24725-60-8Relevant academic research and scientific papers
Discovery and structure-activity relationship analysis of Staphylococcus aureus sortase A inhibitors
Suree, Nuttee,Yi, Sung Wook,Thieu, William,Marohn, Melanie,Damoiseaux, Robert,Chan, Albert,Jung, Michael E.,Clubb, Robert T.
experimental part, p. 7174 - 7185 (2010/03/30)
Methicillin resistant Staphylococcus aureus (MRSA) is a major health problem that has created a pressing need for new antibiotics. Compounds that inhibit the S. aureus SrtA sortase may function as potent anti-infective agents as this enzyme attaches virulence factors to the cell wall. Using high-throughput screening, we have identified several compounds that inhibit the enzymatic activity of the SrtA. A structure-activity relationship (SAR) analysis led to the identification of several pyridazinone and pyrazolethione analogs that inhibit SrtA with IC50 values in the sub-micromolar range. Many of these molecules also inhibit the sortase enzyme from Bacillus anthracis suggesting that they may be generalized sortase inhibitors.
Efficient N-arylation of pyridazin-3(2H)-ones
Kim, Jeum-Jong,Park, Yong-Dae,Cho, Su-Dong,Kim, Ho-Kyun,Chung, Hyun A.,Lee, Sang-Gyeong,Falck,Yoon, Yong-Jin
, p. 8781 - 8784 (2007/10/03)
A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene. A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene.
