937724-67-9Relevant articles and documents
Design, synthesis and biological evaluation of novel fluorinated heterocyclic hybrid molecules based on triazole & quinoxaline scaffolds lead to highly potent antimalarials and antibacterials
Chandra Shekhar, Adimulam,Venkat Lingaiah, Boddupally Pedda,Shanthan Rao, Pamulaparthy,Narsaiah, Banda,Aparna Devi, Allanki,Sijwali, Puran Singh
, p. 393 - 407 (2015/06/22)
A series of novel fluorinated heterocyclic hybrid molecules based on triazole & quinoxaline scaffold were designed, synthesized and evaluated for inhibition of Plasmodium falciparum, a virulent human malaria parasite. Mono and bis triazole tagged quinoxal
Quinoxalinylurea derivatives as a novel class of JSP-1 inhibitors
Zhang, Li,Qiu, Beiying,Xiong, Bing,Li, Xin,Li, Jingya,Wang, Xin,Li, Jia,Shen, Jingkang
, p. 2118 - 2122 (2008/02/01)
A series of quinoxalinylurea-based inhibitors are synthesized and shown to be the novel and potent inhibitors against Jnk Stimulatory Phosphatase-1 (JSP-1), which is a special member of dual-specificity protein phosphatase (DSP) family. Biological assay a