AMP |
adenosine monophosphate |
ATP |
adenosine triphosphate |
CA |
carbonic anhydrase |
Dev/DosR |
DevR/DosR dormancy regulator |
DMAD |
dimethyl acetylenedicarboxylate |
DNA |
deoxyribonucleic acid |
DprE1 |
decaprenylphosphoryl-β-D-ribose 2′-oxidase |
FadD32 |
fatty acid degradation protein D32 |
FICI |
fractional inhibitory concentration index |
HadAB |
(3R)-hydroxyacyl-ACP dehydratase heterodimer |
HEK-293 |
human embryonic kidney cell line |
HIV |
human immunodeficiency virus |
IC50
|
half maximal inhibitory concentration |
InhA |
enoyl-acyl carrier protein reductase |
KasA |
β-ketoacyl-acyl carrier protein synthase |
Ki |
inhibition constant |
MDR |
multidrug-resistant |
MIC |
minimum inhibitory concentration |
MmpL3 |
mycobacterial membrane protein large 3 |
MptpA |
Mycobacterium tuberculosis protein tyrosine phosphatase A |
MptpB |
Mycobacterium tuberculosis protein tyrosine phosphatase B |
Mtb |
Mycobacterium tuberculosis |
MurB |
UDP-N-acetylenolpyruvoylglucosamine reductase |
Pks13 |
polyketide synthase |
PS |
pantothenate synthetase |
PTP1B |
protein tyrosine phosphatase 1B |
QSAR |
quantitative structure–activity relationship |
RAW 264.7 |
adherent cell line isolated from a mouse tumor that was induced by Abelson murine leukemia virus |
SAR |
structure–activity relationship |
TB |
tuberculosis |
THF |
tetrahydrofuran |
TZD |
thiazolidine-2,4-dione |
XDR |
extensively drug-resistant |
Zmp1 |
zinc metalloprotease 1 |