102072-85-5Relevant articles and documents
Synthesis and antiproliferative activity of indolizinophthalazine-5,12- dione derivatives, DNA topoisomerase IB inhibitors
Shen, De-Qing,Wu, Zu-Ping,Wu, Xi-Wei,An, Zeng-Yun,Bu, Xiang-Zhang,Gu, Lian-Quan,Huang, Zhi-Shu,An, Lin-Kun
, p. 3938 - 3942 (2010)
A series of novel indolizinophthalazine-5,12-dione derivatives were designed and synthesized by the reaction of 6,7-dichlorophthalazine-5,8-dione with active methylene reagents (AMR) and pyridine derivatives. Some of synthesized compounds exhibited significant in vitro antiproliferative activity at micromolar level toward four human tumor cell lines, including lung adenocarcinoma cell, large-cell lung carcinoma cell, breast carcinoma cell and ardriamycin-resistance breast carcinoma cell. The DNA topoisomerase IB inhibitory assay indicated that DNA topoisomerase IB might be a biological target of the synthesized compounds. A series of novel indolizinophthalazine-5, 12-dione derivatives were synthesized. Their in vitro antiproliferative activity toward four human tumor cell lines and DNA topoisomerase IB inhibitory activity was investigated.
Studies of Phthalazine-5,8-quinone, A Ring Contraction, and Some Novel and Potentially Useful Fluorescent Phthalimides
Parrick, John,Ragunathan, Ramanaranjinie
, p. 211 - 216 (2007/10/02)
Phthalazine-5,8-quinone 3 has been obtained and some derivatives prepared.Treatment of 5,8-dimethoxy 14 and 5-hydroxy-8-methoxy-2,3-dihydrophthalazin-1,4-dione 16 with ceric ammonium nitrate produces an efficient ring contraction reaction to yield the hig
