Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis

The obligate intracellular bacterium Chlamydia trachomatis is a group of worldwide human pathogens that can lead to serious reproductive problems. The frequent clinical treatment failure promoted the development of novel antichlamydial agents. Here, we firstly reported a group of pyrroloisoxazolidin...

Full description

Bibliographic Details
Main Authors: Min Ni, Shunxin Xu, Ziyi Liu, Yin Xue, Wenxia Xie, Shengju Yang, Lingyan Liu, Xiaofeng Bao
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2021/8889247
id doaj-24a4021da9f340dc9d60eba1ed757ebb
record_format Article
spelling doaj-24a4021da9f340dc9d60eba1ed757ebb2021-03-29T00:08:47ZengHindawi LimitedBioMed Research International2314-61412021-01-01202110.1155/2021/8889247Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatisMin Ni0Shunxin Xu1Ziyi Liu2Yin Xue3Wenxia Xie4Shengju Yang5Lingyan Liu6Xiaofeng Bao7School of PharmacySchool of PharmacySchool of PharmacySchool of PharmacySchool of PharmacyDepartment of Dermatology and VenereologyState Key Laboratory of Elemento-Organic ChemsitrySchool of PharmacyThe obligate intracellular bacterium Chlamydia trachomatis is a group of worldwide human pathogens that can lead to serious reproductive problems. The frequent clinical treatment failure promoted the development of novel antichlamydial agents. Here, we firstly reported a group of pyrroloisoxazolidine-inhibited C. trachomatis in a dose-dependent manner in vitro. Among them, compounds 1 and 2 exhibited the strongest inhibitory activity with IC50 values from 7.25 to 9.73 μM. The compounds disturbed the whole intracellular life cycle of C. trachomatis, mainly targeting the middle reticulate body proliferation stages. Besides, the compounds partially inhibited the chlamydial infection by reducing elementary body infectivity at high concentration. Our findings suggest the potential of pyrroloisoxazolidine derivatives as promising lead molecules for the development of antichlamydial agents.http://dx.doi.org/10.1155/2021/8889247
collection DOAJ
language English
format Article
sources DOAJ
author Min Ni
Shunxin Xu
Ziyi Liu
Yin Xue
Wenxia Xie
Shengju Yang
Lingyan Liu
Xiaofeng Bao
spellingShingle Min Ni
Shunxin Xu
Ziyi Liu
Yin Xue
Wenxia Xie
Shengju Yang
Lingyan Liu
Xiaofeng Bao
Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
BioMed Research International
author_facet Min Ni
Shunxin Xu
Ziyi Liu
Yin Xue
Wenxia Xie
Shengju Yang
Lingyan Liu
Xiaofeng Bao
author_sort Min Ni
title Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
title_short Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
title_full Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
title_fullStr Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
title_full_unstemmed Inhibitory Activity of Pyrroloisoxazolidine Derivatives against Chlamydia trachomatis
title_sort inhibitory activity of pyrroloisoxazolidine derivatives against chlamydia trachomatis
publisher Hindawi Limited
series BioMed Research International
issn 2314-6141
publishDate 2021-01-01
description The obligate intracellular bacterium Chlamydia trachomatis is a group of worldwide human pathogens that can lead to serious reproductive problems. The frequent clinical treatment failure promoted the development of novel antichlamydial agents. Here, we firstly reported a group of pyrroloisoxazolidine-inhibited C. trachomatis in a dose-dependent manner in vitro. Among them, compounds 1 and 2 exhibited the strongest inhibitory activity with IC50 values from 7.25 to 9.73 μM. The compounds disturbed the whole intracellular life cycle of C. trachomatis, mainly targeting the middle reticulate body proliferation stages. Besides, the compounds partially inhibited the chlamydial infection by reducing elementary body infectivity at high concentration. Our findings suggest the potential of pyrroloisoxazolidine derivatives as promising lead molecules for the development of antichlamydial agents.
url http://dx.doi.org/10.1155/2021/8889247
work_keys_str_mv AT minni inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT shunxinxu inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT ziyiliu inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT yinxue inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT wenxiaxie inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT shengjuyang inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT lingyanliu inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
AT xiaofengbao inhibitoryactivityofpyrroloisoxazolidinederivativesagainstchlamydiatrachomatis
_version_ 1714761195643207680