| Cat. No. |
Product Name |
Information |
| PC-24394 |
BCT1028
BLVRB inhibitor
|
BCT1028 is a potent, selective small molecule Biliverdin IXβ reductase (BLVRB) inhibitor with IC50 of 195 nM (50 uM BLVRB substrate DCPIP). |
| PC-24385 |
HEX-1
Pin1 inhibitor
|
HEX-1 is a valuable addition to the armamentarium against CRC, suppresses the proliferation of cancer cells and tumorigenesis via the inactivation and sensitization of PIN1. |
| PC-24382 |
MitoSNO
Mitochondria S-nitrosating agent
|
MitoSNO (mitochondria-targeted S-nitrosothiol) is a mitochondria-selective S-nitrosating agent, selectively S-nitrosates mitochondrial proteins. |
| PC-24354 |
Fisetin
NUF2 inhibitor, YBX-1 inhibitor, ACVR2A inhibitor
|
Fisetin is a small molecule inhibitor of NUF2, effectively inhibits PCa cell proliferation, also is an inhibitor of Y-box binding protein-1 (YB-1, YBX-1) activation, is also a potent activin type 2 receptor A (ACVR2A) inhibitor with IC50 of 0.27 uM, shows antioxidant, anticancer, neuroprotection effects. |
| PC-24318 |
LPHN2 inhibitor D11
LPHN2 inhibitor
|
LPHN2 inhibitor D11 is a reversible and selective inhibitor of mechanosensitive GPCR latrophilin 2 (LPHN2, ADGRL2), inhibits mechanosensitivity of LPHN2 in HEK293 cells with IC50 of 20 nM. |
| PC-24310 |
NFS1 inhibitor Compound 53
NFS1 inhibitor
|
NFS1 inhibitor Compound 53 is the first potent, selective inhibitor of human cysteine desulfurase (NFS1) with IC50 of 40.5 uM and Ki of 6.4 uM. |
| PC-24307 |
BPRPT0245
PTGR2 inhibitor
|
BPRPT0245 is a specific small-molecule inhibitor of prostaglandin reductase 2 (PTGR2) with IC50 of 8.92 nM, restores 15-keto-PGE2-dependent PPARγ trans-activation in HEK293T cells expressing recombinant PTGR2 with EC50 of 49.22 nM. |
| PC-24295 |
HOSU-53
DHODH inhibitor
|
HOSU-53 (JBZ-001) is a potent and selective inhibitor of DHODH with IC50 of 0.95 nM (hDHODH), exhibits potent antileukemic activity. |
| PC-24293 |
HypoxyStat
Hypoxia inducer
|
HypoxyStat is a small molecule that increase oxygen-hemoglobin binding affinity cause tissue hypoxia, binds hemoglobin, induces systemic hypoxia in mice breathing normoxic (21% O2) air. |
| PC-24261 |
SARM1 inhibitor NB-7
SARM1 inhibitor
|
SARM1 inhibitor NB-7 is a potent, selective and uncompetitive inhibitor of the nicotinamide adenine dinucleotide (NAD) hydrolase SARM1 with biochemical IC50 of 0.025 uM, and IC50 of 0.008 uM in SARM-induced cell-death rescue assays. |
| PC-24260 |
SARM1 inhibitor 7
SARM1 inhibitor
|
SARM1 inhibitor 7 is a potent, selective sterile alpha and TIR Motif Containing 1 (SARM1) inhibitor with biochemical IC50 of 0.3 uM (hSARM1). |
| PC-24230 |
Glycyrrhizin
HMGB1 inhibitor, EV-A71 inhibitor
|
Glycyrrhizin (NSC167409, Glycyrrhizic acid) is a direct HMGB1(high mobility group box 1) inhibitor, also is a specific inhibitor of EV-A71, blocks EV-A71 replication both in vivo and in vitro. |
