| Cat. No. |
Product Name |
Information |
| PC-26316 |
VRK1 inhibitor Compound 1
VRK1 inhibitor
|
VRK1 inhibitor Compound 1 (VRK1-IN-1) is a potent, selective and ATP-competitive inhibitor of Vaccinia-related kinase 1 (VRK1) with Ki of 82 nM and IC50 of 154 nM, selective for VRK1 over VRK2. |
| PC-26307 |
JX24120
MAT2B inhibitor
|
JX24120 is a specific inhibitor for methionine adenosyltransferase MAT2B, directly binds to MAT2B with SPR KD of 4.72 uM, inhibits S-adenosylmethionine (SAMe) synthesis. |
| PC-26291 |
UNC11676A
MDA5 inhibitor
|
UNC11676A is a specific small molecule inhibitor of RNA helicase MDA5 with IC50 of 6 uM, >18-fold selective inhibition over LGP2 and DDX1. |
| PC-26266 |
CVN14
CD38 inhibitor
|
CVN14 is a potent, selective, uncompetitive and brain-penetrant CD38 inhibitor with IC50 of 19 nM and 2 nM for human and mouse CD38 respectively. |
| PC-26242 |
E8431
DCSTAMP antagonist
|
E8431 (Z2371498431) is a specific small molecule antagonist of fusogenic protein DCSTAMP, disrupts DCSTAMP-RAP1B interaction and inhibits RAP1-RAC1 signaling-mediated cytoskeletal reorganization required for osteoclast maturation and fusion, demonstrats significant osteoclastogenesis inhibition (IC50=0.7758 μM) without cytotoxic effects on mBMMs. |
| PC-26237 |
HF13141-H5
GGCX inhibitor
|
HF13141-H5 is a potent, selective inhibitor of γ-Glutamyl carboxylase (GGCX) with IC50 of 240 nM-1 uM in cell-based assays, inhibits γ-carboxylation of vitamin K-dependent clotting factors (VKDCFs) and shows anticoagulant effect. |
| PC-26220 |
Thiostrepton
FOXM1 inhibitor, PRX3 inhibitor
|
Thiostrepton is a thiazole antibiotic that selectively inhibits FOXM1, also significantly inhibits ETV4 K97-Khib, thereby promoting ferroptosis and suppressing ICC cell migration, invasion, and lung metastasis, covalently inhibits Peroxiredoxin 3 (PRX3), disrupting redox balance and selectively induces tumor cell death. |
| PC-26205 |
CN-0928
PCBP2 inhibitor
|
CN-0928 is a specific small molecule inhibitor of poly(C)-binding protein 2 (PCBP2), mitigates AD pathology by inhibiting PCBP2 condensation. |
| PC-26181 |
CAPib-13
CAP-1 inhibitor
|
CAPib-13 is a small-molecule inhibitor of CAP-1 (cyclase-associated protein-1) with SPR KD of 2.57 uM, significantly suppresses colorectal cancer metastasis. |
| PC-26148 |
NFAT Inhibitor VIVIT peptide
NFAT inhibitor
|
NFAT Inhibitor VIVIT peptide is a peptide inhibitor of nuclear factor of activated Tcells (NFAT), selectively inhibits calcineurin-mediated dephosphorylation of NFAT. |
| PC-26147 |
A-285222
NFAT inhibitor
|
A-285222 (A-285) is a bis-trifluoromethyl-pyrazole (BTP) and selective nuclear factor of activated T cells (NFAT) inhibitor, inhibits PBMC proliferation stimulated by concanavalin A with IC50 of 146 nM, inhibits IL-2 synthesis in human blood with IC50 of 182 nM. |
| PC-26146 |
INCA-6
NFAT inhibitor
|
INCA-6 (Inhibitor of NFAT-calcineurin association 6) is a specific, cell-permeable nuclear factor of activated T cells (NFAT) inhibitor, binds to calcineurin with high affinity (KD=0.8 uM) and specifically disrupts its interaction with NFAT. |
