o-Isopropenyltoluene

Details

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Internal ID dac2daa9-2631-40f8-b331-c1431330a541
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropenes
IUPAC Name 1-methyl-2-prop-1-en-2-ylbenzene
SMILES (Canonical) CC1=CC=CC=C1C(=C)C
SMILES (Isomeric) CC1=CC=CC=C1C(=C)C
InChI InChI=1S/C10H12/c1-8(2)10-7-5-4-6-9(10)3/h4-7H,1H2,2-3H3
InChI Key OGMSGZZPTQNTIK-UHFFFAOYSA-N
Popularity 24 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 3.70
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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o-Isopropenyltoluene
7399-49-7
1-Methyl-2-(prop-1-en-2-yl)benzene
26444-18-8
o,alpha-Dimethylstyrene
Benzene, methyl(1-methylethenyl)-
alpha,2-Dimethylstyrene
isopropenyltoluene
1-methyl-2-prop-1-en-2-ylbenzene
1-Isopropenyl-2-methylbenzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of o-Isopropenyltoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.9575 95.75%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4786 47.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8979 89.79%
P-glycoprotein inhibitior - 0.9864 98.64%
P-glycoprotein substrate - 0.9624 96.24%
CYP3A4 substrate - 0.7437 74.37%
CYP2C9 substrate - 0.7067 70.67%
CYP2D6 substrate - 0.7432 74.32%
CYP3A4 inhibition - 0.8374 83.74%
CYP2C9 inhibition - 0.8355 83.55%
CYP2C19 inhibition - 0.5172 51.72%
CYP2D6 inhibition - 0.8352 83.52%
CYP1A2 inhibition - 0.5184 51.84%
CYP2C8 inhibition - 0.8624 86.24%
CYP inhibitory promiscuity + 0.6854 68.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5077 50.77%
Eye corrosion + 0.8876 88.76%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8145 81.45%
Skin corrosion - 0.9546 95.46%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6841 68.41%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation + 0.9767 97.67%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6023 60.23%
Acute Oral Toxicity (c) III 0.8000 80.00%
Estrogen receptor binding - 0.9411 94.11%
Androgen receptor binding - 0.9284 92.84%
Thyroid receptor binding - 0.8316 83.16%
Glucocorticoid receptor binding - 0.9143 91.43%
Aromatase binding - 0.8690 86.90%
PPAR gamma - 0.8538 85.38%
Honey bee toxicity - 0.9666 96.66%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9956 99.56%

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 88.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.36% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.34% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.26% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.83% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.71% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.51% 93.65%

Cross-Links

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PubChem 81886
NPASS NPC47255
LOTUS LTS0192564
wikiData Q83103492