cp 65,526 has been researched along with phenylalanine in 2 studies
Studies (cp 65,526) | Trials (cp 65,526) | Recent Studies (post-2010) (cp 65,526) | Studies (phenylalanine) | Trials (phenylalanine) | Recent Studies (post-2010) (phenylalanine) |
---|---|---|---|---|---|
65 | 1 | 5 | 23,695 | 721 | 4,367 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Agresti, M; Grizzuti, K; Gros, P; Kajiji, S; Safa, AR; Talbot, F; Van Dyke-Phillips, V | 1 |
Dey, S; Gottesman, MM; Hafkemeyer, P; Pastan, I | 1 |
2 other study(ies) available for cp 65,526 and phenylalanine
Article | Year |
---|---|
Functional analysis of P-glycoprotein mutants identifies predicted transmembrane domain 11 as a putative drug binding site.
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 |
A single amino acid residue contributes to distinct mechanisms of inhibition of the human multidrug transporter by stereoisomers of the dopamine receptor antagonist flupentixol.
Topics: Adenosine Triphosphate; Alanine; Amino Acid Substitution; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Biological Transport; Dopamine Antagonists; Flupenthixol; HeLa Cells; Humans; Hydrolysis; Iodine Radioisotopes; Mutagenesis, Site-Directed; Phenylalanine; Photoaffinity Labels; Prazosin; Receptors, Dopamine; Stereoisomerism; Substrate Specificity; Tumor Cells, Cultured; Verapamil | 1999 |