2-(4-Hydroxy-3-methoxyphenyl)-6,7-dimethoxychromen-4-one

Details

Top
Internal ID aee50730-500b-44ef-a396-090f86e3f368
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxychromen-4-one
SMILES (Canonical) COC1=C(C=CC(=C1)C2=CC(=O)C3=CC(=C(C=C3O2)OC)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=CC(=O)C3=CC(=C(C=C3O2)OC)OC)O
InChI InChI=1S/C18H16O6/c1-21-16-6-10(4-5-12(16)19)14-8-13(20)11-7-17(22-2)18(23-3)9-15(11)24-14/h4-9,19H,1-3H3
InChI Key YPSSIDWEZCIQGA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(4-Hydroxy-3-methoxyphenyl)-6,7-dimethoxychromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.8762 87.62%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 0.7278 72.78%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9817 98.17%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5699 56.99%
P-glycoprotein inhibitior + 0.7953 79.53%
P-glycoprotein substrate - 0.8207 82.07%
CYP3A4 substrate - 0.5194 51.94%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition - 0.5748 57.48%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition + 0.5778 57.78%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.8530 85.30%
CYP2C8 inhibition + 0.7041 70.41%
CYP inhibitory promiscuity + 0.6103 61.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5716 57.16%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.6185 61.85%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7665 76.65%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.9504 95.04%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8046 80.46%
Acute Oral Toxicity (c) II 0.4982 49.82%
Estrogen receptor binding + 0.9404 94.04%
Androgen receptor binding + 0.8245 82.45%
Thyroid receptor binding + 0.6442 64.42%
Glucocorticoid receptor binding + 0.8524 85.24%
Aromatase binding + 0.6534 65.34%
PPAR gamma + 0.7625 76.25%
Honey bee toxicity - 0.8896 88.96%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity + 0.8902 89.02%

Targets

Top

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 97.97% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.88% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.92% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.72% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.88% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.77% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.30% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.23% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 87.37% 98.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.96% 92.94%
CHEMBL1907 P15144 Aminopeptidase N 86.06% 93.31%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.62% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.72% 86.92%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.42% 99.23%
CHEMBL3194 P02766 Transthyretin 81.30% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.33% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.29% 94.45%

Plants that contains it

Top
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.
Artemisia annua
Artemisia capillaris
Thymus vulgaris

Cross-Links

Top
PubChem 14235159
NPASS NPC20830