首页> 外文期刊>Advances in BioResearch >SYNTHESIS OF SOME NOVEL 2-(4- SUBSTITUTED)-1-H-INDOLE-3-CARBALDEHYDE DERIVATIVE AS POTENT ANTI-INFLAMMATORY AGENTS
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SYNTHESIS OF SOME NOVEL 2-(4- SUBSTITUTED)-1-H-INDOLE-3-CARBALDEHYDE DERIVATIVE AS POTENT ANTI-INFLAMMATORY AGENTS

机译:一些新的2-(4-取代的)-1-H-Indole-3-氨基醛衍生物的合成为有效的抗炎剂

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We have made an attempt in the current study to synthesize eight novel indole derivatives (5a-h) and evaluate them for anti-inflammatory activity using Carrageenan-induced rat paw edema method.In the first step, we synthesized substituted acetophenone phenyl hydrozone(3a-h) by using phenyl hydrazine and substituted acetophenone in the presence of acetic acid and H2O.The substituted acetophenone phenyl hydrozone(3a-h) was further reacted with Vilsmeier-Hack reagent (POCl3–DMF) at 0-50C to afforded 2-(4- substituted)-1-H-indole-3-carbaldehyde (5a-h).The final indole derivatives (5a-h) were synthesized and recrystallized using ethanol.The structure of the final compound has been confirmed on the basis of FTIR and 1H NMR.All the values of FT-IR, 1H NMR, melting point, solubility and TLC were found to be prominent.The pharmacological screening by Carrageenan-induced rat paws edema method for antiinflammatiory activity revels that synthesized compounds 5a and 5f were found to be the most potent with compare to standard drugs Diclofenac sodium.
机译:我们试图在目前的研究中合成八种新型吲哚衍生物(5A-H),并使用角叉菜胶诱导的大鼠爪子水肿方法评价它们进行抗炎活动。第一步,我们合成取代的苯乙酮苯基氢羟基(3A -H)通过在乙酸和H 2 O存在下使用苯基肼并取代苯乙酮。在0-50℃下进一步与Vilsmeier-Hack试剂(POCL3-DMF)进一步反应取代的苯乙酮苯基氢苯基(3A-H),得到2- (4-取代的)-1-H-吲哚-3-丙醛(5A-H)。使用乙醇合成并重结晶最终吲哚衍生物(5A-H)。基于的基础上证实了最终化合物的结构FTIR和1H NMR.ALLEALLESS的FT-IR,1H NMR,熔点,溶解度和TLC的值突出。通过角叉菜胶诱导的大鼠爪子的药理学筛查用于抗炎化合物5a和5f的抗炎化合物活性陶醉方法的水肿方法发现是最多的锅与标准药物双氯芬酸钠进行比较。

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