| Cat. No. |
Product Name |
Information |
| PC-38337 |
CH24H inhibitor 17
CH24H inhibitor
|
CH24H inhibitor 17 is a potent, highly selective, BBB permeable inhibitor of Cholesterol 24-hydroxylase (CH24H/CYP46A1) with IC50 of 8.5 nM. |
| PC-38326 |
DMT1 inhibitor 18a
DMT1 inhibitor
|
DMT1 inhibitor 18g is the most potent inhibitor of divalent metal transporter 1 (DMT1) with IC50 of 50 nM in calcein fluorescence assay.. |
| PC-38325 |
DMT1 inhibitor 14a
DMT1 inhibitor
|
DMT1 inhibitor 14a is a potent inhibitor of divalent metal transporter 1 (DMT1) with IC50 of 340 nM in calcein fluorescence assay. |
| PC-38324 |
DMT1 inhibitor 6b
DMT1 inhibitor
|
DMT1 inhibitor 6b is a potent inhibitor of divalent metal transporter 1 (DMT1) with IC50 of 80 nM in calcein fluorescence assay. |
| PC-38323 |
DMT1 inhibitor 18g
DMT1 inhibitor
|
DMT1 inhibitor 18g is the most potent inhibitor of divalent metal transporter 1 (DMT1) with IC50 of 20 nM in calcein fluorescence assay.. |
| PC-38320 |
msR4M-L1
MIF inhibitor
|
msR4M-L1 is a chemokine-selective CXCR4 ectodomain mimic that selectively binds to MIF (KD<40 nM) but not CXCL12 (>140-fold selectivity). |
| PC-38316 |
BNZ132-1
IL-2/IL-15 inhibitor
|
BNZ132-1 (QITISILSQINRVFHEKFI) is a specific peptide inhibitor for the IL-2/IL-15 subfamily, directly binds to the γc molecule (CD132). |
| PC-38315 |
BNZ-1
IL-2/IL-15 inhibitor
|
BNZ-1 (BNZ132-1-40) is a pegylated peptide, BNZ132-1 conjugated with methoxy-PEG40 maleimide molecule via a specific linker (CGSGG), specifically binds the γc receptor to selectively block IL-2, IL-15 and IL-9 signaling. |
| PC-38301 |
PRGL493
ACSL4 inhibitor
|
PRGL493 (PRGL 493) is a potent selective inhibitor of Acyl-CoA synthetase 4 (ACSL4). |
| PC-38288 |
Apostatin-1
TRADD inhibitor
|
Apostatin-1 is a small molecule that binds to a pocket on the N-terminal TRAF2-binding domain of TRADD (TRADD-N). |
| PC-38287 |
ICCB-19
TRADD inhibitor
|
ICCB-19 is a small molecule that binds to a pocket on the N-terminal TRAF2-binding domain of TRADD (TRADD-N). |
| PC-38284 |
LDC7559
PFKL activator
|
LDC7559 is a small molecule that efficiently blocks NET formation and GSDMD-mediated pyroptotic cell death in human cells, also is an inhibitor of NOX2-dependent NETosis. |
