Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/142311
Title: 1,3,5-triazaspiro[5.5]undeca-2,4-dienes as selective Mycobacterium tuberculosis dihydrofolate reductase inhibitors with potent whole cell activity
Authors: Yang, Xuan
Wedajo, Wassihun
Yamada, Yoshiyuki
Dahlroth, Sue-Li
Neo, Jason Jun-Long
Dick, Thomas
Chui, Wai-Keung
Keywords: Science::Biological sciences
Issue Date: 2018
Source: Yang, X., Wedajo, W., Yamada, Y., Dahlroth, S.-L., Neo, J. J.-L., Dick, T., & Chui, W.-K. (2018). 1,3,5-triazaspiro[5.5]undeca-2,4-dienes as selective Mycobacterium tuberculosis dihydrofolate reductase inhibitors with potent whole cell activity. European journal of medicinal chemistry, 144, 262-276. doi:10.1016/j.ejmech.2017.12.017
Journal: European journal of medicinal chemistry
Abstract: The emergence of multi- and extensively-drug resistant tubercular (MDR- and XDR-TB) strains of mycobacteria has limited the use of existing therapies, therefore new drugs are needed. Dihydrofolate reductase (DHFR) has recently attracted much attention as a target for the development of anti-TB agents. This study aimed to develop selective M. tuberculosis DHFR inhibitors using rationale scaffolding design and synthesis, phenotype-oriented screening, enzymatic inhibitory study, whole cell on-target validation, molecular modeling, and in vitro DMPK determination to derive new anti-TB agents. 2,4-diamino-1-phenyl-1,3,5-triazaspiro[5.5]undeca-2,4-dienes 20b and 20c were identified as selective M. tuberculosis DHFR inhibitors, showing promising antimycobacterial activities (MIC50: 0.01 μM and MIC90: 0.025 μM on M. tuberculosis H37Rv). This study provided compelling evidence that compound 20b and 20c exerted whole cell antimycobacterial activity through DHFR inhibition. In addition, these two compounds exhibited low cytotoxicity and low hemolytic activity. The in vitro DMPK and physiochemical properties suggested their potential in vivo efficacy.
URI: https://hdl.handle.net/10356/142311
ISSN: 0223-5234
DOI: 10.1016/j.ejmech.2017.12.017
Rights: © 2017 Elsevier Masson SAS. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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