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具有抗菌活性的杂环喹啉-磺胺类配合物(M)衍生物。

Hybrid Quinoline-Sulfonamide Complexes (M) Derivatives with Antimicrobial Activity.

机构信息

Faculty of Chemistry, Alexandru Ioan Cuza University of Iasi, 11 Carol Bvd, 700506 Iasi, Romania.

Institute of Interdisciplinary Research-CERNESIM Center, Alexandru Ioan Cuza University of Iasi, 11 Carol Bvd, 700506 Iasi, Romania.

出版信息

Molecules. 2020 Jun 26;25(12):2946. doi: 10.3390/molecules25122946.

DOI:10.3390/molecules25122946
PMID:32604828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7356327/
Abstract

Two new series of hybrid quinoline-sulfonamide complexes (M: Zn, Cu, Co and Cd) derivatives () were designed, synthesized and tested for their antimicrobial activity. The synthesis is straightforward and efficient, involving two steps: acylation of aminoquinoline followed by complexation with metal acetate (Cu, Co and Cd) or chloride (Zn). The synthesized compounds were characterized by FTIR and NMR spectroscopy and by X-ray diffraction on single crystal. The compounds were preliminary screened for their antibacterial and antifungal activity and the obtained results are very promising. In this respect, the hybrid -(quinolin-8-yl)-4-chloro-benzenesulfonamide cadmium (II), considered as leading structure for further studies, has an excellent antibacterial activity against (with a diameters of inhibition zones of 21 mm and a minimum inhibitory concentration (MIC) of 19.04 × 10 mg/mL), a very good antibacterial activity against (with a diameters of inhibition zones of 19 mm and a MIC of 609 × 10 mg/mL), and again an excellent antifungal activity against (with a diameters of inhibition zones of 25 mm and a MIC of 19.04 × 10 mg/mL).

摘要

设计、合成了两个新系列的混合喹啉-磺胺类配合物(M:Zn、Cu、Co 和 Cd)衍生物(),并测试了它们的抗菌活性。合成方法简单高效,包括两步:氨基喹啉的酰化反应,然后与金属醋酸盐(Cu、Co 和 Cd)或氯化物(Zn)络合。通过傅里叶变换红外光谱(FTIR)、核磁共振光谱(NMR)和单晶 X 射线衍射对合成的化合物进行了表征。对化合物进行了初步的抗菌和抗真菌活性筛选,结果非常有前景。在这方面,被认为是进一步研究的主导结构的混合-(8-喹啉基)-4-氯苯磺酰胺镉(II)对具有极好的抗菌活性(抑菌圈直径为 21mm,最小抑菌浓度(MIC)为 19.04×10mg/mL),对具有极好的抗菌活性(抑菌圈直径为 19mm,MIC 为 609×10mg/mL),对又具有极好的抗真菌活性(抑菌圈直径为 25mm,MIC 为 19.04×10mg/mL)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/f4f3f4c77f09/molecules-25-02946-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/a1ed7c1d2697/molecules-25-02946-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/84d8e0d95657/molecules-25-02946-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/f88c8e419163/molecules-25-02946-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/5ae44a1c7bcc/molecules-25-02946-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/8b220d3bb665/molecules-25-02946-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/8f16280eaa82/molecules-25-02946-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/f4f3f4c77f09/molecules-25-02946-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/a1ed7c1d2697/molecules-25-02946-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/84d8e0d95657/molecules-25-02946-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/f88c8e419163/molecules-25-02946-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/5ae44a1c7bcc/molecules-25-02946-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/8b220d3bb665/molecules-25-02946-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/8f16280eaa82/molecules-25-02946-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a21/7356327/f4f3f4c77f09/molecules-25-02946-g005.jpg

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