3-Ethylidenepyrrolidin-2-one

Details

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Internal ID 21a3ef3f-141b-4945-a360-eced91e1c242
Taxonomy Organoheterocyclic compounds > Pyrrolidines > Pyrrolidones > Pyrrolidine-2-ones
IUPAC Name 3-ethylidenepyrrolidin-2-one
SMILES (Canonical) CC=C1CCNC1=O
SMILES (Isomeric) CC=C1CCNC1=O
InChI InChI=1S/C6H9NO/c1-2-5-3-4-7-6(5)8/h2H,3-4H2,1H3,(H,7,8)
InChI Key BUDPEUONKOXMQX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO
Molecular Weight 111.14 g/mol
Exact Mass 111.068413911 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Ethylidenepyrrolidin-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.7917 79.17%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Lysosomes 0.6139 61.39%
OATP2B1 inhibitior - 0.8649 86.49%
OATP1B1 inhibitior + 0.9560 95.60%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9484 94.84%
P-glycoprotein inhibitior - 0.9911 99.11%
P-glycoprotein substrate - 0.9605 96.05%
CYP3A4 substrate - 0.7340 73.40%
CYP2C9 substrate + 0.6159 61.59%
CYP2D6 substrate - 0.9023 90.23%
CYP3A4 inhibition - 0.9880 98.80%
CYP2C9 inhibition - 0.8334 83.34%
CYP2C19 inhibition - 0.8035 80.35%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.6601 66.01%
CYP2C8 inhibition - 0.9958 99.58%
CYP inhibitory promiscuity - 0.8460 84.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5845 58.45%
Eye corrosion - 0.8964 89.64%
Eye irritation + 0.9534 95.34%
Skin irritation - 0.7709 77.09%
Skin corrosion - 0.8959 89.59%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7965 79.65%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.7575 75.75%
skin sensitisation - 0.8596 85.96%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5999 59.99%
Acute Oral Toxicity (c) III 0.6142 61.42%
Estrogen receptor binding - 0.9599 95.99%
Androgen receptor binding - 0.8799 87.99%
Thyroid receptor binding - 0.8881 88.81%
Glucocorticoid receptor binding - 0.9401 94.01%
Aromatase binding - 0.8612 86.12%
PPAR gamma - 0.9254 92.54%
Honey bee toxicity - 0.9364 93.64%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.7955 79.55%

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 89.27% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 84.54% 98.59%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.10% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.03% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.29% 89.34%
CHEMBL2208 P49137 MAP kinase-activated protein kinase 2 81.43% 95.20%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 80.81% 95.72%

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.
Corydalis pallida

Cross-Links

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PubChem 53701396
LOTUS LTS0010220
wikiData Q104946035