1-(2-Hydroxy-4,5-dimethoxyphenyl)-3-phenylpropan-1-one

Details

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Internal ID fd890709-33ed-4d73-a8d1-5e1db67ab72b
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxy-dihydrochalcones
IUPAC Name 1-(2-hydroxy-4,5-dimethoxyphenyl)-3-phenylpropan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O4/c1-20-16-10-13(15(19)11-17(16)21-2)14(18)9-8-12-6-4-3-5-7-12/h3-7,10-11,19H,8-9H2,1-2H3
InChI Key QNHIYZMCCPZIMU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O4
Molecular Weight 286.32 g/mol
Exact Mass 286.12050905 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2-Hydroxy-4,5-dimethoxyphenyl)-3-phenylpropan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9719 97.19%
Caco-2 + 0.8839 88.39%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.9336 93.36%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.8843 88.43%
OATP1B3 inhibitior + 0.9652 96.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.5481 54.81%
P-glycoprotein substrate - 0.7821 78.21%
CYP3A4 substrate - 0.5733 57.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7565 75.65%
CYP3A4 inhibition - 0.7068 70.68%
CYP2C9 inhibition - 0.6158 61.58%
CYP2C19 inhibition + 0.9202 92.02%
CYP2D6 inhibition - 0.7469 74.69%
CYP1A2 inhibition + 0.8775 87.75%
CYP2C8 inhibition + 0.6953 69.53%
CYP inhibitory promiscuity + 0.5684 56.84%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7654 76.54%
Carcinogenicity (trinary) Non-required 0.6865 68.65%
Eye corrosion - 0.9614 96.14%
Eye irritation + 0.8954 89.54%
Skin irritation - 0.7031 70.31%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6184 61.84%
Micronuclear - 0.6449 64.49%
Hepatotoxicity - 0.5555 55.55%
skin sensitisation - 0.9158 91.58%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7794 77.94%
Acute Oral Toxicity (c) III 0.7262 72.62%
Estrogen receptor binding + 0.7750 77.50%
Androgen receptor binding - 0.7299 72.99%
Thyroid receptor binding + 0.5384 53.84%
Glucocorticoid receptor binding + 0.6036 60.36%
Aromatase binding - 0.5616 56.16%
PPAR gamma + 0.6174 61.74%
Honey bee toxicity - 0.9157 91.57%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6649 66.49%
Fish aquatic toxicity + 0.8692 86.92%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.53% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.95% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.62% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.51% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.71% 95.50%
CHEMBL2535 P11166 Glucose transporter 92.69% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.64% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.34% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 89.19% 90.20%
CHEMBL4208 P20618 Proteasome component C5 86.93% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.96% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 80.34% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.32% 92.67%

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.
Persicaria senegalensis

Cross-Links

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PubChem 162846314
LOTUS LTS0267468
wikiData Q105224467