Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Xiudong Ding"'
Autor:
Ying Jiang, Xinqiang Zhang, Bo Wang, Liping Tang, Xin Liu, Xiudong Ding, Yueming Dong, Hong Lei, Di Wang, Huicheng Feng
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-14 (2024)
Abstract Background Cell subsets differentially modulate host immune responses to Mycobacterium tuberculosis (MTB) infection. However, the nature and functions of these subsets against osteoarticular tuberculosis (OTB) are unclear. Here, we aimed to
Externí odkaz:
https://doaj.org/article/a8ff9f2ef337405f90ab3d1817fdc224
Autor:
Yinliang Qi, Xiudong Ding, Kun Wang, Pingzhen Yan, Xinxin Guo, Shiwei Ma, Mingfei Xiao, Pengrui Sun, Siyu Liu, Yunlei Hou, Yanfang Zhao
Publikováno v:
New Journal of Chemistry. 46:9470-9485
A series of new biaryloxazolidinone derivatives has been designed and synthesized using the combination principle and blocking metabolic site to improve their antibacterial activity and stability.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::625a02f60575ba2a56790f24fea21c67
https://doi.org/10.1039/d2nj00479h
https://doi.org/10.1039/d2nj00479h
Autor:
Yunlei Hou, Xiudong Ding, Zhanfeng Gao, Siyu Liu, Sicong Xu, Zhiwei Li, Jia Jiang, Ruixi Fan, Tong Chen, Yanfang Zhao, Hengzhi Lu
Publikováno v:
Letters in Drug Design & Discovery. 20
Background: In this article, a series of novel oxazolidinone derivatives containing dithiocarbamate moieties have been designed and synthesized. Methods: Their antibacterial activities were measured against Staphylococcus aureus, vancomycin-resistant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88cfa7108b8778d56320e154e7edc702
https://doi.org/10.2174/1570180820666230118124058
https://doi.org/10.2174/1570180820666230118124058
Publikováno v:
Japanese Journal of Infectious Diseases. 74:245-248
Through our previous work, we have identified that novel oxazolidinone structures, the biaryloxazolidinone analogues containing a hydrazone moiety, act as promising antibacterial agents against gram-positive bacterial strains. Based on this active st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e5b03a6c44cceccae74694356ab92f3
https://doi.org/10.7883/yoken.jjid.2020.307
https://doi.org/10.7883/yoken.jjid.2020.307
Autor:
Xiudong Ding, Zhanfeng Gao, Siyu Liu, Yu Wang, Shihui Wang, Sicong Xu, Zhiwei Li, Jia Jiang, Ruixi Fan, Tong Chen, Yanfang Zhao, Hengzhi Lu, Yunlei Hou
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ac51626096e4f15d01f019ea4b0afd
https://doi.org/10.2139/ssrn.4129776
https://doi.org/10.2139/ssrn.4129776
Autor:
Zengkui Yan, Xue Mei, Ying Jiang, Jing Zhou, Yinghui Chai, Xiudong Ding, Xin Liu, Hong Lei, Yueming Dong
Publikováno v:
Microbes and Infection. 24:104893
BACKGROUND There is an abundant link between the gut microbiota and human health and it plays a critical role in the clinic. It is recognized that microbial dysregulation contributes to the pathogenesis of tuberculosis (TB), but the underlying mechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a64f24812210a51944eccaaa9f91d42
https://doi.org/10.1016/j.micinf.2021.104893
https://doi.org/10.1016/j.micinf.2021.104893
Publikováno v:
Bioorganicmedicinal chemistry letters. 32
A series of novel oxazolidinone derivatives with nitrogen-containing fused heterocyclic moiety were designed and synthesized in this article. Their antibacterial activities were measured against S. aureus, MRSA and MSSA by MIC assay. Most of them exh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34456e87e75c7778f4e57c2183ef9c65
https://pubmed.ncbi.nlm.nih.gov/33144245
https://pubmed.ncbi.nlm.nih.gov/33144245
Publikováno v:
Chemical Research in Chinese Universities. 34:51-56
A series of novel oxazolidinone derivatives containing nitro heteroaromatic moiety was synthesized and characterized by means of 1H NMR and MS spectra. All target compounds were evaluated for their in vitro antibac-terial activities against S.au 2921
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a70d37184ee6b959746b344c8678626
https://doi.org/10.1007/s40242-018-7302-3
https://doi.org/10.1007/s40242-018-7302-3
Autor:
Yinliang Qi, Yifeng Yang, Yanfang Zhao, Yingxiu Li, Xiudong Ding, Mingze Qin, Lu Sun, Feng Hu, Yajing Liu, Yachuang Wu
Publikováno v:
European Journal of Medicinal Chemistry. 185:111781
We previously discovered a series of novel biaryloxazolidinone analogues bearing a hydrazone moiety with potent antibacterial activity. However, the most potent compound OB-104 exhibited undesirable chemical and metabolic instability. Herein, novel b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8777bcf5c20b170ad9ec472910e1f15
https://doi.org/10.1016/j.ejmech.2019.111781
https://doi.org/10.1016/j.ejmech.2019.111781
Autor:
Xue Zhang, Yanfang Zhao, Sicong Xu, Xiudong Ding, Chu Wang, Hong Lei, Yifeng Yang, Yachuang Wu
Publikováno v:
Bioorganicmedicinal chemistry letters. 29(3)
Novel biaryloxazolidinone derivatives containing a rhodanine or thiohydantoin moiety were designed, synthesized and evaluated for their antibacterial activity. The key compounds 7 and 9 were synthesized by the knoevenagel condensation of intermediate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30911a9dac472a1a6baec3735758afa8
https://pubmed.ncbi.nlm.nih.gov/30553735
https://pubmed.ncbi.nlm.nih.gov/30553735