2019
DOI: 10.1039/c8ob03109f
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Synthesis, bioactivity, and enzymatic modification of antibacterial thiotetromycin derivatives

Abstract: Interrogating the bioactivities and enzymatic modification potential of a focused library of novel synthetic thiotetronate compounds.

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Cited by 5 publications
(2 citation statements)
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References 46 publications
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“…YD also reversed NNMT-mediated resistance of non-small cell lung cancer cells to 5-FU [124]. The anti-bacterial compound thiotetramycin and its derivatives demonstrated mild inhibitory effects against NNMT [212]. JBSNF-000088 (a substrate inhibitor) [201,202], 6-methylaminonicotinamide [213] and methylated quinolinium analogues such as 5-amino-1-methylquinoline [34,214], are nicotinamide analogues which all have IC 50 values in the single µM range.…”
Section: Nicotinamide Analoguesmentioning
confidence: 99%
“…YD also reversed NNMT-mediated resistance of non-small cell lung cancer cells to 5-FU [124]. The anti-bacterial compound thiotetramycin and its derivatives demonstrated mild inhibitory effects against NNMT [212]. JBSNF-000088 (a substrate inhibitor) [201,202], 6-methylaminonicotinamide [213] and methylated quinolinium analogues such as 5-amino-1-methylquinoline [34,214], are nicotinamide analogues which all have IC 50 values in the single µM range.…”
Section: Nicotinamide Analoguesmentioning
confidence: 99%
“…13). 104,105 The tlm gene cluster was then heterologously expressed in Streptomyces coelicolor using a TAR cloning strategy, which resulted in the identification of thiolactomycin and three new analogues. Later, mutagenesis and comparative metabolic analyses revealed the involvement of tlmF-tlmI genes in the γ-thiolactone skeleton construction of this class of antibiotics.…”
Section: Thiolactomycin and Thiotetromycinsmentioning
confidence: 99%