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从一系列抗菌天然化合物中寻找针对新德里金属β-内酰胺酶1的潜在抑制剂。

Search of potential inhibitor against New Delhi metallo-beta-lactamase 1 from a series of antibacterial natural compounds.

作者信息

Thakur Prasoon Kumar, Kumar Jitender, Ray Divya, Anjum Farah, Hassan Md Imtaiyaz

机构信息

Department of Computer Science, Jamia Millia Islamia, New Delhi, India.

出版信息

J Nat Sci Biol Med. 2013 Jan;4(1):51-6. doi: 10.4103/0976-9668.107260.

Abstract

BACKGROUND

New Delhi metallo-β-lactamase-1 (NDM-1)-producing Gram-negative bacteria are today's major worldwide health concern. The enzyme NDM-1 provides bacterial resistance by its hydrolytic activity against the β-lactam ring of antibiotics. Inhibition of NDM-1 may prevent the hydrolysis of β-lactam ring of the antibiotics, and therefore, plays an important role against antibacterial resistance.

MATERIALS AND METHODS

Here we made an attempt to design suitable inhibitors against NDM-1 from different natural antibacterial compounds using molecular docking approach.

RESULTS

We observed that natural compounds such as Nimbolide and Isomargololone are showing an appreciable IC50 value as well as significant binding energy value for NDM-1. We further observed these compounds showing better affinity to NDM-1 on comparison with 14 β-lactam antibiotics.

CONCLUSION

Finally, our study provides a platform for the development of a potent inhibitor of NDM-1, which may be considered as a potential drug candidate against bacterial resistance.

摘要

背景

产新德里金属β-内酰胺酶-1(NDM-1)的革兰氏阴性菌是当今全球主要的健康关注点。NDM-1酶通过其对抗生素β-内酰胺环的水解活性赋予细菌耐药性。抑制NDM-1可能会阻止抗生素β-内酰胺环的水解,因此在对抗细菌耐药性方面发挥重要作用。

材料与方法

在此,我们尝试使用分子对接方法从不同的天然抗菌化合物中设计出适合的NDM-1抑制剂。

结果

我们观察到,诸如印楝素和异玛果龙醇等天然化合物对NDM-1显示出可观的半数抑制浓度(IC50)值以及显著的结合能值。我们进一步观察到,与14种β-内酰胺抗生素相比,这些化合物对NDM-1表现出更好的亲和力。

结论

最后,我们的研究为开发一种有效的NDM-1抑制剂提供了一个平台,该抑制剂可被视为一种潜在的抗细菌耐药性候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1c0/3633303/40886efade2c/JNSBM-4-51-g002.jpg

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