2-Methoxy-1-methyl-4-(prop-1-en-2-yl)benzene

Details

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Internal ID d15633ff-c0df-48e5-9e51-7be179179fe7
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropenes
IUPAC Name 2-methoxy-1-methyl-4-prop-1-en-2-ylbenzene
SMILES (Canonical) CC1=C(C=C(C=C1)C(=C)C)OC
SMILES (Isomeric) CC1=C(C=C(C=C1)C(=C)C)OC
InChI InChI=1S/C11H14O/c1-8(2)10-6-5-9(3)11(7-10)12-4/h5-7H,1H2,2-4H3
InChI Key SHZSFIUMTQEXDN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O
Molecular Weight 162.23 g/mol
Exact Mass 162.104465066 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-methoxy-1-methyl-4-(prop-1-en-2-yl)benzene
SCHEMBL11611523
DTXSID40628343

2D Structure

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2D Structure of 2-Methoxy-1-methyl-4-(prop-1-en-2-yl)benzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8836 88.36%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6518 65.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9725 97.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8666 86.66%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.8942 89.42%
CYP3A4 substrate - 0.6358 63.58%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.6632 66.32%
CYP3A4 inhibition - 0.6670 66.70%
CYP2C9 inhibition - 0.9275 92.75%
CYP2C19 inhibition + 0.5315 53.15%
CYP2D6 inhibition - 0.9204 92.04%
CYP1A2 inhibition + 0.7596 75.96%
CYP2C8 inhibition + 0.5514 55.14%
CYP inhibitory promiscuity + 0.7494 74.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6331 63.31%
Carcinogenicity (trinary) Non-required 0.5729 57.29%
Eye corrosion + 0.4625 46.25%
Eye irritation + 0.9927 99.27%
Skin irritation - 0.5951 59.51%
Skin corrosion - 0.9113 91.13%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5441 54.41%
Micronuclear - 0.8541 85.41%
Hepatotoxicity - 0.5685 56.85%
skin sensitisation + 0.7735 77.35%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.5577 55.77%
Acute Oral Toxicity (c) III 0.8312 83.12%
Estrogen receptor binding - 0.8159 81.59%
Androgen receptor binding - 0.8802 88.02%
Thyroid receptor binding - 0.7858 78.58%
Glucocorticoid receptor binding - 0.9399 93.99%
Aromatase binding - 0.7125 71.25%
PPAR gamma - 0.8013 80.13%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9806 98.06%

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 92.52% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.30% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.48% 97.21%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.26% 89.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.84% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.83% 91.11%
CHEMBL2535 P11166 Glucose transporter 83.91% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.44% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 82.07% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.31% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.97% 93.99%

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.
Linaria saxatilis

Cross-Links

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PubChem 22768675
LOTUS LTS0010309
wikiData Q104986900