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吲唑类支架作为抗菌和抗真菌剂的影响。

Impact of Indazole Scaffold as Antibacterial and Antifungal Agent.

机构信息

Department of Chemistry, Myongji University, Yongin, 17058, South Korea.

Centurion University of Technology and Management, Odisha, India.

出版信息

Curr Top Med Chem. 2022;22(14):1152-1159. doi: 10.2174/1568026622666220512145646.

DOI:10.2174/1568026622666220512145646
PMID:35549876
Abstract

Heterocycles consisting of a nitrogen atom, Indazole, is a pungent, biological, heterocyclic, bicyclic compound possessing electron-rich portions. Indazole is composed of two nitrogen atoms put under the azoles family, further called isoindazolone. It is colorless solid nitrogen- containing heterocyclics with atomic formula-C7H6N2 are extraordinary scaffolds, still identified as isoindazole. Therefore, analogs of Indazole have experienced expert approaches in later times because of its special biological properties, such as anti-microbial, anti-inflammatory, anticancer, anti- HIV and antihypertensive actions. 1H-indazole and 2H-indazole are two toutomeric forms of Indazole. Sometimes, indazole produces three tautomeric forms that are 1H, 2H and 3H tautomers of indazole. 1H-indazole is reliable than 2H-indazole. We should note that a series of derivatives of indazole having 2H toutomers follow hybridization of cyclic systems and act as anti-inflammatory as well as anti-microbial compounds. It formed Indazole itself and derivatives of Indazole in natural products. A sequence of N-methyl-3-aryl inazoles has dominant against bacterial strains like xanthomon as campstris, Baillus cereus, Escherichia coli, Bacillus megaterium and a fungal strain candida albicans found by in-vitro anti-microbial study of indazole derivatives.

摘要

由氮原子组成的杂环化合物,吲唑,是一种刺鼻的、生物活性的、杂环、双环化合物,具有富电子部分。吲唑由两个氮原子组成,属于唑类家族,进一步称为异吲哚酮。它是无色固体含氮杂环化合物,原子式为 C7H6N2,是非常特殊的支架,仍然被鉴定为异吲哚酮。因此,吲唑的类似物因其特殊的生物学性质,如抗微生物、抗炎、抗癌、抗 HIV 和抗高血压作用,在后来受到了专家的关注。1H-吲唑和 2H-吲唑是吲唑的两种互变异构形式。有时,吲唑会产生三种互变异构形式,即吲唑的 1H、2H 和 3H 互变异构体。1H-吲唑比 2H-吲唑更可靠。我们应该注意的是,一系列具有 2H 互变异构体的吲唑衍生物遵循环状系统的杂化,并作为抗炎和抗微生物化合物。它在天然产物中形成吲唑本身和吲唑衍生物。一系列 N-甲基-3-芳基吲唑对黄单胞菌属 campstris、蜡状芽孢杆菌、大肠杆菌、巨大芽孢杆菌和白色念珠菌等细菌菌株具有优势,这是通过吲唑衍生物的体外抗微生物研究发现的。

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