2003
DOI: 10.1002/chin.200326174
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Synthesis and Antimicrobial Activity of Some Pyrazoline Derivatives of 4(3H)‐Quinazolinones.

Abstract: Fused pyrimidine derivativesFused pyrimidine derivatives R 0515 Synthesis and Antimicrobial Activity of Some Pyrazoline Derivatives of 4(3H)-Quinazolinones. -New compounds incorporating both the quinazolinone and pyrazolinone ring system are synthesized by reaction of hydrazides (IV) with acetoacetate (V). Some of the compounds obtained show good antibacterial and moderate antifungal activity. -(PANDA, J.; SRINIVAS, S. V.; RAO, M. E. B.; PANDA*, C. S.; J. Indian Chem. Soc. 79 (2002) 9, 770-771; Dep. Chem., Ber… Show more

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“…Since the discovery that 3-methylpyrazole and 4-ethylpyrazole have potential medicinal value, there has been a rapid growth in synthesizing new derivatives of pyrazole as anticancer (Manfredini et al 1992;Komeda et al 2000;Gamage et al 2002;MoukhaChafiq et al 2002;Rostom et al 2003;Duivenvoorden et al 2005;Park et al 2005;Keter et al 2009a), antibacterial (Jungheim 1989;Aiello et al 2000;Genin et al 2000a;Kucukguzel et al 2000;El-Gaby et al 2000;Farghaly et al 2001;Moukha-Chafiq et al 2002;Haque et al 2002;Kaymakcıoglu and Rollas 2002;Panda et al 2002;Adnan and Abdel-Aziem 2004;Tanitame et al 2004;Akbas and Berber 2005;Bekhit et al 2005;Bildirici et al 2007;Abunada et al 2008;Radi et al 2010), antiparasitic (Garg et al 1973;Rathelot et al 2002), antiviral (Comber et al 1991;Manfredini et al 1992;Storer et al 1999;Johansson et al 2002;Rostom et al 2003;Sweeney et al 2008), analgesics (Menozzi et al 1997;Pinto et al 1999) antiglycemic agents (Bauer et al 1968;Kees et al 1996;Bebernitz et al 2001) and even as anti-inflammatory agents …”
Section: N N Hmentioning
confidence: 99%
“…Since the discovery that 3-methylpyrazole and 4-ethylpyrazole have potential medicinal value, there has been a rapid growth in synthesizing new derivatives of pyrazole as anticancer (Manfredini et al 1992;Komeda et al 2000;Gamage et al 2002;MoukhaChafiq et al 2002;Rostom et al 2003;Duivenvoorden et al 2005;Park et al 2005;Keter et al 2009a), antibacterial (Jungheim 1989;Aiello et al 2000;Genin et al 2000a;Kucukguzel et al 2000;El-Gaby et al 2000;Farghaly et al 2001;Moukha-Chafiq et al 2002;Haque et al 2002;Kaymakcıoglu and Rollas 2002;Panda et al 2002;Adnan and Abdel-Aziem 2004;Tanitame et al 2004;Akbas and Berber 2005;Bekhit et al 2005;Bildirici et al 2007;Abunada et al 2008;Radi et al 2010), antiparasitic (Garg et al 1973;Rathelot et al 2002), antiviral (Comber et al 1991;Manfredini et al 1992;Storer et al 1999;Johansson et al 2002;Rostom et al 2003;Sweeney et al 2008), analgesics (Menozzi et al 1997;Pinto et al 1999) antiglycemic agents (Bauer et al 1968;Kees et al 1996;Bebernitz et al 2001) and even as anti-inflammatory agents …”
Section: N N Hmentioning
confidence: 99%
“…This gave a great impetus to the search for potential pharmacologically active drugs carrying pyrazole substituents. Pyrazolyl pyrazoline derivatives were found to possess therapeutic activities such as antiinflammatory [3] antimicrobial [4], antiallergic [5], antidiabetic [6] and cardiovascular [7]. The efficiency of the pyrazole derivatives was increased by introducing charged core in its structure either as a cationic (pyrazolium) or anionic center (carboxylate, sulfate …).…”
Section: Introductionmentioning
confidence: 99%