2001
DOI: 10.1515/hc.2001.7.2.167
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Synthesis of Some New Unsymmetrical 1,4-Dihydropyridine Derivatives as Potent Antitubercular Agents

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Cited by 12 publications
(13 citation statements)
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“…The 1,4-dihydropyridines recently been shown to possess anti-TB activity. Dihydropyridine derivative 33 was found to be most potent showing 87% inhibition respectively at a concentration of 12.5μg/mL (Gaveriya et al, 2001). While, presence of imidazole group at 4-position and amide group at 3,5-position (34) increased the activity up to 1 μg/mL against Mtb.…”
Section: Quinolonesmentioning
confidence: 96%
“…The 1,4-dihydropyridines recently been shown to possess anti-TB activity. Dihydropyridine derivative 33 was found to be most potent showing 87% inhibition respectively at a concentration of 12.5μg/mL (Gaveriya et al, 2001). While, presence of imidazole group at 4-position and amide group at 3,5-position (34) increased the activity up to 1 μg/mL against Mtb.…”
Section: Quinolonesmentioning
confidence: 96%
“…For background to the pharmaceutical applications of 1,4-dihydropyridine derivatives, see: Gaveriya et al (2001); Shah et al (2000Shah et al ( , 2002; Marchalin et al (2004); Chhillar et al (2006).…”
Section: Related Literaturementioning
confidence: 99%
“…Since the early 1980's the presence of a DHP ring in the structure of 1,4-DHP derivatives has been regarded as a prerequisite for calcium (Ca +2 ) channel modulating properties [3]. So 1,4-DHPs classes of compounds are excellent starting synthons for the development of antitubercular agents [4][5][6]. As a result, newly synthesized generations of 1,4-DHPs possess different pharmacological activities such as anticancer [7], antidiabetic [8], antianginal [9], bronchodilating [10], neurotropic [11], antiallergic [12], anti-inflammatory [13], acaricidal, insecticidal, bactericidal, herbicidal [14] and other pharmacological activities [15].…”
Section: Introductionmentioning
confidence: 99%