3-(4,6-Dihydroxy-2-methoxy-3-methylphenyl)-1-phenylpropan-1-one

Details

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Internal ID 5948f186-94a5-4214-b0ad-421233c6c5d4
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retro-dihydrochalcones
IUPAC Name 3-(4,6-dihydroxy-2-methoxy-3-methylphenyl)-1-phenylpropan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O4/c1-11-15(19)10-16(20)13(17(11)21-2)8-9-14(18)12-6-4-3-5-7-12/h3-7,10,19-20H,8-9H2,1-2H3
InChI Key FMIPTRUHEIUNEX-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) 66.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CS-0637320

2D Structure

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2D Structure of 3-(4,6-Dihydroxy-2-methoxy-3-methylphenyl)-1-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 + 0.9314 93.14%
Caco-2 + 0.7762 77.62%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.9118 91.18%
OATP2B1 inhibitior - 0.7166 71.66%
OATP1B1 inhibitior + 0.8670 86.70%
OATP1B3 inhibitior + 0.9302 93.02%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8787 87.87%
BSEP inhibitior - 0.8057 80.57%
P-glycoprotein inhibitior - 0.7795 77.95%
P-glycoprotein substrate - 0.9042 90.42%
CYP3A4 substrate - 0.5594 55.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6886 68.86%
CYP3A4 inhibition + 0.5315 53.15%
CYP2C9 inhibition + 0.6271 62.71%
CYP2C19 inhibition + 0.8331 83.31%
CYP2D6 inhibition - 0.7330 73.30%
CYP1A2 inhibition + 0.8668 86.68%
CYP2C8 inhibition + 0.7032 70.32%
CYP inhibitory promiscuity + 0.7155 71.55%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8034 80.34%
Carcinogenicity (trinary) Non-required 0.7422 74.22%
Eye corrosion - 0.9818 98.18%
Eye irritation + 0.7110 71.10%
Skin irritation - 0.7628 76.28%
Skin corrosion - 0.8942 89.42%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6266 62.66%
Micronuclear - 0.6341 63.41%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8759 87.59%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8923 89.23%
Acute Oral Toxicity (c) III 0.7460 74.60%
Estrogen receptor binding + 0.7675 76.75%
Androgen receptor binding - 0.4890 48.90%
Thyroid receptor binding - 0.5570 55.70%
Glucocorticoid receptor binding + 0.6512 65.12%
Aromatase binding + 0.5907 59.07%
PPAR gamma + 0.6625 66.25%
Honey bee toxicity - 0.9629 96.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7155 71.55%
Fish aquatic toxicity + 0.9114 91.14%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.33% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.71% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.02% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.20% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.51% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.44% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.83% 95.50%
CHEMBL4208 P20618 Proteasome component C5 85.92% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.94% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 84.12% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.94% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.78% 96.00%

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.
Calamus draco

Cross-Links

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PubChem 46869797
LOTUS LTS0183959
wikiData Q104997872