4-Phenyl-2-butenal

Details

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Internal ID 458a5c20-3a63-4441-8383-4e34edaf9551
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (E)-4-phenylbut-2-enal
SMILES (Canonical) C1=CC=C(C=C1)CC=CC=O
SMILES (Isomeric) C1=CC=C(C=C1)C/C=C/C=O
InChI InChI=1S/C10H10O/c11-9-5-4-8-10-6-2-1-3-7-10/h1-7,9H,8H2/b5-4+
InChI Key WLNLUFZWBZXINT-SNAWJCMRSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O
Molecular Weight 146.19 g/mol
Exact Mass 146.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(E)-4-phenylbut-2-enal
2-Butenal, 4-phenyl-
4-PHENYLBUT-2-ENAL
13910-23-1
55177-35-0
4-Phenylcrotonaldehyde
4-phenyl-2-buten-1-al
(2E)-4-phenyl-2-butenal
(E)-4-phenyl-but-2-enal
SCHEMBL145089
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Phenyl-2-butenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9525 95.25%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Plasma membrane 0.4425 44.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9605 96.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7859 78.59%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9657 96.57%
CYP3A4 substrate - 0.7567 75.67%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8109 81.09%
CYP3A4 inhibition - 0.9578 95.78%
CYP2C9 inhibition - 0.9137 91.37%
CYP2C19 inhibition - 0.8049 80.49%
CYP2D6 inhibition - 0.9557 95.57%
CYP1A2 inhibition + 0.5459 54.59%
CYP2C8 inhibition - 0.8937 89.37%
CYP inhibitory promiscuity - 0.5717 57.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6064 60.64%
Carcinogenicity (trinary) Non-required 0.7062 70.62%
Eye corrosion + 0.9953 99.53%
Eye irritation + 0.9918 99.18%
Skin irritation + 0.9658 96.58%
Skin corrosion + 0.9469 94.69%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7763 77.63%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5391 53.91%
skin sensitisation + 0.9930 99.30%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6074 60.74%
Acute Oral Toxicity (c) III 0.8343 83.43%
Estrogen receptor binding - 0.6869 68.69%
Androgen receptor binding - 0.8325 83.25%
Thyroid receptor binding - 0.8844 88.44%
Glucocorticoid receptor binding - 0.6271 62.71%
Aromatase binding + 0.5222 52.22%
PPAR gamma - 0.6992 69.92%
Honey bee toxicity - 0.9374 93.74%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9020 90.20%

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 93.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.41% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.99% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.97% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 83.41% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.55% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.80% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11008054
LOTUS LTS0092728
wikiData Q76416426