Page last updated: 2024-09-04

clevidipine and quinine

clevidipine has been researched along with quinine in 3 studies

Compound Research Comparison

Studies
(clevidipine)
Trials
(clevidipine)
Recent Studies (post-2010)
(clevidipine)
Studies
(quinine)
Trials
(quinine)
Recent Studies (post-2010) (quinine)
12719626,8593981,099

Protein Interaction Comparison

ProteinTaxonomyclevidipine (IC50)quinine (IC50)
Solute carrier family 22 member 1Mus musculus (house mouse)0.28
Solute carrier family 22 member 2Mus musculus (house mouse)2.8
Potassium channel subfamily K member 2Homo sapiens (human)3.85
ATP-dependent translocase ABCB1Homo sapiens (human)1.7
Cytochrome P450 2D26Rattus norvegicus (Norway rat)0.094
Cytochrome P450 2D6Homo sapiens (human)0.6285
Solute carrier family 22 member 1Rattus norvegicus (Norway rat)2.0333
Cytochrome P450 2D4Rattus norvegicus (Norway rat)1.7

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lombardo, F; Obach, RS; Waters, NJ1
Cantin, LD; Chen, H; Kenna, JG; Noeske, T; Stahl, S; Walker, CL; Warner, DJ1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1

Reviews

1 review(s) available for clevidipine and quinine

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016

Other Studies

2 other study(ies) available for clevidipine and quinine

ArticleYear
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
    Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:7

    Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding

2008
Mitigating the inhibition of human bile salt export pump by drugs: opportunities provided by physicochemical property modulation, in silico modeling, and structural modification.
    Drug metabolism and disposition: the biological fate of chemicals, 2012, Volume: 40, Issue:12

    Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Bile Acids and Salts; Cell Line; Chemical and Drug Induced Liver Injury; Humans; Quantitative Structure-Activity Relationship

2012