40205-21-8Relevant articles and documents
Synthesis, inhibition of mycobacterium tuberculosis enoyl-acyl carrier protein reductase and antimycobacterial activity of novel pentacyanoferrate(II)-isonicotinoylhydrazones
Gazzi, Thais P.,Rotta, Mariane,Villela, Anne D.,Rodrigues, Valn's,Martinelli, Leonardo K.B.,Sales, Francisco Adilson M.,Silva De Sousa, Eduardo Henrique,Campos, Maria Martha,Basso, Luiz Augusto,Santos, Diógenes S.,Machado, Pablo
, p. 2028 - 2037 (2017)
Tuberculosis remains among the top causes of death triggered by a single pathogen. Herein, a greener synthetic approach for isonicotinoylhydrazones is described using ultrasound energy. These compounds were used as starting materials for synthesizing pent
Lipophilic analogs of isoniazid with antiproliferative in vitro activity-VIII
Vigorita, Maria Gabriella,Maccari, Rosanna,Ottana, Rosaria,Monforte, Francesca
, p. 306 - 321 (2007/10/03)
Five series of differently-featured Isoniazid (INH) analogs were synthesized and investigated with the aim of extending the specific bioactivity of the parent-drug to AIDS-associated pathologies other than tuberculosis. All compounds were found to be more
Some new 2-aryl-3-isonicotamido-4-thiazolidinones and their 5-carboxymethyl homologues as potential antitubercular and antibacterial agent
Desai,Shukla,Thaker
, p. 239 - 240 (2007/10/02)
-