Page last updated: 2024-09-04

alpha-ergocryptine and dihydroergotamine

alpha-ergocryptine has been researched along with dihydroergotamine in 4 studies

Compound Research Comparison

Studies
(alpha-ergocryptine)
Trials
(alpha-ergocryptine)
Recent Studies (post-2010)
(alpha-ergocryptine)
Studies
(dihydroergotamine)
Trials
(dihydroergotamine)
Recent Studies (post-2010) (dihydroergotamine)
74181,450241116

Protein Interaction Comparison

ProteinTaxonomyalpha-ergocryptine (IC50)dihydroergotamine (IC50)
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)0.09
Cytochrome P450 3A4Homo sapiens (human)3.9996
Alpha-2A adrenergic receptorHomo sapiens (human)0.001
D(2) dopamine receptorHomo sapiens (human)0.0089
Alpha-2B adrenergic receptorHomo sapiens (human)0.0039
Alpha-2C adrenergic receptorHomo sapiens (human)0.01
5-hydroxytryptamine receptor 1ARattus norvegicus (Norway rat)0.0007
D(1A) dopamine receptorHomo sapiens (human)2.395
Alpha-1D adrenergic receptorHomo sapiens (human)0.029
5-hydroxytryptamine receptor 2AHomo sapiens (human)0.008
5-hydroxytryptamine receptor 2CHomo sapiens (human)0.09
5-hydroxytryptamine receptor 1BRattus norvegicus (Norway rat)0.0007
D(3) dopamine receptorHomo sapiens (human)0.0053
5-hydroxytryptamine receptor 2BHomo sapiens (human)0.0068
5-hydroxytryptamine receptor 6Homo sapiens (human)0.0032
Multidrug and toxin extrusion protein 1Homo sapiens (human)2.8

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boess, FG; Monsma, FJ; Sleight, AJ1
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
Delaforge, M; Mansuy, D; Peyronneau, MA; Renaud, JP; Riviere, R1

Other Studies

4 other study(ies) available for alpha-ergocryptine and dihydroergotamine

ArticleYear
Identification of residues in transmembrane regions III and VI that contribute to the ligand binding site of the serotonin 5-HT6 receptor.
    Journal of neurochemistry, 1998, Volume: 71, Issue:5

    Topics: Adenylyl Cyclases; Amino Acid Substitution; Binding Sites; Binding, Competitive; Cell Line; Cyclic AMP; Humans; Ligands; Lysergic Acid Diethylamide; Mutagenesis, Site-Directed; Mutation; Receptors, Serotonin; Serotonin; Serotonin Receptor Agonists

1998
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
High affinity of ergopeptides for cytochromes P450 3A. Importance of their peptide moiety for P450 recognition and hydroxylation of bromocriptine.
    European journal of biochemistry, 1994, Aug-01, Volume: 223, Issue:3

    Topics: Animals; Bromocriptine; Cytochrome P-450 CYP2E1; Cytochrome P-450 Enzyme System; Dexamethasone; Dihydroergotamine; Ergolines; Humans; Hydroxylation; Isoenzymes; Lysergic Acid; Microsomes, Liver; Mixed Function Oxygenases; NADP; Oxidation-Reduction; Peptides; Rats; Recombinant Proteins; Saccharomyces cerevisiae; Substrate Specificity

1994