Cargando…
Synthesis and biological evaluation of novel (E)-N'-benzylidene hydrazides as novel c-Met inhibitors through fragment based virtual screening
C-Met plays a crucial role in the development and progression of neoplastic disease. Type II c-Met inhibitors recognise the inactive DFG-out conformation of the kinase, result in better anti-tumour effects due to synergistic effect against the other kinases. According to our previous works, an (E)-N...
Autores principales: | Liang, Jing-wei, Li, Shi-long, Wang, Shan, Li, Wan-qiu, Meng, Fan-hao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968643/ https://www.ncbi.nlm.nih.gov/pubmed/31902266 http://dx.doi.org/10.1080/14756366.2019.1702655 |
Ejemplares similares
-
Benzylidene/2-chlorobenzylidene hydrazides: Synthesis, antimicrobial activity, QSAR studies and antiviral evaluation
por: Kumar, Davinder, et al.
Publicado: (2010) -
(E)-N′-Benzylidene-p-toluenesulfonohydrazide
por: Mehrabi, Hossein, et al.
Publicado: (2008) -
Synthesis Biological Activity of Novel Amino Acid-(N′-Benzoyl) Hydrazide and Amino Acid-(N′-Nicotinoyl) Hydrazide Derivatives
por: Khattab, Sherine N.
Publicado: (2005) -
Virtual fragment screening for novel inhibitors of 6-phosphogluconate dehydrogenase
por: Ruda, Gian Filippo, et al.
Publicado: (2010) -
Design, Synthesis and Biological Evaluation of 4-Benzamidobenzoic Acid Hydrazide Derivatives as Novel Soluble Epoxide Hydrolase Inhibitors
por: Rezaee Zavareh, Elham, et al.
Publicado: (2014)