2,5-Dimethylstyrene

Details

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Internal ID 632299ee-ed02-4b60-85a8-ecfe22797dd4
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 2-ethenyl-1,4-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/c1-4-10-7-8(2)5-6-9(10)3/h4-7H,1H2,2-3H3
InChI Key DBWWINQJTZYDFK-UHFFFAOYSA-N
Popularity 33 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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2039-89-6
1,4-Dimethyl-2-vinylbenzene
Benzene, 2-ethenyl-1,4-dimethyl-
Styrene, 2,5-dimethyl-
2-ethenyl-1,4-dimethylbenzene
1,4-Dimethyl-2-ethenylbenzene
EINECS 218-028-9
UNII-RTM6P5K8CA
NSC 73477
RTM6P5K8CA
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,5-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 + 0.9626 96.26%
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 + 0.9397 93.97%
OATP1B3 inhibitior + 0.9653 96.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8760 87.60%
P-glycoprotein inhibitior - 0.9735 97.35%
P-glycoprotein substrate - 0.9786 97.86%
CYP3A4 substrate - 0.7351 73.51%
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 - 0.9171 91.71%
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 + 1.0000 100.00%
Skin irritation + 0.8924 89.24%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6852 68.52%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.9809 98.09%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5769 57.69%
Acute Oral Toxicity (c) III 0.8037 80.37%
Estrogen receptor binding - 0.8841 88.41%
Androgen receptor binding - 0.8632 86.32%
Thyroid receptor binding - 0.8119 81.19%
Glucocorticoid receptor binding - 0.9336 93.36%
Aromatase binding - 0.7833 78.33%
PPAR gamma - 0.8893 88.93%
Honey bee toxicity - 0.9493 94.93%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6400 64.00%
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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.14% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.92% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.81% 94.73%
CHEMBL2039 P27338 Monoamine oxidase B 85.79% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.32% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.27% 96.00%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.07% 90.93%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.72% 81.29%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.27% 86.00%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 80.24% 83.14%

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.
Thymus quinquecostatus
Thymus vulgaris

Cross-Links

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PubChem 16265
NPASS NPC143292