3-Butenylbenzene

Details

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Internal ID 42cc8500-3df8-4989-9bb0-57667ad813db
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name but-3-enylbenzene
SMILES (Canonical) C=CCCC1=CC=CC=C1
SMILES (Isomeric) C=CCCC1=CC=CC=C1
InChI InChI=1S/C10H12/c1-2-3-7-10-8-5-4-6-9-10/h2,4-6,8-9H,1,3,7H2
InChI Key PBGVMIDTGGTBFS-UHFFFAOYSA-N
Popularity 190 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) 2.81
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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768-56-9
3-Butenylbenzene
but-3-enylbenzene
Benzene, 3-butenyl-
1-Phenyl-3-butene
1-Butene, 4-phenyl-
4-Phenylbutene-1
4-Phenylbut-1-ene
(but-3-en-1-yl)benzene
but-3-enyl-benzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Butenylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 + 0.9679 96.79%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Plasma membrane 0.4397 43.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9290 92.90%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8717 87.17%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9680 96.80%
CYP3A4 substrate - 0.7399 73.99%
CYP2C9 substrate - 0.8408 84.08%
CYP2D6 substrate + 0.3848 38.48%
CYP3A4 inhibition - 0.9172 91.72%
CYP2C9 inhibition - 0.8891 88.91%
CYP2C19 inhibition - 0.7694 76.94%
CYP2D6 inhibition - 0.9280 92.80%
CYP1A2 inhibition - 0.6008 60.08%
CYP2C8 inhibition - 0.6452 64.52%
CYP inhibitory promiscuity + 0.5248 52.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.5177 51.77%
Eye corrosion + 0.9929 99.29%
Eye irritation + 0.9962 99.62%
Skin irritation + 0.8817 88.17%
Skin corrosion - 0.7916 79.16%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6557 65.57%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.9591 95.91%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6068 60.68%
Acute Oral Toxicity (c) III 0.5288 52.88%
Estrogen receptor binding - 0.7196 71.96%
Androgen receptor binding - 0.7974 79.74%
Thyroid receptor binding - 0.8024 80.24%
Glucocorticoid receptor binding - 0.8011 80.11%
Aromatase binding - 0.7023 70.23%
PPAR gamma - 0.7651 76.51%
Honey bee toxicity - 0.7258 72.58%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9543 95.43%

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
CHEMBL240 Q12809 HERG 98.11% 89.76%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.05% 94.62%
CHEMBL2581 P07339 Cathepsin D 90.27% 98.95%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.07% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.00% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.42% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.74% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.79% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 81.12% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 80.50% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 80.28% 90.17%

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.
Elsholtzia ciliata
Elsholtzia splendens
Mosla chinensis

Cross-Links

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PubChem 13033
NPASS NPC281118