Category: ruthenium-catalysts. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 2-Chloro-6-nitrobenzo[d]thiazole, is researched, Molecular C7H3ClN2O2S, CAS is 2407-11-6, about Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives. Author is Delmas, Florence; Avellaneda, Antonio; Di Giorgio, Carole; Robin, Maxime; De Clercq, Erik; Timon-David, Pierre; Galy, Jean-Pierre.
(1,3-Benzothiazol-2-yl) amino-9-(10H)-acridinones were synthesized via a procedure based on the Ullman reaction and were assessed for their in vitro antileishmanial and anti-HIV activities. Two derivatives, 4-(6-nitro-benzothiazol-2-ylamino)-10H-acridin-9-one (I) and 1-(6-amino-benzothiazol-2-ylamino)-10H-acridin-9-one (II), revealed a selective antileishmanial activity, mainly due to amastigote-specific toxicity. Results suggested that the addition of a benzothiazole group on a parent amino-9-(10H)-acridinone ring could enhance antileishmanial abilities, the presence of a 6-amino-benzothiazole group on position 2 amino chain or a 6-nitro-benzothiazole group on position 4 amino chain was essential for specific anti-amastigote properties.
In some applications, this compound(2407-11-6)Category: ruthenium-catalysts is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI