3-Ethylidene-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione

Details

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Internal ID f91d49e6-84f8-4607-a545-234c5307b67e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name 3-ethylidene-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione
SMILES (Canonical) CC=C1C(=O)N2CCCC2C(=O)N1
SMILES (Isomeric) CC=C1C(=O)N2CCCC2C(=O)N1
InChI InChI=1S/C9H12N2O2/c1-2-6-9(13)11-5-3-4-7(11)8(12)10-6/h2,7H,3-5H2,1H3,(H,10,12)
InChI Key ZNFUNIIHSUSXNE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12N2O2
Molecular Weight 180.20 g/mol
Exact Mass 180.089877630 g/mol
Topological Polar Surface Area (TPSA) 49.40 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.01
H-Bond Acceptor 2
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-Ethylidene-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.6817 68.17%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8011 80.11%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5458 54.58%
BSEP inhibitior - 0.9376 93.76%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.7823 78.23%
CYP3A4 substrate - 0.5481 54.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8869 88.69%
CYP3A4 inhibition - 0.8752 87.52%
CYP2C9 inhibition - 0.8732 87.32%
CYP2C19 inhibition - 0.8756 87.56%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.6529 65.29%
CYP2C8 inhibition - 0.9680 96.80%
CYP inhibitory promiscuity - 0.7693 76.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6369 63.69%
Eye corrosion - 0.9755 97.55%
Eye irritation - 0.7603 76.03%
Skin irritation - 0.7530 75.30%
Skin corrosion - 0.9117 91.17%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6611 66.11%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8978 89.78%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.6773 67.73%
Acute Oral Toxicity (c) III 0.5426 54.26%
Estrogen receptor binding - 0.9265 92.65%
Androgen receptor binding - 0.5737 57.37%
Thyroid receptor binding - 0.5511 55.11%
Glucocorticoid receptor binding - 0.7255 72.55%
Aromatase binding - 0.7690 76.90%
PPAR gamma - 0.7419 74.19%
Honey bee toxicity - 0.9386 93.86%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.6266 62.66%

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 95.11% 98.95%
CHEMBL1902 P62942 FK506-binding protein 1A 94.98% 97.05%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.75% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.32% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.17% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.91% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.76% 97.25%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 88.72% 93.03%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.60% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.45% 97.09%
CHEMBL3524 P56524 Histone deacetylase 4 88.08% 92.97%
CHEMBL284 P27487 Dipeptidyl peptidase IV 87.86% 95.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.43% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.01% 91.11%
CHEMBL228 P31645 Serotonin transporter 85.04% 95.51%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.41% 93.04%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.08% 90.24%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.00% 91.03%
CHEMBL3012 Q13946 Phosphodiesterase 7A 83.92% 99.29%
CHEMBL1937 Q92769 Histone deacetylase 2 83.35% 94.75%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.03% 97.64%
CHEMBL217 P14416 Dopamine D2 receptor 82.60% 95.62%
CHEMBL321 P14780 Matrix metalloproteinase 9 81.60% 92.12%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.51% 99.23%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 80.74% 98.99%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.65% 99.18%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.56% 94.78%

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.
Aspidosperma quebracho-blanco

Cross-Links

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PubChem 71435375
LOTUS LTS0036466
wikiData Q105380043