| Cat. No. |
Product Name |
Information |
| PC-23722 |
QP5020
QPCTL inhibitor
|
QP5020 is a potent inhibitor of glutaminyl-peptide cyclotransferase-like protein (QPCTL) with IC50 of 15 nM. |
| PC-23697 |
Neocarzilin A
VAT1 inhibitor
|
Neocarzilin A (NCA) is a potent inhibitor of cancer cell migration, irreversibly binds to and inhibits the synaptic vesicle membrane protein VAT-1. |
| PC-23649 |
Genipin
UCP2 inhibitor
|
Genipin is a specific small molecule inhibitor of uncoupling protein 2 (UCP2), inhibits UCP2-mediated mitochondrial proton leak. |
| PC-23604 |
CCG257081
MRTF/SRF inhibitor
|
CCG-257081 is a small molecule MRTF/SRF pathway inhibitor, shows direct binding to pirin with ITC KD value of 8.6 uM, inhibits melanoma metastasis and bleomycin-induced fibrosis. |
| PC-23580 |
Licochalcone C
α-glycosidase inhibitor
|
Licochalcone C is a selective inhibitor of α-glycosidase with IC50 of <100 nM, does not inhibit PTP1B, induces apoptosis via Bcl-2 family proteins in T24 cells. |
| PC-23578 |
Licochalcone A
UGT inhibitor
|
Licochalcone A is a broad-spectrum inhibitor of UDP-glucuronosyltransferase (UGT) with IC50/Ki values of <5 uM for UGT1A1、1A3、1A4、1A6、1A7、1A9 and 2B7, shows anti-cancer effects, |
| PC-23556 |
Purpurin
GDH1 inhibitor
|
Purpurin is a potent, specific inhibitor of glutamate dehydrogenase 1 (GDH1/GLUD1) with Ki of 1.9 uM, inhibits cancer cell proliferation and tumor growth. |
| PC-23544 |
LH1513
CaOx crystallization inhibitor
|
LH1513 (L-Lysine Dioxalate) is potent inhibitor of calcium oxalate (CaOx) crystallization with EC50 of 21.7 uM. |
| PC-23540 |
FPD5
Esterase D inhibitor
|
FPD5 is a small molecule activator of esterase D (ESD) with KD value of 0.8 nM, directly binds to ESD at Lys180 rather than its ubiquitination site Lys213. |
| PC-23538 |
WYFA15
SMS1 inhibitor
|
WYFA15 is a small molecule inhibitor of sphingomyelin synthase 1 (SMS1), inhibits severe fever with thrombocytopenia syndrome virus (SFTSV) infection and reduces SARS-CoV-2 replication and pathogenesis. |
| PC-23520 |
Warfarin
VKORC1L1 inhibitor
|
Warfarin (WARF-42, Athrombine-K) is a potent anticoagulant agent and a vitamin K1 recycling antagonist to deplete active vitamin K1, is a small molecular inhibitor of vitamin K epoxide reductase complex subunit 1 like 1 (VKORC1L1). |
| PC-23516 |
BC-DXI-843
AIMP2-DX2 inhibitor
|
BC-DXI-843 is a potent and specific AIMP2-DX2 inhibitor with IC50 og 0.92 uM, >100-fold selectivity over AIMP2. |
