Page last updated: 2024-09-04

abiraterone and flufenamic acid

abiraterone has been researched along with flufenamic acid in 1 studies

Compound Research Comparison

Studies
(abiraterone)
Trials
(abiraterone)
Recent Studies (post-2010)
(abiraterone)
Studies
(flufenamic acid)
Trials
(flufenamic acid)
Recent Studies (post-2010) (flufenamic acid)
942978541,05869202

Protein Interaction Comparison

ProteinTaxonomyabiraterone (IC50)flufenamic acid (IC50)
Aldo-keto reductase family 1 member B10Homo sapiens (human)0.76
TransthyretinHomo sapiens (human)2.9
Prostaglandin G/H synthase 1Homo sapiens (human)2.615
Prostaglandin G/H synthase 2Homo sapiens (human)3.112
Aldo-keto reductase family 1 member C3Homo sapiens (human)1.4901
Aldo-keto reductase family 1 member C2 Homo sapiens (human)1.3467
Aldo-keto reductase family 1 member C1Homo sapiens (human)2.64

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
Bonanni, D; Boschi, D; Carnovale, IM; Cena, C; Costale, A; Giraudo, A; Lolli, ML; Marini, E; Oliaro-Bosso, S; Pippione, AC; Pors, K; Sadiq, M; Zonari, D1

Other Studies

1 other study(ies) available for abiraterone and flufenamic acid

ArticleYear
Hydroxytriazole derivatives as potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors discovered by bioisosteric scaffold hopping approach.
    European journal of medicinal chemistry, 2017, Oct-20, Volume: 139

    Topics: 3-Hydroxysteroid Dehydrogenases; Aldo-Keto Reductase Family 1 Member C3; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Enzyme Inhibitors; Humans; Hydroxyprostaglandin Dehydrogenases; Models, Molecular; Molecular Structure; Structure-Activity Relationship; Triazoles; Tumor Cells, Cultured

2017