Page last updated: 2024-09-05

troleandomycin and bromocriptine

troleandomycin has been researched along with bromocriptine in 5 studies

Compound Research Comparison

Studies
(troleandomycin)
Trials
(troleandomycin)
Recent Studies (post-2010)
(troleandomycin)
Studies
(bromocriptine)
Trials
(bromocriptine)
Recent Studies (post-2010) (bromocriptine)
56926237,121727499

Protein Interaction Comparison

ProteinTaxonomytroleandomycin (IC50)bromocriptine (IC50)
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)0.532
Beta-1 adrenergic receptorHomo sapiens (human)2.4
Cytochrome P450 3A4Homo sapiens (human)2.4996
Alpha-2A adrenergic receptorHomo sapiens (human)0.015
D(2) dopamine receptorHomo sapiens (human)0.0016
Androgen receptorRattus norvegicus (Norway rat)2.281
Alpha-2B adrenergic receptorHomo sapiens (human)0.035
Alpha-2C adrenergic receptorHomo sapiens (human)0.52
DRattus norvegicus (Norway rat)0.0279
D(3) dopamine receptorRattus norvegicus (Norway rat)0.0279
5-hydroxytryptamine receptor 1ARattus norvegicus (Norway rat)0.0056
Alpha-2B adrenergic receptorRattus norvegicus (Norway rat)0.514
D(1A) dopamine receptorHomo sapiens (human)2.889
Alpha-2C adrenergic receptorRattus norvegicus (Norway rat)0.514
Alpha-2A adrenergic receptorRattus norvegicus (Norway rat)0.514
Alpha-1D adrenergic receptorHomo sapiens (human)0.03
D(1B) dopamine receptorRattus norvegicus (Norway rat)0.0279
5-hydroxytryptamine receptor 2AHomo sapiens (human)0.036
5-hydroxytryptamine receptor 2CHomo sapiens (human)0.532
5-hydroxytryptamine receptor 1BRattus norvegicus (Norway rat)0.0056
D(4) dopamine receptorRattus norvegicus (Norway rat)0.0279
D(3) dopamine receptorHomo sapiens (human)0.0006
5-hydroxytryptamine receptor 2BHomo sapiens (human)0.0083
5-hydroxytryptamine receptor 6Homo sapiens (human)0.022
D(2) dopamine receptorRattus norvegicus (Norway rat)0.0279

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dantzig, AH; Ekins, S; Kim, RB; Lan, LB; Leake, BF; Schuetz, EG; Schuetz, JD; Shepard, RL; Wikel, JH; Winter, MA; Wrighton, SA; Yasuda, K1
Furuya, K; Lan, LB; Sanglard, D; Schuetz, EG; Schuetz, JD; Yasuda, K1
Pratim Roy, P; Roy, K1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Fukui, Y; Matsubayashi, K; Matsumoto, H1

Other Studies

5 other study(ies) available for troleandomycin and bromocriptine

ArticleYear
Three-dimensional quantitative structure-activity relationships of inhibitors of P-glycoprotein.
    Molecular pharmacology, 2002, Volume: 61, Issue:5

    Topics: Animals; Antineoplastic Agents, Phytogenic; ATP Binding Cassette Transporter, Subfamily B, Member 1; Caco-2 Cells; Ergonovine; Fluoxetine; Humans; Models, Molecular; Oxytocics; Protein Conformation; Selective Serotonin Reuptake Inhibitors; Structure-Activity Relationship; Swine; Transfection; Vinblastine

2002
Interaction of cytochrome P450 3A inhibitors with P-glycoprotein.
    The Journal of pharmacology and experimental therapeutics, 2002, Volume: 303, Issue:1

    Topics: Animals; Aryl Hydrocarbon Hydroxylases; ATP Binding Cassette Transporter, Subfamily B, Member 1; Biological Transport; Cell Line; Cells, Cultured; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Dihydroergocryptine; Drug Interactions; Enzyme Inhibitors; Fluconazole; Humans; Mice; Mice, Knockout; Microsomes, Liver; Oxidoreductases, N-Demethylating; Recombinant Proteins; Reserpine; Swine; Tissue Distribution; Transfection; Vinblastine

2002
Comparative chemometric modeling of cytochrome 3A4 inhibitory activity of structurally diverse compounds using stepwise MLR, FA-MLR, PLS, GFA, G/PLS and ANN techniques.
    European journal of medicinal chemistry, 2009, Volume: 44, Issue:7

    Topics: Algorithms; Cytochrome P-450 CYP3A; Cytochrome P-450 CYP3A Inhibitors; Enzyme Inhibitors; Factor Analysis, Statistical; Least-Squares Analysis; Linear Models; Models, Molecular; Neural Networks, Computer; Quantitative Structure-Activity Relationship; Reproducibility of Results

2009
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Contribution of cytochrome P450 3A pathway to bromocriptine metabolism and effects of ferrous iron and hypoxia-re-oxygenation on its elimination in the perfused rat liver.
    The Journal of pharmacy and pharmacology, 1997, Volume: 49, Issue:5

    Topics: Amitrole; Animals; Aryl Hydrocarbon Hydroxylases; Body Fluid Compartments; Bromocriptine; Cell Hypoxia; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Enzyme Inhibitors; Ferrous Compounds; Liver; Male; Oxidation-Reduction; Oxidoreductases, N-Demethylating; Oxygen; Perfusion; Rats; Rats, Wistar; Troleandomycin

1997