Page last updated: 2024-09-03

n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine and rosmarinic acid

n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine has been researched along with rosmarinic acid in 1 studies

Compound Research Comparison

Studies
(n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine)
Trials
(n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine)
Recent Studies (post-2010)
(n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine)
Studies
(rosmarinic acid)
Trials
(rosmarinic acid)
Recent Studies (post-2010) (rosmarinic acid)
791161,17415877

Protein Interaction Comparison

ProteinTaxonomyn-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine (IC50)rosmarinic acid (IC50)
Mcl-1Homo sapiens (human)2.0257
bifunctional UDP-N-acetylglucosamine pyrophosphorylase/glucosamine-1-phosphate N-acetyltransferaseMycobacterium tuberculosis H37Rv84.94
Interstitial collagenaseHomo sapiens (human)5.6
Tyrosine-protein kinase FynHomo sapiens (human)2.45
Replicase polyprotein 1abSevere acute respiratory syndrome coronavirus 23.86
Aldo-keto reductase family 1 member B1Homo sapiens (human)3.91
17-beta-hydroxysteroid dehydrogenase type 2Homo sapiens (human)3.72
Alpha-synucleinHomo sapiens (human)0.21
Integrase Human immunodeficiency virus 15.6375

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P1

Other Studies

1 other study(ies) available for n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine and rosmarinic acid

ArticleYear
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
    Bioorganic & medicinal chemistry, 2012, Nov-15, Volume: 20, Issue:22

    Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship

2012