Compounds > serine

serine and prazosin

serine has been researched along with prazosin in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Caron, MG; Cotecchia, S; DeBlasi, A; Leeb-Lundberg, LM; Lefkowitz, RJ1
Agresti, M; Grizzuti, K; Gros, P; Kajiji, S; Safa, AR; Talbot, F; Van Dyke-Phillips, V1
Bordeleau, M; Brooks, KM; Corbett, TJ; de Lannoy, I; Hendrix, JA; Kafka, S; Kamboj, RK; Kapples, KJ; Laws-Ricker, L; Lee, DK; Owolabi, J; Palermo, MG; Rizkalla, G; Shimshock, SJ; Shutske, GM; Tomer, JD; Vargas, HM1
Ahmed, M; Bhuiyan, MA; Hossain, M; Ishiguro, M; Nagaoka, Y; Nagatomo, T; Nakamura, T; Watanabe, M1

Other Studies

4 other study(ies) available for serine and prazosin

ArticleYear
Regulation of adrenergic receptor function by phosphorylation. I. Agonist-promoted desensitization and phosphorylation of alpha 1-adrenergic receptors coupled to inositol phospholipid metabolism in DDT1 MF-2 smooth muscle cells.
    The Journal of biological chemistry, 1987, Mar-05, Volume: 262, Issue:7

    Topics: Animals; Bradykinin; Cell Line; Drug Tolerance; Kinetics; Muscle, Smooth; Norepinephrine; Phosphatidic Acids; Phosphatidylinositols; Phosphorylation; Prazosin; Receptors, Adrenergic, alpha; Serine; Tetradecanoylphorbol Acetate; Threonine

1987
Functional analysis of P-glycoprotein mutants identifies predicted transmembrane domain 11 as a putative drug binding site.
    Biochemistry, 1993, Apr-27, Volume: 32, Issue:16

    Topics: Affinity Labels; Amino Acid Sequence; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Binding Sites; Biological Transport; Cell Membrane; CHO Cells; Cloning, Molecular; Colchicine; Cricetinae; Dactinomycin; Doxorubicin; Drug Resistance; Gramicidin; Iodine Radioisotopes; Kinetics; Membrane Glycoproteins; Mice; Mutagenesis, Site-Directed; Phenylalanine; Prazosin; Serine; Transfection; Vinblastine

1993
Synthesis and structure-activity relationship of the isoindolinyl benzisoxazolpiperidines as potent, selective, and orally active human dopamine D4 receptor antagonists.
    Chembiochem : a European journal of chemical biology, 2002, Oct-04, Volume: 3, Issue:10

    Topics: Administration, Oral; Animals; Apomorphine; Benzyl Compounds; Dizocilpine Maleate; Dopamine D2 Receptor Antagonists; Indoles; Infusions, Parenteral; Isoxazoles; Piperidines; Prazosin; Rats; Receptors, Dopamine D4; Serine; Spiperone; Stereoisomerism; Structure-Activity Relationship; Substrate Specificity

2002
Amino acids of the human alpha1d-adrenergic receptor involved in antagonist binding.
    Journal of pharmacological sciences, 2008, Volume: 106, Issue:1

    Topics: Adrenergic alpha-1 Receptor Antagonists; Adrenergic alpha-Agonists; Adrenergic alpha-Antagonists; Amino Acid Sequence; Aspartic Acid; Binding Sites; Binding, Competitive; Cell Line; Computer Simulation; Glutamic Acid; Humans; Inositol Phosphates; Models, Molecular; Mutagenesis, Site-Directed; Mutation; Phenylephrine; Prazosin; Protein Structure, Tertiary; Radioligand Assay; Receptors, Adrenergic, alpha-1; Serine; Structure-Activity Relationship; Sulfonamides; Tamsulosin; Transfection; Tritium

2008