2,4-Dimethylstyrene

Details

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Internal ID b408ef67-ef46-4884-9735-6bae8ff81388
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 1-ethenyl-2,4-dimethylbenzene
SMILES (Canonical) CC1=CC(=C(C=C1)C=C)C
SMILES (Isomeric) CC1=CC(=C(C=C1)C=C)C
InChI InChI=1S/C10H12/c1-4-10-6-5-8(2)7-9(10)3/h4-7H,1H2,2-3H3
InChI Key OEVVKKAVYQFQNV-UHFFFAOYSA-N
Popularity 42 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12
Molecular Weight 132.20 g/mol
Exact Mass 132.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2,4-Dimethyl-1-vinylbenzene
4-Vinyl-m-xylene
1-ethenyl-2,4-dimethylbenzene
1,3-Dimethyl-4-vinylbenzene
1-Vinyl-2,4-dimethylbenzene
Styrene, 2,4-dimethyl-
Benzene, 1-ethenyl-2,4-dimethyl-
1,3-Dimethyl-4-ethenylbenzene
EINECS 218-781-3
NSC 62089
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4-Dimethylstyrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.9448 94.48%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.4917 49.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9653 96.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8651 86.51%
P-glycoprotein inhibitior - 0.9811 98.11%
P-glycoprotein substrate - 0.9814 98.14%
CYP3A4 substrate - 0.7495 74.95%
CYP2C9 substrate - 0.7067 70.67%
CYP2D6 substrate - 0.7432 74.32%
CYP3A4 inhibition - 0.8865 88.65%
CYP2C9 inhibition - 0.8707 87.07%
CYP2C19 inhibition - 0.6666 66.66%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.5845 58.45%
CYP2C8 inhibition - 0.9017 90.17%
CYP inhibitory promiscuity - 0.5338 53.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.4788 47.88%
Eye corrosion + 0.9777 97.77%
Eye irritation + 0.9954 99.54%
Skin irritation + 0.8924 89.24%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6569 65.69%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.9809 98.09%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.7041 70.41%
Acute Oral Toxicity (c) III 0.8037 80.37%
Estrogen receptor binding - 0.8834 88.34%
Androgen receptor binding - 0.7931 79.31%
Thyroid receptor binding - 0.8181 81.81%
Glucocorticoid receptor binding - 0.9405 94.05%
Aromatase binding - 0.8269 82.69%
PPAR gamma - 0.8598 85.98%
Honey bee toxicity - 0.9493 94.93%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9932 99.32%

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
CHEMBL2039 P27338 Monoamine oxidase B 93.47% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.01% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.49% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.75% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.09% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.30% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.55% 86.33%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.89% 97.36%
CHEMBL1951 P21397 Monoamine oxidase A 80.47% 91.49%

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.
Hansenia forbesii
Hansenia weberbaueriana

Cross-Links

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PubChem 16694
NPASS NPC22338