(2E,4E)-1-Phenyl-2,4-hexadiene

Details

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Internal ID 3dd0687c-c8b9-449f-bbd6-e87f60c6da17
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name [(2E,4E)-hexa-2,4-dienyl]benzene
SMILES (Canonical) CC=CC=CCC1=CC=CC=C1
SMILES (Isomeric) C/C=C/C=C/CC1=CC=CC=C1
InChI InChI=1S/C12H14/c1-2-3-4-6-9-12-10-7-5-8-11-12/h2-8,10-11H,9H2,1H3/b3-2+,6-4+
InChI Key JSQZPUUCMYDLKO-WJPDYIDTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14
Molecular Weight 158.24 g/mol
Exact Mass 158.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.36
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(2Z,4E)-1-Phenyl-2,4-hexadiene

2D Structure

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2D Structure of (2E,4E)-1-Phenyl-2,4-hexadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.9798 97.98%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.3801 38.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8814 88.14%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7251 72.51%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9265 92.65%
CYP3A4 substrate - 0.7422 74.22%
CYP2C9 substrate - 0.8197 81.97%
CYP2D6 substrate - 0.7042 70.42%
CYP3A4 inhibition - 0.9152 91.52%
CYP2C9 inhibition - 0.8517 85.17%
CYP2C19 inhibition - 0.8301 83.01%
CYP2D6 inhibition - 0.9334 93.34%
CYP1A2 inhibition - 0.5556 55.56%
CYP2C8 inhibition - 0.8718 87.18%
CYP inhibitory promiscuity + 0.5051 50.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6064 60.64%
Carcinogenicity (trinary) Warning 0.4850 48.50%
Eye corrosion + 0.9942 99.42%
Eye irritation + 0.9891 98.91%
Skin irritation + 0.9485 94.85%
Skin corrosion + 0.6535 65.35%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5683 56.83%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation + 0.9908 99.08%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6224 62.24%
Acute Oral Toxicity (c) III 0.8296 82.96%
Estrogen receptor binding - 0.5921 59.21%
Androgen receptor binding - 0.8432 84.32%
Thyroid receptor binding - 0.7622 76.22%
Glucocorticoid receptor binding - 0.6847 68.47%
Aromatase binding - 0.5242 52.42%
PPAR gamma - 0.6655 66.55%
Honey bee toxicity - 0.9633 96.33%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 0.9485 94.85%

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
CHEMBL2581 P07339 Cathepsin D 92.87% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.77% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.89% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.34% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.64% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.14% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.96% 95.50%

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.
Artemisia capillaris
Artemisia scoparia

Cross-Links

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PubChem 6429143
NPASS NPC162737