90958-97-7Relevant articles and documents
Pyrimido[1,2-a]quinoxaline 6-oxide and phenazine 5,10-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi
Lavaggi, Maria Laura,Aguirre, Gabriela,Boiani, Lucia,Orelli, Liliana,Garcia, Beatriz,Cerecetto, Hugo,Gonzalez, Mercedes
, p. 1737 - 1741 (2008/12/20)
Two different families of N-oxide containing heterocycles were evaluated as in vitro growth inhibitors of T. cruzi. Both families of heterocycles were selected from our in-house library of compounds as analogues of active anti-T. cruzi N-oxide containing heterocycles. Derivatives from pyrimido[1,2-a]quinoxaline 6-oxide family were poorly active at the assayed doses. However, phenazine 5,10-dioxide derivatives displayed good to excellent anti-T. cruzi activities. The anti-T. cruzi activity of phenazine derivatives was related to substituent' electronic descriptors, σp-. Derivatives 19, 20 and 23 were the most cytotoxic compounds against the protozoan and became excellent hit for further structural modifications.
Heterocyclic N-Oxides: Part I - Syntheses of 1,2-Dihydroimidazoquinoxaline 5-Oxides & 2,3-Dihydro-1H-pyrimidoquinoxaline 6-Oxides & Their Antiprotozoal Activity
Parthasarathy, P. C.,Joshi, B. S.,Chaphekar, M. R.,Gawad, D. H.,Anandan, Lalitha,et al.
, p. 1250 - 1251 (2007/10/02)
various new substituted 1,2-dihydroimidazoquinoxaline 5-oxides (3,6-16) and 2,3-dihydro-1H-pyrimidoquinoxaline 6-oxides (17-29) have been synthesized.Compounds 11 and 19 display good antiamoebic activity in vivo against Entamoeba histolytica in intestinal and hepatic amoebiasis.