Page last updated: 2024-09-03

e 64 and phlorhizin

e 64 has been researched along with phlorhizin in 2 studies

Compound Research Comparison

Studies
(e 64)
Trials
(e 64)
Recent Studies (post-2010)
(e 64)
Studies
(phlorhizin)
Trials
(phlorhizin)
Recent Studies (post-2010) (phlorhizin)
47711031,8598307

Protein Interaction Comparison

ProteinTaxonomye 64 (IC50)phlorhizin (IC50)
Sodium/glucose cotransporter 1Homo sapiens (human)0.2556
Sodium/glucose cotransporter 2Homo sapiens (human)0.1118
Sodium/glucose cotransporter 1 Rattus norvegicus (Norway rat)0.35
Sodium/glucose cotransporter 2Rattus norvegicus (Norway rat)0.096
Solute carrier family 5 member 4Homo sapiens (human)0.016
Prostaglandin D2 receptor 2Homo sapiens (human)0.0607

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Desai, SA; Fay, MP; Furuya, T; Gluzman, IY; Goldberg, DE; Kambhampati, S; Lisk, G; Pain, M; Su, XZ1
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P1

Other Studies

2 other study(ies) available for e 64 and phlorhizin

ArticleYear
Changes in the plasmodial surface anion channel reduce leupeptin uptake and can confer drug resistance in Plasmodium falciparum-infected erythrocytes.
    Antimicrobial agents and chemotherapy, 2008, Volume: 52, Issue:7

    Topics: Animals; Antimalarials; Biological Transport, Active; Cell Membrane Permeability; Cysteine Proteinase Inhibitors; Drug Resistance; Erythrocytes; Genes, Protozoan; Humans; In Vitro Techniques; Ion Channels; Leupeptins; Malaria, Falciparum; Plasmodium falciparum; Protozoan Proteins

2008
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