1,2-Dimethoxy-4-(prop-1-en-2-yl)benzene

Details

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Internal ID 33cbd735-cf8c-4347-81ee-cb78e9623301
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 1,2-dimethoxy-4-prop-1-en-2-ylbenzene
SMILES (Canonical) CC(=C)C1=CC(=C(C=C1)OC)OC
SMILES (Isomeric) CC(=C)C1=CC(=C(C=C1)OC)OC
InChI InChI=1S/C11H14O2/c1-8(2)9-5-6-10(12-3)11(7-9)13-4/h5-7H,1H2,2-4H3
InChI Key PRHTXAOWJQTLBO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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30405-75-5
1,2-dimethoxy-4-prop-1-en-2-ylbenzene
Benzene, 1,2-dimethoxy-4-(1-methylethenyl)-
SCHEMBL8296526
DTXSID60515448
AKOS013990775
EN300-180310
Z1238836374

2D Structure

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2D Structure of 1,2-Dimethoxy-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 + 0.9970 99.70%
Caco-2 + 0.8885 88.85%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6916 69.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8622 86.22%
P-glycoprotein inhibitior - 0.9626 96.26%
P-glycoprotein substrate - 0.8516 85.16%
CYP3A4 substrate - 0.6691 66.91%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.6632 66.32%
CYP3A4 inhibition - 0.6074 60.74%
CYP2C9 inhibition - 0.9395 93.95%
CYP2C19 inhibition + 0.5434 54.34%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition + 0.6175 61.75%
CYP2C8 inhibition + 0.5079 50.79%
CYP inhibitory promiscuity + 0.7165 71.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7109 71.09%
Carcinogenicity (trinary) Non-required 0.5456 54.56%
Eye corrosion - 0.6925 69.25%
Eye irritation + 0.9872 98.72%
Skin irritation - 0.5578 55.78%
Skin corrosion - 0.9460 94.60%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4425 44.25%
Micronuclear - 0.7867 78.67%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation + 0.7214 72.14%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5118 51.18%
Acute Oral Toxicity (c) III 0.8223 82.23%
Estrogen receptor binding - 0.7944 79.44%
Androgen receptor binding - 0.8031 80.31%
Thyroid receptor binding - 0.7074 70.74%
Glucocorticoid receptor binding - 0.9201 92.01%
Aromatase binding - 0.6700 67.00%
PPAR gamma - 0.7837 78.37%
Honey bee toxicity - 0.9311 93.11%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5551 55.51%
Fish aquatic toxicity + 0.9646 96.46%

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 93.09% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 90.59% 90.20%
CHEMBL4208 P20618 Proteasome component C5 88.89% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.73% 96.09%
CHEMBL2535 P11166 Glucose transporter 86.98% 98.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.91% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.70% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.30% 93.99%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.13% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.30% 91.11%

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.
Laurus nobilis
Pinus densiflora

Cross-Links

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PubChem 13022452
LOTUS LTS0152957
wikiData Q82376329