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1.
Designed P-glycoprotein inhibitors with triazol-tetrahydroisoquinoline-core increase doxorubicin-induced mortality in multidrug resistant K562/A02 cells.
Bioorg Med Chem
; 27(15): 3347-3357, 2019 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31202598
2.
Design, synthesis and biological evaluation of N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-4-oxo-3,4-dihydrophthalazine-1-carboxamide derivatives as novel P-glycoprotein inhibitors reversing multidrug resistance.
Bioorg Chem
; 86: 166-175, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30710850
3.
Discovery to solve multidrug resistance: Design, synthesis, and biological evaluation of novel agents.
Arch Pharm (Weinheim)
; 352(10): e1900127, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31441108
4.
Synthesis and biological evaluation of JL-A7 derivatives as potent ABCB1 inhibitors.
Bioorg Med Chem
; 25(15): 4194-4202, 2017 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28645831
5.
Design, synthesis and evaluation of a novel series of inhibitors reversing P-glycoprotein-mediated multidrug resistance.
Chem Biol Drug Des
; 92(3): 1708-1716, 2018 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29786944
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