3-Ethoxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one

Details

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Internal ID 769fc001-9c04-4df1-88ff-8fa7ae8cb7fc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 3-ethoxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one
SMILES (Canonical) CCOCCC(=O)C1=CC(=C(C=C1)O)OC
SMILES (Isomeric) CCOCCC(=O)C1=CC(=C(C=C1)O)OC
InChI InChI=1S/C12H16O4/c1-3-16-7-6-10(13)9-4-5-11(14)12(8-9)15-2/h4-5,8,14H,3,6-7H2,1-2H3
InChI Key FZNMZQOIQMBXQC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.70
Atomic LogP (AlogP) 2.01
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 3-Ethoxy-1-(4-hydroxy-3-methoxyphenyl)propan-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 + 0.9930 99.30%
Caco-2 + 0.9245 92.45%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.9121 91.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7826 78.26%
P-glycoprotein inhibitior - 0.9690 96.90%
P-glycoprotein substrate - 0.8939 89.39%
CYP3A4 substrate - 0.5686 56.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7071 70.71%
CYP3A4 inhibition - 0.8638 86.38%
CYP2C9 inhibition - 0.8697 86.97%
CYP2C19 inhibition - 0.5317 53.17%
CYP2D6 inhibition - 0.8739 87.39%
CYP1A2 inhibition - 0.6314 63.14%
CYP2C8 inhibition + 0.7048 70.48%
CYP inhibitory promiscuity - 0.8717 87.17%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7943 79.43%
Carcinogenicity (trinary) Non-required 0.6705 67.05%
Eye corrosion - 0.9749 97.49%
Eye irritation + 0.9688 96.88%
Skin irritation - 0.7552 75.52%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6651 66.51%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6080 60.80%
skin sensitisation - 0.6090 60.90%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6186 61.86%
Acute Oral Toxicity (c) III 0.8191 81.91%
Estrogen receptor binding + 0.7147 71.47%
Androgen receptor binding - 0.7756 77.56%
Thyroid receptor binding - 0.7569 75.69%
Glucocorticoid receptor binding - 0.6405 64.05%
Aromatase binding - 0.5799 57.99%
PPAR gamma - 0.6144 61.44%
Honey bee toxicity - 0.9388 93.88%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6715 67.15%
Fish aquatic toxicity + 0.8316 83.16%

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 95.22% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.90% 99.17%
CHEMBL4208 P20618 Proteasome component C5 93.36% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.56% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.69% 86.33%
CHEMBL2535 P11166 Glucose transporter 88.54% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.34% 90.24%
CHEMBL1255126 O15151 Protein Mdm4 86.29% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.01% 96.95%
CHEMBL3194 P02766 Transthyretin 82.62% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.28% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.00% 95.56%

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.
Diospyros maritima

Cross-Links

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PubChem 100956074
LOTUS LTS0275210
wikiData Q105005061