phenylalanine and wb 4101

phenylalanine has been researched along with wb 4101 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Daly, CJ; Heeley, RP; MacKenzie, JF; McGrath, JC; Pediani, JD	1
Gaivin, RJ; Gonzalez-Cabrera, P; Perez, DM; Ross, SA; Waugh, DJ; Yun, J; Zuscik, MJ	1

Other Studies

2 other study(ies) available for phenylalanine and wb 4101

Article	Year
Single-cell recombinant pharmacology: bovine alpha(1a)-adrenoceptors in rat-1 fibroblasts release intracellular ca(2+), display subtype-characteristic agonism and antagonism, and exhibit an antagonist-reversible inverse concentration-response phase. The Journal of pharmacology and experimental therapeutics, 2000, Volume: 293, Issue:3 Topics: Adrenergic alpha-1 Receptor Agonists; Adrenergic alpha-1 Receptor Antagonists; Animals; Calcium Signaling; Cattle; Dioxanes; Dose-Response Relationship, Drug; Imidazoles; Phenylalanine; Piperazines; Prazosin; Rats; Receptors, Adrenergic, alpha-1; Recombinant Proteins; Reverse Transcriptase Polymerase Chain Reaction; Tetrahydronaphthalenes	2000
Phe-308 and Phe-312 in transmembrane domain 7 are major sites of alpha 1-adrenergic receptor antagonist binding. Imidazoline agonists bind like antagonists. The Journal of biological chemistry, 2001, Jul-06, Volume: 276, Issue:27 Topics: Adrenergic alpha-1 Receptor Antagonists; Adrenergic alpha-Antagonists; Amino Acid Sequence; Animals; Cell Membrane; Clonidine; Conserved Sequence; Cricetinae; Dihydropyridines; Dioxanes; Humans; Imidazoles; Models, Molecular; Molecular Sequence Data; Oxymetazoline; Phenylalanine; Piperazines; Prazosin; Protein Structure, Secondary; Rats; Receptors, Adrenergic, alpha-1; Structure-Activity Relationship	2001

Article

Year

Single-cell recombinant pharmacology: bovine alpha(1a)-adrenoceptors in rat-1 fibroblasts release intracellular ca(2+), display subtype-characteristic agonism and antagonism, and exhibit an antagonist-reversible inverse concentration-response phase.

The Journal of pharmacology and experimental therapeutics, 2000, Volume: 293, Issue:3

Topics: Adrenergic alpha-1 Receptor Agonists; Adrenergic alpha-1 Receptor Antagonists; Animals; Calcium Signaling; Cattle; Dioxanes; Dose-Response Relationship, Drug; Imidazoles; Phenylalanine; Piperazines; Prazosin; Rats; Receptors, Adrenergic, alpha-1; Recombinant Proteins; Reverse Transcriptase Polymerase Chain Reaction; Tetrahydronaphthalenes

2000

Phe-308 and Phe-312 in transmembrane domain 7 are major sites of alpha 1-adrenergic receptor antagonist binding. Imidazoline agonists bind like antagonists.

The Journal of biological chemistry, 2001, Jul-06, Volume: 276, Issue:27

Topics: Adrenergic alpha-1 Receptor Antagonists; Adrenergic alpha-Antagonists; Amino Acid Sequence; Animals; Cell Membrane; Clonidine; Conserved Sequence; Cricetinae; Dihydropyridines; Dioxanes; Humans; Imidazoles; Models, Molecular; Molecular Sequence Data; Oxymetazoline; Phenylalanine; Piperazines; Prazosin; Protein Structure, Secondary; Rats; Receptors, Adrenergic, alpha-1; Structure-Activity Relationship

2001