1-(2-Hydroxy-3-methoxy-5-prop-1-enylphenyl)ethanone

Details

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Internal ID 102973bb-8280-417d-bbca-b67aedde94ed
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2-hydroxy-3-methoxy-5-prop-1-enylphenyl)ethanone
SMILES (Canonical) CC=CC1=CC(=C(C(=C1)OC)O)C(=O)C
SMILES (Isomeric) CC=CC1=CC(=C(C(=C1)OC)O)C(=O)C
InChI InChI=1S/C12H14O3/c1-4-5-9-6-10(8(2)13)12(14)11(7-9)15-3/h4-7,14H,1-3H3
InChI Key QYXQLUHJDINRRQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O3
Molecular Weight 206.24 g/mol
Exact Mass 206.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2-Hydroxy-3-methoxy-5-prop-1-enylphenyl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7140 71.40%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8396 83.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8760 87.60%
OATP1B3 inhibitior + 0.9814 98.14%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6334 63.34%
P-glycoprotein inhibitior - 0.9563 95.63%
P-glycoprotein substrate - 0.8568 85.68%
CYP3A4 substrate - 0.5991 59.91%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.8304 83.04%
CYP3A4 inhibition - 0.8046 80.46%
CYP2C9 inhibition - 0.9900 99.00%
CYP2C19 inhibition - 0.7570 75.70%
CYP2D6 inhibition - 0.9385 93.85%
CYP1A2 inhibition - 0.6316 63.16%
CYP2C8 inhibition - 0.5718 57.18%
CYP inhibitory promiscuity - 0.7009 70.09%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7825 78.25%
Carcinogenicity (trinary) Non-required 0.6144 61.44%
Eye corrosion + 0.6814 68.14%
Eye irritation + 0.9307 93.07%
Skin irritation + 0.7100 71.00%
Skin corrosion - 0.9521 95.21%
Ames mutagenesis - 0.7778 77.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6494 64.94%
Micronuclear + 0.5133 51.33%
Hepatotoxicity + 0.5930 59.30%
skin sensitisation - 0.6964 69.64%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6168 61.68%
Acute Oral Toxicity (c) III 0.8445 84.45%
Estrogen receptor binding - 0.6221 62.21%
Androgen receptor binding - 0.7177 71.77%
Thyroid receptor binding - 0.5553 55.53%
Glucocorticoid receptor binding - 0.6996 69.96%
Aromatase binding - 0.6697 66.97%
PPAR gamma - 0.5631 56.31%
Honey bee toxicity - 0.8143 81.43%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9134 91.34%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.05% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.77% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.67% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.00% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.88% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.56% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.44% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 84.26% 94.73%
CHEMBL2535 P11166 Glucose transporter 83.72% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.20% 89.00%
CHEMBL3788 O00444 Serine/threonine-protein kinase PLK4 82.13% 83.65%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.48% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.77% 99.17%

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.
Artemisia capillaris

Cross-Links

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PubChem 86079729
LOTUS LTS0151493
wikiData Q105231136