2,4-Dimethoxy-1-prop-1-enylbenzene

Details

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Internal ID 5796453d-ba65-45da-a2e5-ca687cb562d2
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 2,4-dimethoxy-1-prop-1-enylbenzene
SMILES (Canonical) CC=CC1=C(C=C(C=C1)OC)OC
SMILES (Isomeric) CC=CC1=C(C=C(C=C1)OC)OC
InChI InChI=1S/C11H14O2/c1-4-5-9-6-7-10(12-2)8-11(9)13-3/h4-8H,1-3H3
InChI Key SKWTXGMULLCOGN-UHFFFAOYSA-N
Popularity 2 references 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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SCHEMBL3172829

2D Structure

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2D Structure of 2,4-Dimethoxy-1-prop-1-enylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8817 88.17%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7856 78.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior + 0.9879 98.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7617 76.17%
P-glycoprotein inhibitior - 0.9716 97.16%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate - 0.6267 62.67%
CYP2C9 substrate + 0.6036 60.36%
CYP2D6 substrate - 0.6859 68.59%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.9821 98.21%
CYP2C19 inhibition - 0.8024 80.24%
CYP2D6 inhibition - 0.9510 95.10%
CYP1A2 inhibition + 0.7076 70.76%
CYP2C8 inhibition - 0.6042 60.42%
CYP inhibitory promiscuity + 0.6454 64.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6533 65.33%
Carcinogenicity (trinary) Non-required 0.5508 55.08%
Eye corrosion + 0.7466 74.66%
Eye irritation + 0.9837 98.37%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9203 92.03%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4046 40.46%
Micronuclear - 0.7667 76.67%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.7434 74.34%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5682 56.82%
Acute Oral Toxicity (c) III 0.7727 77.27%
Estrogen receptor binding - 0.7140 71.40%
Androgen receptor binding - 0.6865 68.65%
Thyroid receptor binding - 0.7937 79.37%
Glucocorticoid receptor binding - 0.8635 86.35%
Aromatase binding - 0.7648 76.48%
PPAR gamma - 0.8727 87.27%
Honey bee toxicity - 0.9194 91.94%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8900 89.00%
Fish aquatic toxicity + 0.9043 90.43%

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 95.47% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.92% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 94.28% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.21% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.03% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.26% 97.36%
CHEMBL4208 P20618 Proteasome component C5 89.21% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.43% 90.24%
CHEMBL2535 P11166 Glucose transporter 84.86% 98.75%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 84.05% 89.32%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.11% 99.17%
CHEMBL2487 P05067 Beta amyloid A4 protein 80.68% 96.74%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.44% 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.
Osmorhiza aristata

Cross-Links

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PubChem 3013948
LOTUS LTS0224958
wikiData Q105255085