1480384-48-2Relevant articles and documents
Design, synthesis, and evaluation of 4-(substituted)phenyl-2-thioxo-3,4- dihydro-1H-chromino[4,3-d]pyrimidin-5-one and 4-(substituted)phenyl-3,4-dihydro- 1H-chromino[4,3-d]pyrimidine-2,5-dione analogs as antitubercular agents
Ambre, Premlata K.,Pissurlenkar, Raghuvir R. S.,Wavhale, Ravindra D.,Shaikh, Mushtaque S.,Khedkar, Vijay M.,Wan, Baojie,Franzblau, Scott G.,Coutinho, Evans C.
, p. 2564 - 2575 (2014)
This paper focuses on the design and antitubercular activity of molecules which are a hybrid of coumarin and pyrimidine nuclei. A set of 16 compounds, viz. 4-(substituted) phenyl-3,4-dihydro-1H-chromino[4,3-d]pyrimidine-2,5-diones and 4-(substituted)phenyl-2-thioxo-3,4-dihydro-1H-chromino[4,3-d]pyrimidin-5- ones have been synthesized using green chemistry principles and evaluated for antitubercular activity by microplate Alamar blue assay (MABA) and lumi-nescence- based low oxygen-recovery assay (LORA) with rifampicin as the standard. The required Mycobacterium tuberculosis H37Rv strain for LORA was cultured using a plasmid bearing an acetamidase promoter driving a bacterial luciferase gene for signal enhancement and were allowed to adapt to low oxygen content in the fermenter. Compounds 5d, 5e, and 5g demonstratedmaximumantitubercular activity,with % inhibition values of 58, 55, and 45 based on MABA and 62, 35 and 37 based on the LORA tests at 128 μM. To understand the relationship between structure and activity, recursive partitioning (RP) models were developed. Two different RP models were built, one based on the antitubercular activity and the other based on the toxicity of the molecules. The decision tree could identify descriptors that discriminate the active and inactive as well as toxic and less toxic 3,4-annelated coumarin analogs. This RP model will be utilized in further work to design more potent molecules. Springer Science+Business Media 2013.
