Department of Chemistry, Faculty of Sciences, Ataturk University, 25240 Erzurum, Turkey.
Molecules. 2011 Jun 3;16(6):4660-71. doi: 10.3390/molecules16064660.
The development of resistance to current antifungal therapeutics drives the search for new effective agents. The fact that several acetophenone-derived Mannich bases had shown remarkable antifungal activities in our previous studies led us to design and synthesize some acetophenone-derived Mannich bases, 1-8 and 2-acetylthiophene-derived Mannich base 9, 1-aryl-2-dimethylaminomethyl-2-propen-1-one hydrochloride, to evaluate their antifungal activities. The designed chemical structures have α,β-unsaturated ketone moieties, which are responsible for the bioactivities of the Mannich bases. The aryl part was C₆H₅(1); 4-CH₃C₆H₄ (2); 4-CH₃OC₆H₄ (3); 4-ClC₆H₄ (4); 4-FC₆H₄ (5); 4-BrC₆H₄ (6); 4-HOC₆H₄ (7); 4-NO₂C₆H₄ (8); and C₄H₃S(2-yl) (9). In this study the designed compounds were synthesized by the conventional heating method and also by the microwave irradiation method to compare these methods in terms of reaction times and yields to find an optimum synthetic method, which can be applied for the synthesis of Mannich bases in further studies. Since there are limited number of studies reporting the synthesis of Mannich bases by microwave irradiation, this study may also contribute to the general literature on Mannich bases. Compound 7 was reported for the first time. Antifungal activities of all compounds and synthesis of the compounds by microwave irradiation were also reported for the first time by this study. Fungi (15 species) were used for antifungal activity test. Amphotericin B was tested as an antifungal reference compound. In conclusion, compounds 1-6, and 9, which had more potent (2-16 times) antifungal activity than the reference compound amphotericin B against some fungi, can be model compounds for further studies to develop new antifungal agents. In addition, microwave irradiation can be considered to reduce reaction period, while the conventional method can still be considered to obtain compounds with higher reaction yields in the synthesis of new Mannich bases.
当前抗真菌治疗药物的耐药性发展促使人们寻找新的有效药物。在我们之前的研究中,几种苯乙酮衍生的曼尼希碱表现出了显著的抗真菌活性,这促使我们设计并合成了一些苯乙酮衍生的曼尼希碱,1-8 和 2-乙酰噻吩衍生的曼尼希碱 9、1-芳基-2-二甲基氨甲基-2-丙烯-1-酮盐酸盐,以评估它们的抗真菌活性。设计的化学结构具有α,β-不饱和酮部分,这是曼尼希碱生物活性的原因。芳基部分为 C₆H₅(1);4-CH₃C₆H₄(2);4-CH₃OC₆H₄(3);4-ClC₆H₄(4);4-FC₆H₄(5);4-BrC₆H₄(6);4-HOC₆H₄(7);4-NO₂C₆H₄(8);和 C₄H₃S(2-基)(9)。在这项研究中,设计的化合物通过常规加热法和微波辐射法合成,以比较这两种方法在反应时间和产率方面的差异,从而找到一种最优的合成方法,该方法可进一步应用于曼尼希碱的合成。由于目前报道的微波辐射法合成曼尼希碱的研究数量有限,因此本研究也可能为曼尼希碱的一般文献做出贡献。化合物 7 是首次报道的。本研究还首次报道了所有化合物的抗真菌活性和通过微波辐射合成化合物的情况。该研究使用了 15 种真菌进行抗真菌活性测试。两性霉素 B 被用作抗真菌参考化合物。总之,化合物 1-6 和 9 对一些真菌的抗真菌活性比参考化合物两性霉素 B 更强(2-16 倍),可以作为进一步研究开发新型抗真菌药物的模型化合物。此外,在合成新的曼尼希碱时,微波辐射可以用来缩短反应时间,而常规方法仍然可以用来获得产率更高的化合物。