2-Methylstyrene

Details

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Internal ID 41f6356a-004b-4eb0-9eee-f6bea26cd35d
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 1-ethenyl-2-methylbenzene
SMILES (Canonical) CC1=CC=CC=C1C=C
SMILES (Isomeric) CC1=CC=CC=C1C=C
InChI InChI=1S/C9H10/c1-3-9-7-5-4-6-8(9)2/h3-7H,1H2,2H3
InChI Key NVZWEEGUWXZOKI-UHFFFAOYSA-N
Popularity 457 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10
Molecular Weight 118.18 g/mol
Exact Mass 118.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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611-15-4
2-Vinyltoluene
1-Methyl-2-vinylbenzene
1-Ethenyl-2-methylbenzene
o-Vinyltoluene
O-METHYLSTYRENE
Styrene, o-methyl-
Benzene, 1-ethenyl-2-methyl-
1-ethenyl-2-methyl-benzene
9017-21-4
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-Methylstyrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9782 97.82%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4674 46.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9077 90.77%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9865 98.65%
CYP3A4 substrate - 0.7437 74.37%
CYP2C9 substrate - 0.7067 70.67%
CYP2D6 substrate - 0.7432 74.32%
CYP3A4 inhibition - 0.9169 91.69%
CYP2C9 inhibition - 0.8466 84.66%
CYP2C19 inhibition - 0.7088 70.88%
CYP2D6 inhibition - 0.9350 93.50%
CYP1A2 inhibition + 0.5154 51.54%
CYP2C8 inhibition - 0.9177 91.77%
CYP inhibitory promiscuity - 0.5113 51.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.4777 47.77%
Eye corrosion + 0.9875 98.75%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9252 92.52%
Skin corrosion - 0.7765 77.65%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7643 76.43%
Micronuclear - 0.9541 95.41%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.9830 98.30%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6447 64.47%
Acute Oral Toxicity (c) III 0.8630 86.30%
Estrogen receptor binding - 0.9037 90.37%
Androgen receptor binding - 0.9144 91.44%
Thyroid receptor binding - 0.8491 84.91%
Glucocorticoid receptor binding - 0.9152 91.52%
Aromatase binding - 0.8639 86.39%
PPAR gamma - 0.8971 89.71%
Honey bee toxicity - 0.9506 95.06%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9919 99.19%

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 93.46% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.23% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.61% 94.73%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 85.40% 81.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.65% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.35% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.14% 96.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.67% 93.81%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.07% 96.25%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps

Cross-Links

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PubChem 11904
NPASS NPC241457