Pharmacological Evaluation of Novel Hydrazide and Hydrazone Derivatives: Anti-Inflammatory and Analgesic Potential in Preclinical Models
Hydrazones, characterized by their C=N–NH functional group, are promising candidates in medicinal chemistry due to their ability to interact with biological targets. This study evaluated the anti-inflammatory and analgesic properties of <i>N</i>-pyrrolylcarbohydrazide (<b>1</b&g...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-03-01
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| Series: | Molecules |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1420-3049/30/7/1472 |
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| Summary: | Hydrazones, characterized by their C=N–NH functional group, are promising candidates in medicinal chemistry due to their ability to interact with biological targets. This study evaluated the anti-inflammatory and analgesic properties of <i>N</i>-pyrrolylcarbohydrazide (<b>1</b>) and four pyrrole hydrazone derivatives (<b>1A–D</b>) in male Wistar rats (6 weeks old). Anti-inflammatory activity was assessed using a carrageenan-induced paw edema model, while formalin, tail flick, and paw withdrawal tests evaluated analgesia. Compound <b>1</b> exhibited dose-dependent anti-inflammatory activity. At 20 mg/kg, significant edema reductions were observed at the 2nd (<i>p</i> = 0.035) and 3rd hours (<i>p</i> = 0.022), while at 40 mg/kg, reductions remained significant at the 2nd (<i>p</i> = 0.008) and 3rd hours (<i>p</i> = 0.046). Compound <b>1A</b> showed pronounced effects at 20 mg/kg at the 2nd (<i>p</i> = 0.005), 3rd (<i>p</i> < 0.001), and 4th hours (<i>p</i> = 0.004). Other compounds demonstrated minimal or no activity. Analgesic evaluation revealed that at 40 mg/kg, compound <b>1</b> significantly reduced paw-licking time in the second phase (<i>p</i> = 0.038). Compounds <b>1B</b>, <b>1C</b>, and <b>1D</b> exhibited transient effects in the first phase only (<i>p</i> < 0.05). Compound <b>1A</b> lacked significant analgesic activity. The findings suggest that structural modifications may enhance efficacy for broader therapeutic applications. |
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| ISSN: | 1420-3049 |