7-(1,3-Benzodioxol-5-yl)-1-piperidin-1-ylhept-6-en-1-one

Details

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Internal ID 86ee44b7-adb4-41fa-83c9-ed7af37d88fb
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 7-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylhept-6-en-1-one
SMILES (Canonical) C1CCN(CC1)C(=O)CCCCC=CC2=CC3=C(C=C2)OCO3
SMILES (Isomeric) C1CCN(CC1)C(=O)CCCCC=CC2=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/h4,8,10-11,14H,1-3,5-7,9,12-13,15H2
InChI Key MIWPBXQTBYPJEF-UHFFFAOYSA-N
Popularity 2 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 3.80
Atomic LogP (AlogP) 4.00
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 7-(1,3-Benzodioxol-5-yl)-1-piperidin-1-ylhept-6-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 + 0.9933 99.33%
Caco-2 + 0.7846 78.46%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7436 74.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9066 90.66%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9265 92.65%
P-glycoprotein inhibitior + 0.7031 70.31%
P-glycoprotein substrate - 0.8580 85.80%
CYP3A4 substrate - 0.5426 54.26%
CYP2C9 substrate + 0.6133 61.33%
CYP2D6 substrate - 0.8159 81.59%
CYP3A4 inhibition + 0.7662 76.62%
CYP2C9 inhibition - 0.8726 87.26%
CYP2C19 inhibition + 0.5434 54.34%
CYP2D6 inhibition + 0.7155 71.55%
CYP1A2 inhibition + 0.8700 87.00%
CYP2C8 inhibition - 0.8655 86.55%
CYP inhibitory promiscuity + 0.8031 80.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5711 57.11%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.6326 63.26%
Skin irritation - 0.7585 75.85%
Skin corrosion - 0.8563 85.63%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7444 74.44%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8245 82.45%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8801 88.01%
Acute Oral Toxicity (c) III 0.8088 80.88%
Estrogen receptor binding + 0.7265 72.65%
Androgen receptor binding + 0.8874 88.74%
Thyroid receptor binding + 0.6138 61.38%
Glucocorticoid receptor binding - 0.6645 66.45%
Aromatase binding + 0.6011 60.11%
PPAR gamma + 0.5775 57.75%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5652 56.52%
Fish aquatic toxicity + 0.7449 74.49%

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 96.07% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.57% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.32% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.02% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.11% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.62% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.82% 96.77%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 91.71% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.68% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.78% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.01% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.49% 90.00%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 84.53% 96.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.14% 86.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.50% 93.99%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 81.04% 90.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.42% 94.80%
CHEMBL5028 O14672 ADAM10 80.38% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.13% 95.89%

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 85413392
LOTUS LTS0149354
wikiData Q105165263