| Cat. No. |
Product Name |
Information |
| PC-24832 |
TPN-0157345
MmpL3 inhibitor
|
TPN-0157345 is a small molecule inhibitor of Mycobacterium tuberculosis (M.tb) mycolic acid exporter MmpL3, targets cell wall biosynthesis, inhibits aerobically cultured M. tuberculosis H37Rv with IC90 of 3.3 uM. |
| PC-24816 |
DRILS-1398
M.tb chorismate mutase inhibitor
|
DRILS-1398 is a potent inhibitor of M.tb chorismate mutase (M.tb-CM) with IC50 of 3.0 uM, demonstrates efficacy against multi-drug resistant M.tb strains (MIC=4 ug/mL), inhibits M.tb amino acid biosynthetic pathway. |
| PC-24738 |
Tarocin B
TarO inhibitor
|
Tarocin B is a specific inhibitor of UDP-N-acetylglucosamine-undecaprenyl-phosphate N-acetylglucosaminephosphotransferase (TarO) with IC50 of 0.41 uM, inhibits the first step in wall teichoic acid biosynthesis, restore β-lactam efficacy against MRSA. |
| PC-24471 |
TU-514
LpxC inhibitor
|
TU-514 is a substrate-analog inhibitor of zinc-dependent UDP-3-O-acyl-N-acetylglucosamine deacetylase (LpxC) with Ki of 3.9 uM for E. coli LpxC and IC50 of 7.0 uM (A. aeolicus LpxC) |
| PC-24470 |
L-573655
LpxC inhibitor
|
L-573655 (L-573,655) is a specific small molecule inhibitor of UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC), inhibits E. coli LpxC with Ki values of 24 uM and approximately 50 nM, respectively. |
| PC-24466 |
JSF-4536
M.tb MenG inhibitor
|
JSF-4536 is a small molecule inhibitor of Mycobacterium tuberculosis methyltransferase MenG enzyme, inhibits menaquinone biosynthetic pathway, inhibits M. tuberculosis H37Rv strain with MIC of 0.78 uM. |
| PC-24465 |
JSF-4898
M.tb MenG inhibitor
|
JSF-4898 is a small molecule inhibitor of Mycobacterium tuberculosis methyltransferase MenG enzyme, inhibits menaquinone biosynthetic pathway, inhibits M. tuberculosis H37Rv strain with MIC of 0.78 uM. |
| PC-24460 |
IP6C
Type II Thoeris system inhibitor
|
IP6C is a small molecule inhibitor of type II Thoeris systems encoded by multiple bacteria species, inhibits BaY2 Thoeris with IC50 of 10 uM, inhibits the type II Thoeris system by blocking His-ADPR production by ThsB. |
| PC-24393 |
FG-2101
LpxC inhibitor
|
FG-2101 (FG2101) is a potent, in vivo active, non-hydroxamate inhibitor of LpxC with IC50 of 1 nM, exhibits exquisite selectivity over other bacterial and human metalloenzymes (>10,000-fold). |
| PC-24388 |
MBX-4132
Trans-translation inhibitor
|
MBX-4132 is a trans-translation inhibitor with IC50 of 0.6 uM and 0.4 uM in E. coli luciferase reporter assay and in vitro reconstituted assays respectively, exhibits potent broad-spectrum antibiotic activity against Gram-positive species and many Gram-negative species. |
| PC-24353 |
H052
S. aureus α-hemolysin inhibitor
|
H052 is a highly potent S. aureus α-hemolysin (Hla) inhibitor, protect U937 cells from Hla-induced Ca2+ influx with EC50 of 0.01 uM, restores Hla-induced damage of host cell integrity. |
| PC-24346 |
NCBP1
Antibacterial
|
NCBP1 is a plant-derived, 11 amino acid, noncanonical antibacterial peptide with dual activity against multidrug-resistant bacterial and fungal pathogens, by targeting phosphatidylglycerol and cardiolipin in bacterial membrane, resulting in membrane damage and dysfunction. |
