Cargando…
Phenoxyacetohydrazide Schiff Bases: β-Glucuronidase Inhibitors
Phenoxyacetohydrazide Schiff base analogs 1–28 have been synthesized and their in vitro β-glucouoronidase inhibition potential studied. Compounds 1 (IC(50) = 9.20 ± 0.32 µM), 5 (IC(50) = 9.47 ± 0.16 µM), 7 (IC(50) = 14.7 ± 0.19 µM), 8 (IC(50) = 15.4 ± 1.56 µM), 11 (IC(50) = 19.6 ± 0.62 µM), 12 (IC(5...
Autores principales: | Jamil, Waqas, Perveen, Shagufta, Shah, Syed Adnan Ali, Taha, Muhammad, Ismail, Nor Hadiani, Perveen, Shahnaz, Ambreen, Nida, Khan, Khalid M., Choudhary, Muhammad I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271590/ https://www.ncbi.nlm.nih.gov/pubmed/24968334 http://dx.doi.org/10.3390/molecules19078788 |
Ejemplares similares
-
Synthesis, Crystal Structure, DFT Studies and Evaluation of the Antioxidant Activity of 3,4-Dimethoxybenzenamine Schiff Bases
por: Aziz, Ahmad Nazif, et al.
Publicado: (2014) -
Synthesis of 2-Aminopyrimidine Derivatives and Their Evaluation as β-Glucuronidase Inhibitors: In Vitro and In Silico Studies
por: Iqbal, Sarosh, et al.
Publicado: (2022) -
2-Phenoxyacetohydrazide
por: Fun, Hoong-Kun, et al.
Publicado: (2009) -
Synthesis of Novel Bisindolylmethane Schiff bases and Their Antibacterial Activity
por: Imran, Syahrul, et al.
Publicado: (2014) -
Synthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent β-Glucuronidase Inhibitors
por: Taha, Muhammad, et al.
Publicado: (2019)