3-(7-Methoxy-1,3-benzodioxol-5-yl)-1-piperidin-1-ylprop-2-en-1-one

Details

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Internal ID 5a87a1c8-6787-4923-bf01-2d9e90a71399
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name 3-(7-methoxy-1,3-benzodioxol-5-yl)-1-piperidin-1-ylprop-2-en-1-one
SMILES (Canonical) COC1=CC(=CC2=C1OCO2)C=CC(=O)N3CCCCC3
SMILES (Isomeric) COC1=CC(=CC2=C1OCO2)C=CC(=O)N3CCCCC3
InChI InChI=1S/C16H19NO4/c1-19-13-9-12(10-14-16(13)21-11-20-14)5-6-15(18)17-7-3-2-4-8-17/h5-6,9-10H,2-4,7-8,11H2,1H3
InChI Key JJAUBODXTTWHQD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H19NO4
Molecular Weight 289.33 g/mol
Exact Mass 289.13140809 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
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-(7-Methoxy-1,3-benzodioxol-5-yl)-1-piperidin-1-ylprop-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 + 0.9893 98.93%
Caco-2 + 0.8797 87.97%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5394 53.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7481 74.81%
P-glycoprotein inhibitior - 0.8684 86.84%
P-glycoprotein substrate - 0.8311 83.11%
CYP3A4 substrate - 0.5431 54.31%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8204 82.04%
CYP3A4 inhibition + 0.7485 74.85%
CYP2C9 inhibition - 0.6993 69.93%
CYP2C19 inhibition + 0.5993 59.93%
CYP2D6 inhibition + 0.5953 59.53%
CYP1A2 inhibition + 0.6624 66.24%
CYP2C8 inhibition - 0.8115 81.15%
CYP inhibitory promiscuity + 0.7268 72.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5381 53.81%
Eye corrosion - 0.9838 98.38%
Eye irritation - 0.6872 68.72%
Skin irritation - 0.7880 78.80%
Skin corrosion - 0.9372 93.72%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7240 72.40%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8280 82.80%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6620 66.20%
Acute Oral Toxicity (c) III 0.7294 72.94%
Estrogen receptor binding + 0.7907 79.07%
Androgen receptor binding + 0.6918 69.18%
Thyroid receptor binding + 0.5999 59.99%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.7501 75.01%
PPAR gamma - 0.7415 74.15%
Honey bee toxicity - 0.8308 83.08%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.7754 77.54%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.47% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.31% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.11% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.97% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.70% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.68% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.59% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.05% 85.14%
CHEMBL2581 P07339 Cathepsin D 88.03% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 87.95% 83.57%
CHEMBL2413 P32246 C-C chemokine receptor type 1 87.94% 89.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.71% 91.11%
CHEMBL4208 P20618 Proteasome component C5 85.34% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.95% 92.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.61% 82.67%
CHEMBL3474 P14555 Phospholipase A2 group IIA 82.41% 94.05%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.39% 90.24%
CHEMBL5028 O14672 ADAM10 81.33% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.74% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.60% 92.94%

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.
Piper nigrum

Cross-Links

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PubChem 72957035
LOTUS LTS0251163
wikiData Q105129500