Benzene, (1-methylene-2-propenyl)-

Details

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Internal ID ca3e2f95-50a0-481b-947a-1a9bd49836e0
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name buta-1,3-dien-2-ylbenzene
SMILES (Canonical) C=CC(=C)C1=CC=CC=C1
SMILES (Isomeric) C=CC(=C)C1=CC=CC=C1
InChI InChI=1S/C10H10/c1-3-9(2)10-7-5-4-6-8-10/h3-8H,1-2H2
InChI Key IMJGQTCMUZMLRZ-UHFFFAOYSA-N
Popularity 59 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10
Molecular Weight 130.19 g/mol
Exact Mass 130.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Benzene, (1-methylene-2-propenyl)-
2288-18-8
Phenoprene
2-Phenyl-1,3-butadiene
2-Phenylbutadiene
1,3-Butadiene, 2-phenyl-
(1-Methylene-2-propenyl)benzene
(1-METHYLENEPROP-2-EN-1-YL)BENZENE
(buta-1,3-dien-2-yl)benzene
DTXSID40177422
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzene, (1-methylene-2-propenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9736 97.36%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.4665 46.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9456 94.56%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8957 89.57%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9913 99.13%
CYP3A4 substrate - 0.8139 81.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7136 71.36%
CYP3A4 inhibition - 0.8699 86.99%
CYP2C9 inhibition - 0.9085 90.85%
CYP2C19 inhibition - 0.8150 81.50%
CYP2D6 inhibition - 0.9098 90.98%
CYP1A2 inhibition - 0.6811 68.11%
CYP2C8 inhibition - 0.7737 77.37%
CYP inhibitory promiscuity + 0.5721 57.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6264 62.64%
Carcinogenicity (trinary) Warning 0.5432 54.32%
Eye corrosion + 0.9848 98.48%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8969 89.69%
Skin corrosion - 0.6800 68.00%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7585 75.85%
Micronuclear - 0.9741 97.41%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.9825 98.25%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5464 54.64%
Acute Oral Toxicity (c) III 0.7336 73.36%
Estrogen receptor binding - 0.7164 71.64%
Androgen receptor binding - 0.7820 78.20%
Thyroid receptor binding - 0.7578 75.78%
Glucocorticoid receptor binding - 0.8452 84.52%
Aromatase binding - 0.7362 73.62%
PPAR gamma - 0.6578 65.78%
Honey bee toxicity - 0.9511 95.11%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9855 98.55%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.13% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.42% 94.62%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 86.15% 82.05%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.75% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.54% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.95% 91.11%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 83.93% 81.29%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.78% 93.81%
CHEMBL4267 P37173 TGF-beta receptor type II 83.52% 88.18%

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.
Cinnamomum aromaticum

Cross-Links

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PubChem 137524
NPASS NPC6131