2010
DOI: 10.1016/j.ejmech.2010.07.032
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Synthesis and pharmacological study of 1-acetyl/propyl-3-aryl-5-(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)-2-pyrazoline

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Cited by 76 publications
(52 citation statements)
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“…Balakrishna Kalluraya et al 39 synthesized a series of acetyl/propyl pyrazolines carrying 5-aryloxypyrazole moiety (2l) and investigated them for their anti-inflammatory and analgesic activity showing that presence of aryloxy group in the 5th position will decreased the anti-inflammatory and analgesic activity when compared with that of 5-chloro derivatives.…”
Section: P Vaidya Et Almentioning
confidence: 99%
See 1 more Smart Citation
“…Balakrishna Kalluraya et al 39 synthesized a series of acetyl/propyl pyrazolines carrying 5-aryloxypyrazole moiety (2l) and investigated them for their anti-inflammatory and analgesic activity showing that presence of aryloxy group in the 5th position will decreased the anti-inflammatory and analgesic activity when compared with that of 5-chloro derivatives.…”
Section: P Vaidya Et Almentioning
confidence: 99%
“…Girisha et al 46 prepared a series of acetyl/propyl pyrazolines (2s) carrying a pyrazole moiety reporting that compounds bearing electron withdrawing nitro group in the arylmoiety showed the highest analgesic activity. P.K.…”
Section: P Vaidya Et Almentioning
confidence: 99%
“…In a subsequent study, we continued with our work towards the modification of N-carboxymethyl rhodanines by introducing different groups at the 5-position of these compounds to give four different series of analogues, including 19a-x, 20a-t, 21a-p and 22a-x ( Figure 11) [50][51][52][53] Molecules containing a pyrazole ring are known to possess a wide variety of biological activities [54,55], and there has been a recent increase in studies directed towards the use of pyrazole derivatives as potential antimicrobial agents [56][57][58][59][60]. With this in mind, we designed and synthesized a new series of pyrazole-based N-carboxymethyl rhodanines (23a-p) and evaluated their antimicrobial activity ( Figure 12) [61].…”
Section: Naohmentioning
confidence: 99%
“…Recently pyrazole and thiazole based pyrazolines have emerged as an attractive lead compounds in drug development due to their antimicrobial activity profile [31][32][33][34] .…”
Section: Oriental Journal Of Chemistrymentioning
confidence: 99%