5-Hydroxy-6-methoxy-7-methyl-2-(4-methylphenyl)chromen-4-one

Details

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Internal ID 53ddbd81-8082-43b3-8a4a-84c0fca83a72
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 5-hydroxy-6-methoxy-7-methyl-2-(4-methylphenyl)chromen-4-one
SMILES (Canonical) CC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)C
SMILES (Isomeric) CC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)C
InChI InChI=1S/C18H16O4/c1-10-4-6-12(7-5-10)14-9-13(19)16-15(22-14)8-11(2)18(21-3)17(16)20/h4-9,20H,1-3H3
InChI Key ZZPHAQJIENBZOF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O4
Molecular Weight 296.30 g/mol
Exact Mass 296.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.79
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-6-methoxy-7-methyl-2-(4-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 + 0.9823 98.23%
Caco-2 + 0.7870 78.70%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.9817 98.17%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6616 66.16%
P-glycoprotein inhibitior + 0.8614 86.14%
P-glycoprotein substrate - 0.9357 93.57%
CYP3A4 substrate + 0.5300 53.00%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
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 + 0.5672 56.72%
CYP inhibitory promiscuity + 0.6103 61.03%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5716 57.16%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.5483 54.83%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4069 40.69%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9504 95.04%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8695 86.95%
Acute Oral Toxicity (c) II 0.4982 49.82%
Estrogen receptor binding + 0.9356 93.56%
Androgen receptor binding + 0.8481 84.81%
Thyroid receptor binding + 0.7045 70.45%
Glucocorticoid receptor binding + 0.7995 79.95%
Aromatase binding + 0.8155 81.55%
PPAR gamma + 0.8818 88.18%
Honey bee toxicity - 0.8867 88.67%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8902 89.02%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.73% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.91% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.25% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.74% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.11% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.49% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.35% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.16% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.20% 99.15%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.52% 81.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.14% 94.45%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.10% 95.78%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.62% 93.65%
CHEMBL3194 P02766 Transthyretin 81.76% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.54% 99.23%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.28% 97.28%

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.
Arnica acaulis

Cross-Links

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PubChem 162948092
LOTUS LTS0109366
wikiData Q105386963