| Cat. No. |
Product Name |
Information |
| PC-26113 |
JZ128
PKN3 inhibitor
|
JZ128 is a selective, covalent inhibitor of Protein Kinase N3 (PKN3) with IC50 of 120 nM, targets Cys840 in PKN3, has no activity against CDK7 or CDK12/13. |
| PC-26095 |
Profilin1 inhibitor UP-6
Profilin1 inhibitor
|
Profilin1 inhibitor UP-6 is a specific small molecule inhibitor of Actin-binding protein profilin1 (Pfn1), inhibits Pfn1-actin interaction and tumor angiogenesis. |
| PC-26091 |
Etoxazole
Acaricide
|
Etoxazole (YI-5301) is a highly effective acaricide that affects the nymphs, eggs, and larvae of spider mites by inhibiting chitin biosynthesis. |
| PC-26086 |
IDB-003
Translation inhibitor
|
IDB-003 is an orally active, unique context-dependent inhibitor of human translation that bind to the ribosome peptidyl transferase center (PTC) and inhibits elongation. |
| PC-26085 |
IDB-001
Translation inhibitor
|
IDB-001 is a small molecule, unique context-dependent inhibitor of human translation that bind to the ribosome peptidyl transferase center (PTC) and inhibits elongation. |
| PC-26079 |
TREM2 agonist S9
TREM2 agonist
|
TREM2 agonist S9 is a potent, small molecule Triggering receptor expressed on myeloid cells-2 (TREM2) agonist with MST binding KD of 0.95 uM. |
| PC-26078 |
HCY-NBD
GSTM2 stablizer
|
HCY-NBD is a small molecule stabilizer of Glutathione S-transferase Mu 2 (GSTM2), promotes sulfenylation at Cys174 of GSTM2 and inhibits its K48-linked ubiquitination at this residue, stabilizes GSTM2 protein levels. |
| PC-26063 |
Berberrubine chloride
TDP-43 aggregation inhibitor
|
Berberrubine chloride is an orally active metabolite of berberine, alleviates mucosal lesions and inflammation in mouse colitis models, inhibits TDP-43 aggregation and shows anti-inflammatory, anti-tumor, and antiviral activities. |
| PC-26054 |
AGS8-IN-1
AGS8 inhibitor
|
AGS8-IN-1 is a small molecule inhibitor of activator of G-protein signaling 8 (AGS8), effectively inhibits the formation of the AGS8-Gβγ complex, attenuates VEGF-induced phosphorylation of signaling molecules and inhibits tube formation and migration of HUVECs. |
| PC-25998 |
TMA Lyase inhibitor 7
TMA Lyase inhibitor
|
TMA Lyase inhibitor 7 is a highly potent, selective Trimethylamine (TMA) Lyase inhibitor with IC50 of 0.4 nM, significant reduces circulating trimethylamine oxide (TMAO) levels in vivo. |
| PC-25965 |
ML194
GPR35 antagonist
|
ML194 is a potent, selective GPR35 antagonist with IC50 of 160 nM, has >57-fold selectivity over GPR55 orphan receptor. |
| PC-25962 |
CVN527
GPR6 inverse agonist
|
CVN527 is a potent and selective, brain penetrant GPR6 inverse agonist, fully inhibits GPR6 with EC50 of 39.5 nM and 34 nM for mouse and human GPR6 in functional GPR6 cAMP HTRF cell -based assays. |
