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. 2024 Jun 18;77(9):577–588. doi: 10.1038/s41429-024-00750-2

Table 2.

Antibacterial susceptibility (MIC, µg ml−1), efflux ratios, and ribosomal affinity IC50 (µM) against Mycobacterial species

M. tuberculosis H37Rv M. abscessus ATCC 19977 M. smegmatisa
Compound WT MIC (µg ml−1) ∆1258c MIC (µg ml−1) Efflux Ratio WT MIC (µg ml−1) ∆2780c MIC (µg ml−1) Efflux Ratio WT MIC (µg ml-1) Ribo. IC50 (µM)
SPC (1) 64 4 16 512 16 32 64 0.80b
TroSPC (2) 32 2 16 64 16 4 32 0.51
SPA (3) 2 4 0.5 64c 16c 4c ND 1.80d
TroSPA (4) 2 1 2 64 16 4 32 2.45
bAmSPC (5) 16 2 8 128 8 16 ND 1.18b
bAmTroSPC (6) 8 1 8 64 64 1 64 2.49
eAmSPC (7) 2 0.5 4 4 1 4 4 1.01b
eAmTroSPC (8) 2 0.25 8 8 8 1 8 2.31
Amino TroSPC (11) 16 2 8 64 64 1 32 0.64
AmTroSPC (13) 64 8 8 64 64 1 128 2.71

aMIC assays were conducted using M. smegmatis strain MC2 155. Ribosome inhibition assays were conducted using ribosomes purified from M. smegmatis strain SZ380

bRibosomal IC50 for compounds 1, 5, and 7 were previously reported in ref. [20]

cLead SPA 1810 (Compound 39 from ref. [16]) was substituted for SPA 3. SPA 1810 possess an additional hydroxyl on the para position of the pyridine ring when compared to SPA 3

dRibosomal IC50 used for compound 3 was converted from µg/mL to µM from what was previously reported in ref. [16]