 52.10%
Estrogen receptor binding + 0.9205 92.05%
Androgen receptor binding + 0.6042 60.42%
Thyroid receptor binding + 0.6575 65.75%
Glucocorticoid receptor binding + 0.8523 85.23%
Aromatase binding + 0.7960 79.60%
PPAR gamma + 0.8648 86.48%
Honey bee toxicity - 0.8735 87.35%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5500 55.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.13% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.22% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.11% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.04% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.99% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.69% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 89.63% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.46% 96.12%
CHEMBL3194 P02766 Transthyretin 89.32% 90.71%
CHEMBL2581 P07339 Cathepsin D 89.02% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.80% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.61% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.53% 93.65%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.35% 98.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.24% 95.50%
CHEMBL4208 P20618 Proteasome component C5 81.98% 90.00%
CHEMBL2424 Q04760 Glyoxalase I 81.94% 91.67%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.46% 94.42%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.34% 95.64%

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.
Haplopappus integerrimus

Cross-Links

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PubChem 162969651
LOTUS LTS0156578
wikiData Q105328796