Related references
Note: Only part of the references are listed.Design and synthesis of novel 5-aminosalicylate (5-ASA)-4-thiazolinone hybrid derivatives with promising antiproliferative activity
Hajjaj H. M. Abdu-Allah et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2016)
Mycobacterium tuberculosis Folate Metabolism and the Mechanistic Basis for para-Aminosalicylic Acid Susceptibility and Resistance
Yusuke Minato et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2015)
Synthesis and anti-mycobacterial activity of 2-chloronicotinaldehydes based novel 1H-1,2,3-triazolylbenzohydrazides
Pathi Suman et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2015)
Synthesis and evaluation of novel fluorinated pyrazolo-1,2,3-triazole hybrids as antimycobacterial agents
Narender Reddy Emmadi et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2015)
Nitrogen Containing Privileged Structures and their Solid Phase Combinatorial Synthesis
Amit Verma et al.
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING (2013)
Advances in the development of new tuberculosis drugs and treatment regimens
Alimuddin Zumla et al.
NATURE REVIEWS DRUG DISCOVERY (2013)
Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents
Christophe Menendez et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2012)
Identification of Compounds with Anti-Proliferative Activity against Trypanosoma brucei brucei Strain 427 by a Whole Cell Viability Based HTS Campaign
Melissa L. Sykes et al.
PLOS NEGLECTED TROPICAL DISEASES (2012)
Synthesis, antitubercular activity, and SAR study of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides
Alessandro K. Jordao et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2011)
Efficient synthesis and in vitro antitubercular activity of 1,2,3-triazoles as inhibitors of Mycobacterium tuberculosis
Poovan Shanmugavelan et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2011)
New series of isoniazid hydrazones linked with electron-withdrawing substituents
Eva Vavrikova et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2011)
Schiff Bases of Indoline-2,3-dione: Potential Novel Inhibitors of Mycobacterium Tuberculosis (Mtb) DNA Gyrase
Tarek Aboul-Fadl et al.
MOLECULES (2011)
Thiosemicarbazones, semicarbazones, dithiocarbazates and hydrazide/hydrazones: Anti-Mycobacterium tuberculosis activity and cytotoxicity
Fernando R. Pavan et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2010)
Schiff bases of indoline-2,3-dione (isatin) derivatives and nalidixic acid carbohydrazide, synthesis, antitubercular activity and pharmacophoric model building
Tarek Aboul-Fadl et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2010)
Schiff base conjugates of p-aminosalicylic acid as antimycobacterial agents
J Patole et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2006)
Synthesis and anti-inflammatory testing of some new compounds incorporating 5-aminosalicylic acid (5-ASA) as potential prodrugs
AAM Abdel-Alim et al.
ARCHIVES OF PHARMACAL RESEARCH (2005)
The folate pathway is a target for resistance to the drug para-aminosalicylic acid (PAS) in mycobacteria
J Rengarajan et al.
MOLECULAR MICROBIOLOGY (2004)
Cytotoxic activity of some lichen extracts on murine and human cancer cell lines
C Bezivin et al.
PHYTOMEDICINE (2003)
Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling
JC Betts et al.
MOLECULAR MICROBIOLOGY (2002)
Pharmacophore mapping of a series of 2,4-diamino-5-deazapteridine inhibitors of Mycobacterium avium complex dihydrofolate reductase
AK Debnath
JOURNAL OF MEDICINAL CHEMISTRY (2002)
An efficient synthesis of a class of heterobifunctional photo-reactive crosslinkers, labels, and probes
KW Gano et al.
TETRAHEDRON LETTERS (2001)