2-(2,5-Dimethoxyphenyl)-7-methoxychromen-4-one

Details

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Internal ID a82fa6eb-c437-482c-a7c3-a53b5ee1298e
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(2,5-dimethoxyphenyl)-7-methoxychromen-4-one
SMILES (Canonical) COC1=CC(=C(C=C1)OC)C2=CC(=O)C3=C(O2)C=C(C=C3)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)OC)C2=CC(=O)C3=C(O2)C=C(C=C3)OC
InChI InChI=1S/C18H16O5/c1-20-11-5-7-16(22-3)14(8-11)18-10-15(19)13-6-4-12(21-2)9-17(13)23-18/h4-10H,1-3H3
InChI Key FHGGYSQAPONPNP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,5-Dimethoxyphenyl)-7-methoxychromen-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 + 0.9934 99.34%
Caco-2 + 0.9478 94.78%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7189 71.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9944 99.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7539 75.39%
P-glycoprotein inhibitior + 0.9432 94.32%
P-glycoprotein substrate - 0.7255 72.55%
CYP3A4 substrate + 0.5451 54.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.5447 54.47%
CYP2C9 inhibition - 0.5560 55.60%
CYP2C19 inhibition + 0.8006 80.06%
CYP2D6 inhibition - 0.9466 94.66%
CYP1A2 inhibition + 0.9819 98.19%
CYP2C8 inhibition + 0.4790 47.90%
CYP inhibitory promiscuity + 0.8440 84.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5825 58.25%
Eye corrosion - 0.9699 96.99%
Eye irritation + 0.7850 78.50%
Skin irritation - 0.7793 77.93%
Skin corrosion - 0.9879 98.79%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3979 39.79%
Micronuclear + 0.7659 76.59%
Hepatotoxicity - 0.6060 60.60%
skin sensitisation - 0.9630 96.30%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4925 49.25%
Acute Oral Toxicity (c) II 0.4952 49.52%
Estrogen receptor binding + 0.9751 97.51%
Androgen receptor binding + 0.9322 93.22%
Thyroid receptor binding + 0.6605 66.05%
Glucocorticoid receptor binding + 0.8668 86.68%
Aromatase binding + 0.8757 87.57%
PPAR gamma + 0.7215 72.15%
Honey bee toxicity - 0.8383 83.83%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9402 94.02%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.73% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.83% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 94.41% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.11% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.73% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.39% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.59% 86.33%
CHEMBL2535 P11166 Glucose transporter 84.83% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.96% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.77% 96.77%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.58% 86.92%
CHEMBL4208 P20618 Proteasome component C5 81.58% 90.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.36% 92.38%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.64% 94.03%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.62% 95.53%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.01% 83.57%

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.
Andrographis stenophylla

Cross-Links

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PubChem 11255399
LOTUS LTS0240076
wikiData Q104995241