5-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one

Details

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Internal ID 520119ba-a62c-4487-a1bd-4c974b1c5166
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-(1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one
SMILES (Canonical) C1CCN(C1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3
SMILES (Isomeric) C1CCN(C1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3
InChI InChI=1S/C16H19NO3/c18-16(17-9-3-4-10-17)6-2-1-5-13-7-8-14-15(11-13)20-12-19-14/h2,6-8,11H,1,3-5,9-10,12H2
InChI Key XZTCTKKANUDQCW-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19NO3
Molecular Weight 273.33 g/mol
Exact Mass 273.13649347 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-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 + 0.9930 99.30%
Caco-2 + 0.8502 85.02%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6651 66.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9354 93.54%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6664 66.64%
BSEP inhibitior + 0.8667 86.67%
P-glycoprotein inhibitior - 0.5977 59.77%
P-glycoprotein substrate - 0.8703 87.03%
CYP3A4 substrate - 0.5486 54.86%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.5784 57.84%
CYP2C9 inhibition - 0.8585 85.85%
CYP2C19 inhibition - 0.5673 56.73%
CYP2D6 inhibition + 0.7047 70.47%
CYP1A2 inhibition + 0.8566 85.66%
CYP2C8 inhibition - 0.8833 88.33%
CYP inhibitory promiscuity + 0.6654 66.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5407 54.07%
Eye corrosion - 0.9800 98.00%
Eye irritation + 0.5724 57.24%
Skin irritation - 0.6848 68.48%
Skin corrosion - 0.7923 79.23%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7481 74.81%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8072 80.72%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8433 84.33%
Acute Oral Toxicity (c) III 0.7571 75.71%
Estrogen receptor binding + 0.6646 66.46%
Androgen receptor binding + 0.8079 80.79%
Thyroid receptor binding + 0.7280 72.80%
Glucocorticoid receptor binding - 0.6411 64.11%
Aromatase binding + 0.7945 79.45%
PPAR gamma + 0.6051 60.51%
Honey bee toxicity - 0.9267 92.67%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6252 62.52%
Fish aquatic toxicity + 0.7188 71.88%

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 97.03% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.97% 96.77%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 95.81% 83.57%
CHEMBL2581 P07339 Cathepsin D 94.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.59% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.89% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.62% 91.11%
CHEMBL4208 P20618 Proteasome component C5 87.12% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.96% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.90% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.03% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.29% 92.62%
CHEMBL261 P00915 Carbonic anhydrase I 82.86% 96.76%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.32% 96.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.02% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.80% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.90% 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 hispidum
Piper nigrum

Cross-Links

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PubChem 85433734
LOTUS LTS0114512
wikiData Q104201490