azides has been researched along with flupenthixol in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (57.14) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, HX; Gesmonde, JF; Hait, WN; Murren, JR; Reiss, M; Yang, JM | 1 |
Ambudkar, SV; Dey, S; Gottesman, MM; Pastan, I; Ramachandra, M | 1 |
Hait, WN; LaVoie, EJ; Makhey, DB; Sullivan, GF; Yang, JM | 1 |
Dey, S; Gottesman, MM; Hafkemeyer, P; Pastan, I | 1 |
Chattopadhyay, A; Dey, S; Ghosh, P; Maki, N; Moitra, K; Silver, C | 1 |
Dey, S; Ghosh, P; Maki, N; Moitra, K | 1 |
Dey, S; Maki, N | 1 |
7 other study(ies) available for azides and flupenthixol
Article | Year |
---|---|
Terfenadine (Seldane): a new drug for restoring sensitivity to multidrug resistant cancer cells.
Topics: Affinity Labels; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Cell Division; Dihydropyridines; Doxorubicin; Drug Resistance; Flupenthixol; Humans; Membrane Glycoproteins; Mice; Rhodamine 123; Rhodamines; Structure-Activity Relationship; Terfenadine; Tumor Cells, Cultured | 1993 |
Evidence for two nonidentical drug-interaction sites in the human P-glycoprotein.
Topics: 3T3 Cells; Affinity Labels; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Binding Sites; Biological Transport; Cell Line; Cyclosporine; Flupenthixol; Humans; Insecta; Iodine Radioisotopes; Mice; Models, Biological; Prazosin; Radioligand Assay; Vanadates; Vinblastine | 1997 |
Inhibitory effect of alkylating modulators on the function of P-glycoprotein.
Topics: ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Breast Neoplasms; Dihydropyridines; Dose-Response Relationship, Drug; Doxorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Flupenthixol; Fluphenazine; Humans; Tumor Cells, Cultured; Vinblastine | 1997 |
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 |
Modulator-induced interference in functional cross talk between the substrate and the ATP sites of human P-glycoprotein.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Allosteric Site; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Binding, Competitive; Catalytic Domain; Cell Line; Dose-Response Relationship, Drug; Flupenthixol; Humans; Hydrolysis; Insecta; Models, Biological; Photoaffinity Labels; Protein Binding; Protein Conformation; Recombinant Proteins; Time Factors; Transfection | 2006 |
Allosteric modulation bypasses the requirement for ATP hydrolysis in regenerating low affinity transition state conformation of human P-glycoprotein.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Allosteric Site; Animals; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Binding Sites; Catalytic Domain; Cell Line; Cell Membrane; Flupenthixol; Humans; Hydrolysis; Insecta; Ligands; Molecular Conformation; Prazosin; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Thioxanthenes; Time Factors; Trypsin; Vanadates | 2006 |
Biochemical and pharmacological properties of an allosteric modulator site of the human P-glycoprotein (ABCB1).
Topics: Allosteric Regulation; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Chromatography, Affinity; Electrophoresis, Polyacrylamide Gel; Flupenthixol; Humans; Phenothiazines; Prazosin; Xanthines | 2006 |