3-Cyclohexa-2,4-dien-1-yl-1-phenylprop-2-en-1-one

Details

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Internal ID d42b380b-c0f7-4d62-8693-d1b667c94f11
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 3-cyclohexa-2,4-dien-1-yl-1-phenylprop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-7,9-13H,8H2
InChI Key AGAGXPLQURPGFQ-UHFFFAOYSA-N
Popularity 977 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O
Molecular Weight 210.27 g/mol
Exact Mass 210.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.56
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Cyclohexa-2,4-dien-1-yl-1-phenylprop-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.9050 90.50%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.4567 45.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9550 95.50%
OATP1B3 inhibitior + 0.9621 96.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5492 54.92%
P-glycoprotein inhibitior - 0.9772 97.72%
P-glycoprotein substrate - 0.9386 93.86%
CYP3A4 substrate - 0.5825 58.25%
CYP2C9 substrate - 0.7659 76.59%
CYP2D6 substrate - 0.8265 82.65%
CYP3A4 inhibition - 0.9231 92.31%
CYP2C9 inhibition - 0.7958 79.58%
CYP2C19 inhibition + 0.6700 67.00%
CYP2D6 inhibition - 0.9438 94.38%
CYP1A2 inhibition + 0.8366 83.66%
CYP2C8 inhibition - 0.5814 58.14%
CYP inhibitory promiscuity + 0.7791 77.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6115 61.15%
Eye corrosion + 0.8806 88.06%
Eye irritation + 0.7715 77.15%
Skin irritation + 0.8303 83.03%
Skin corrosion - 0.7882 78.82%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6100 61.00%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5019 50.19%
skin sensitisation + 0.9732 97.32%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6231 62.31%
Acute Oral Toxicity (c) IV 0.4763 47.63%
Estrogen receptor binding + 0.6484 64.84%
Androgen receptor binding - 0.6262 62.62%
Thyroid receptor binding - 0.8261 82.61%
Glucocorticoid receptor binding - 0.8653 86.53%
Aromatase binding + 0.8448 84.48%
PPAR gamma - 0.6699 66.99%
Honey bee toxicity - 0.8839 88.39%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9078 90.78%

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 92.00% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.68% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.79% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.01% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.86% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.51% 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.
Iryanthera polyneura

Cross-Links

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PubChem 20976640
LOTUS LTS0145544
wikiData Q105095063