(E)-7-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylhept-2-en-1-one

Details

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Internal ID 50160c88-7ee0-4154-837b-7cf15c855283
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name (E)-7-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylhept-2-en-1-one
SMILES (Canonical) C1CCN(CC1)C(=O)C=CCCCCC2=CC3=C(C=C2)OCO3
SMILES (Isomeric) C1CCN(CC1)C(=O)/C=C/CCCCC2=CC3=C(C=C2)OCO3
InChI InChI=1S/C19H25NO3/c21-19(20-12-6-3-7-13-20)9-5-2-1-4-8-16-10-11-17-18(14-16)23-15-22-17/h5,9-11,14H,1-4,6-8,12-13,15H2/b9-5+
InChI Key YGEPXHUKZDDRBW-WEVVVXLNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H25NO3
Molecular Weight 315.40 g/mol
Exact Mass 315.18344366 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-7-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylhept-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 + 0.9917 99.17%
Caco-2 + 0.8067 80.67%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7406 74.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9058 90.58%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7697 76.97%
P-glycoprotein inhibitior + 0.6432 64.32%
P-glycoprotein substrate - 0.7920 79.20%
CYP3A4 substrate + 0.5203 52.03%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition + 0.7018 70.18%
CYP2C9 inhibition - 0.8788 87.88%
CYP2C19 inhibition - 0.6068 60.68%
CYP2D6 inhibition + 0.8288 82.88%
CYP1A2 inhibition + 0.8777 87.77%
CYP2C8 inhibition - 0.7521 75.21%
CYP inhibitory promiscuity + 0.8272 82.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5932 59.32%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.4919 49.19%
Skin irritation - 0.7307 73.07%
Skin corrosion - 0.8626 86.26%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4691 46.91%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8192 81.92%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.8782 87.82%
Acute Oral Toxicity (c) III 0.8109 81.09%
Estrogen receptor binding + 0.7227 72.27%
Androgen receptor binding + 0.8779 87.79%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5832 58.32%
Aromatase binding - 0.5333 53.33%
PPAR gamma + 0.5551 55.51%
Honey bee toxicity - 0.9307 93.07%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6252 62.52%
Fish aquatic toxicity + 0.8457 84.57%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.01% 94.45%
CHEMBL2581 P07339 Cathepsin D 97.83% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 97.23% 83.57%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.84% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.90% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.21% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.98% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.59% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.55% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.32% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.10% 96.25%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.45% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.96% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.74% 89.00%
CHEMBL4208 P20618 Proteasome component C5 83.64% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.53% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.93% 95.89%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 80.97% 96.25%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.92% 90.24%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.62% 100.00%

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 puberulum
Piper tuberculatum

Cross-Links

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PubChem 12985527
LOTUS LTS0119942
wikiData Q105348042