p-Propenyltoluene

Details

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Internal ID 1880e818-3e6d-428c-bce5-f929acd233a5
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 1-methyl-4-prop-1-enylbenzene
SMILES (Canonical) CC=CC1=CC=C(C=C1)C
SMILES (Isomeric) CC=CC1=CC=C(C=C1)C
InChI InChI=1S/C10H12/c1-3-4-10-7-5-9(2)6-8-10/h3-8H,1-2H3
InChI Key LSMSSYSRCUNIFX-UHFFFAOYSA-N
Popularity 9 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 3.30
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-methyl-4-propenyl-benzene
2698-14-8
DTXSID701345961
1-Methyl-4-(1-propen-1-yl)benzene

2D Structure

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2D Structure of p-Propenyltoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9530 95.30%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.5042 50.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9412 94.12%
OATP1B3 inhibitior + 0.9688 96.88%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7506 75.06%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.7721 77.21%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7486 74.86%
CYP3A4 inhibition - 0.9196 91.96%
CYP2C9 inhibition - 0.9065 90.65%
CYP2C19 inhibition - 0.8897 88.97%
CYP2D6 inhibition - 0.9244 92.44%
CYP1A2 inhibition - 0.7034 70.34%
CYP2C8 inhibition - 0.9425 94.25%
CYP inhibitory promiscuity - 0.6931 69.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5464 54.64%
Carcinogenicity (trinary) Warning 0.4783 47.83%
Eye corrosion + 0.9935 99.35%
Eye irritation + 0.9974 99.74%
Skin irritation + 0.9253 92.53%
Skin corrosion - 0.8761 87.61%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5768 57.68%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7307 73.07%
skin sensitisation + 0.9870 98.70%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5464 54.64%
Acute Oral Toxicity (c) III 0.8438 84.38%
Estrogen receptor binding - 0.8515 85.15%
Androgen receptor binding - 0.6993 69.93%
Thyroid receptor binding - 0.8645 86.45%
Glucocorticoid receptor binding - 0.8820 88.20%
Aromatase binding - 0.8438 84.38%
PPAR gamma - 0.8894 88.94%
Honey bee toxicity - 0.9487 94.87%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.9300 93.00%
Fish aquatic toxicity + 0.9574 95.74%

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 96.49% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.54% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.74% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 87.45% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 83.81% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.96% 94.62%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.97% 90.24%

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.
Glycyrrhiza glabra

Cross-Links

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PubChem 523730
LOTUS LTS0010002
wikiData Q105156639