1994
DOI: 10.1016/0223-5234(94)90074-4
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Synthesis of pyridazine acetic acid derivatives possessing aldose reductase inhibitory activity and antioxidant properties

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Cited by 32 publications
(28 citation statements)
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“…Nineteen new [6-(4-methoxyphenyl)-3(2H)-pyridazinone-2-yl]-acetamide (1-10) and 3-[6-(4-methoxyphenyl)-3(2H)-pyridazinone-2-yl]propanamide (11)(12)(13)(14)(15)(16)(17)(18)(19) derivatives have been synthesized in this study. The structures of the compounds have been elucidated by their IR and NMR spectral data and elemental analysis.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Nineteen new [6-(4-methoxyphenyl)-3(2H)-pyridazinone-2-yl]-acetamide (1-10) and 3-[6-(4-methoxyphenyl)-3(2H)-pyridazinone-2-yl]propanamide (11)(12)(13)(14)(15)(16)(17)(18)(19) derivatives have been synthesized in this study. The structures of the compounds have been elucidated by their IR and NMR spectral data and elemental analysis.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, various compounds incorporating a 3(2H)-pyridazinone ring have been synthesized and their pharmacological activities have been reported [10][11][12] . Recently it was reported that a considerable number of 3(2H)-pyridazinone derivatives have analgesic activity [6,[13][14][15][16][17][18] .…”
Section: Introductionmentioning
confidence: 99%
“…Though definitely less potent than epibatidine, which is active in the same test at 1 µg/kg, 1a favourably compared with morphine, active at 2 mg/kg. In addition, 1a exhibited the highest ratio (30) between the maximal non-toxic dose and the minimal analgesic dose, when compared to morphine (10) and epibatidine (7). It should be noted that reversion of the chloropyridazine substituent from N 3 to N 8 as in 2a, or the insertion on N 8 of an alkyl (1c) or a propionyl group (1b), markedly reduced or -as for 1b -abolished the activity.…”
mentioning
confidence: 93%
“…For this purpose, various compounds incorporating a pyridazinone ring have been synthesized and their pharmacological activities have been reported 1,2 . It has been reported that a considerable number of 3(2H)-pyridazinone derivatives bear analgesic activity.…”
Section: Introductionmentioning
confidence: 99%