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具有改善生物学特性的含四氢呋喃氨基酸的短杆菌肽 S 类似物。

Tetrahydrofuran amino acid-containing gramicidin S analogues with improved biological profiles.

作者信息

Pal Sudip, Singh Gajendra, Singh Shyam, Tripathi Jitendra Kumar, Ghosh Jimut Kanti, Sinha Sudhir, Ampapathi Ravi Sankar, Chakraborty Tushar Kanti

机构信息

Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow-226031, India.

出版信息

Org Biomol Chem. 2015 Jun 28;13(24):6789-802. doi: 10.1039/c5ob00622h.

Abstract

Gramicidin S (GS) is a cyclic cationic antimicrobial peptide (CAP) with a wide spectrum of antibiotic activities whose usage has been limited to topical applications owing to its cytotoxic side effects. We have synthesized tetrahydrofuran amino acid (Taa)-containing GS analogues, and we have carried out conformational analysis and explored their structure activity relationships by evaluating their antitubercular, antibacterial and cytotoxic properties. Two of these analogues showed impressive as well as selective activity against Mycobacterium tuberculosis (MTB) without toxicity towards mammalian Vero cells or human RBCs, and are promising as potential leads.

摘要

短杆菌肽S(GS)是一种具有广泛抗生素活性的环状阳离子抗菌肽(CAP),由于其细胞毒性副作用,其应用仅限于局部应用。我们合成了含四氢呋喃氨基酸(Taa)的GS类似物,并通过评估它们的抗结核、抗菌和细胞毒性特性进行了构象分析并探索了它们的构效关系。其中两种类似物对结核分枝杆菌(MTB)表现出令人印象深刻的选择性活性,对哺乳动物Vero细胞或人红细胞无毒性,有望成为潜在的先导化合物。

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