2-Phenyl-2-butene

Details

Top
Internal ID 5586bd87-d149-4a30-989e-3ffa55235ae5
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropenes
IUPAC Name [(Z)-but-2-en-2-yl]benzene
SMILES (Canonical) CC=C(C)C1=CC=CC=C1
SMILES (Isomeric) C/C=C(/C)\C1=CC=CC=C1
InChI InChI=1S/C10H12/c1-3-9(2)10-7-5-4-6-8-10/h3-8H,1-2H3/b9-3-
InChI Key UGUYQBMBIJFNRM-OQFOIZHKSA-N
Popularity 16 references in papers

Physical and Chemical Properties

Top
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) 3.11
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
cis-2-Phenyl-2-butene
DTXSID40875936
RefChem:1081935
DTXCID101014053
2-PHENYL-2-BUTENE
(Z)-but-2-en-2-ylbenzene
[(Z)-but-2-en-2-yl]benzene
2082-61-3
BENZENE,(1-METHYL-1-PROPENYL)
2-Butene, 2-phenyl-, (Z)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2-Phenyl-2-butene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.9677 96.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5199 51.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8131 81.31%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9824 98.24%
CYP3A4 substrate - 0.8207 82.07%
CYP2C9 substrate - 0.7067 70.67%
CYP2D6 substrate - 0.7432 74.32%
CYP3A4 inhibition - 0.8253 82.53%
CYP2C9 inhibition - 0.8769 87.69%
CYP2C19 inhibition - 0.7952 79.52%
CYP2D6 inhibition - 0.8518 85.18%
CYP1A2 inhibition - 0.7098 70.98%
CYP2C8 inhibition - 0.9203 92.03%
CYP inhibitory promiscuity + 0.5196 51.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5964 59.64%
Carcinogenicity (trinary) Warning 0.5153 51.53%
Eye corrosion + 0.9545 95.45%
Eye irritation + 0.9964 99.64%
Skin irritation + 0.8633 86.33%
Skin corrosion - 0.8630 86.30%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6164 61.64%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.9860 98.60%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5345 53.45%
Acute Oral Toxicity (c) III 0.8515 85.15%
Estrogen receptor binding - 0.9104 91.04%
Androgen receptor binding - 0.8092 80.92%
Thyroid receptor binding - 0.8484 84.84%
Glucocorticoid receptor binding - 0.8704 87.04%
Aromatase binding - 0.8575 85.75%
PPAR gamma - 0.9148 91.48%
Honey bee toxicity - 0.9829 98.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9730 97.30%

Targets

Top

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 88.25% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.17% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.58% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 86.20% 90.17%
CHEMBL2581 P07339 Cathepsin D 85.48% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 80.64% 91.49%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 5358306
NPASS NPC260293