Abstract:
:A series of pyrazine-2-carboxylic acid hydrazide derivatives were synthesized and screened for their activity against Mycobacterium tuberculosis. The results show that pyrazine-2-carboxylic acid hydrazide-hydrazone derivatives 3a-l were less active than pyrazinamide. In contrast, the N(4)-ethyl-N(1)-pyrazinoyl-thiosemicarbazide 4 showed the highest activity against M. tuberculosis H(37)Rv (IC(90) = 16.87 microg/mL). Details of the structure-activity and structure-cytotoxicity relationships are discussed.
journal_name
Eur J Med Chemjournal_title
European journal of medicinal chemistryauthors
Abdel-Aziz M,Abdel-Rahman HMdoi
10.1016/j.ejmech.2010.04.025subject
Has Abstractpub_date
2010-08-01 00:00:00pages
3384-8issue
8eissn
0223-5234issn
1768-3254pii
S0223-5234(10)00307-7journal_volume
45pub_type
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