5-(6-Methoxy-1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one

Details

Top
Internal ID b65c7e15-d067-4412-83ca-98f6fd7f8c00
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-(6-methoxy-1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one
SMILES (Canonical) COC1=CC2=C(C=C1CCC=CC(=O)N3CCCC3)OCO2
SMILES (Isomeric) COC1=CC2=C(C=C1CCC=CC(=O)N3CCCC3)OCO2
InChI InChI=1S/C17H21NO4/c1-20-14-11-16-15(21-12-22-16)10-13(14)6-2-3-7-17(19)18-8-4-5-9-18/h3,7,10-11H,2,4-6,8-9,12H2,1H3
InChI Key SXMGPVCNUOXFBE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H21NO4
Molecular Weight 303.35 g/mol
Exact Mass 303.14705815 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-(6-Methoxy-1,3-benzodioxol-5-yl)-1-pyrrolidin-1-ylpent-2-en-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9786 97.86%
Caco-2 + 0.8235 82.35%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5232 52.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9064 90.64%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5848 58.48%
BSEP inhibitior + 0.9339 93.39%
P-glycoprotein inhibitior - 0.5717 57.17%
P-glycoprotein substrate - 0.7587 75.87%
CYP3A4 substrate + 0.5092 50.92%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.8425 84.25%
CYP3A4 inhibition + 0.7600 76.00%
CYP2C9 inhibition - 0.6052 60.52%
CYP2C19 inhibition + 0.6240 62.40%
CYP2D6 inhibition - 0.5524 55.24%
CYP1A2 inhibition + 0.5496 54.96%
CYP2C8 inhibition - 0.8388 83.88%
CYP inhibitory promiscuity + 0.6655 66.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9240 92.40%
Carcinogenicity (trinary) Non-required 0.5019 50.19%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.8837 88.37%
Skin irritation - 0.7784 77.84%
Skin corrosion - 0.9102 91.02%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6637 66.37%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6340 63.40%
skin sensitisation - 0.8322 83.22%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6914 69.14%
Acute Oral Toxicity (c) III 0.6718 67.18%
Estrogen receptor binding + 0.6676 66.76%
Androgen receptor binding - 0.5516 55.16%
Thyroid receptor binding + 0.7600 76.00%
Glucocorticoid receptor binding + 0.6559 65.59%
Aromatase binding + 0.6962 69.62%
PPAR gamma - 0.5783 57.83%
Honey bee toxicity - 0.8891 88.91%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5655 56.55%
Fish aquatic toxicity + 0.7395 73.95%

Targets

Top

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 96.68% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.67% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.14% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.30% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.31% 98.95%
CHEMBL4208 P20618 Proteasome component C5 90.32% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.69% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.56% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.24% 91.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.83% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.40% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.08% 99.17%
CHEMBL2413 P32246 C-C chemokine receptor type 1 86.25% 89.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.37% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.66% 90.71%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 81.16% 90.95%
CHEMBL5028 O14672 ADAM10 81.03% 97.50%

Plants that contains it

Top
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 reticulatum

Cross-Links

Top
PubChem 73817305
LOTUS LTS0250660
wikiData Q105263193