3-Alkylthio-1,2,4-triazine dimers with potent antimalarial activity
摘要:
We report on the discovery of 3-alkylthio-1,2,4-triazine dimers that are potently toxic to Plasmodium falciparum, with single digit nanomolar activity, and up to several thousand-fold lower toxicity to mammalian cells. They are equipotent against chloroquine-resistant strains of P. falciparum. (c) 2010 Elsevier Ltd. All rights reserved.
One-Pot Synthesis of Some Nitrogen and Sulfur Heterocycles Using Thiosemicarbazide Under Microwave Irradiation in a Solventless System
作者:Majid M. Heravi、Navabeh Nami、Hossien A. Oskooie、Rahim Hekmatshoar
DOI:10.1080/104265090968992
日期:2006.1.1
A thiazolon, triazines, and triazinones were synthesized under microwave irradiation in a solventless system in a very short time and in excellent yields.
在微波辐射下,在无溶剂体系中以极短的时间以极好的收率合成了噻唑酮、三嗪和三嗪酮。
Substituted [(Phenylethanoyl)Amino]Benzamides
申请人:Bruggemeier Ulf
公开号:US20080171786A1
公开(公告)日:2008-07-17
The invention relates to substituted [(phenylethanoyl)amino]benzamides and methods for their preparation, and their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, in particular of inflammatory disorders such as, for example, cutaneous, respiratory tract and cardiovascular disorders such as, for example, arteriosclerosis and coronary heart disease.
The invention relates to substituted [(phenylethanoyl)amino]benzamides and methods for their preparation, and their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, in particular of inflammatory disorders such as, for example, cutaneous, respiratory tract and cardiovascular disorders such as, for example, arteriosclerosis and coronary heart disease.
3-Alkylthio-1,2,4-triazine dimers with potent antimalarial activity
作者:Kung Ban、Sandra Duffy、Yelena Khakham、Vicky M. Avery、Andrew Hughes、Oliver Montagnat、Kasiram Katneni、Eileen Ryan、Jonathan B. Baell
DOI:10.1016/j.bmcl.2010.08.065
日期:2010.10
We report on the discovery of 3-alkylthio-1,2,4-triazine dimers that are potently toxic to Plasmodium falciparum, with single digit nanomolar activity, and up to several thousand-fold lower toxicity to mammalian cells. They are equipotent against chloroquine-resistant strains of P. falciparum. (c) 2010 Elsevier Ltd. All rights reserved.