| Cat. No. |
Product Name |
Information |
| PC-21015 |
YB-537
Quinone reductase 2 inhibitor
|
YB-537 (YB537) is a potent, highly specific quinone reductase 2 (QR2) inhibitor with IC50 of 3 nM, shows no activity against QR1 (IC50>10 uM). |
| PC-21002 |
FDW028
FUT8 inhibitor
|
FDW028 is a potent and highly selective small-molecule inhibitor of fucosyltransferase 8 (FUT8) with binding KD value of 5.486 uM, displays no affinity against other FUTs, shows potent anti-CRC activities. |
| PC-20988 |
Tax-1-hDLG1 inhibitor 3
Tax-1-hDLG1 inhibitor
|
Tax-1-hDLG1 inhibitor 3 (iTax/PDZ-01) is a small molecule inhibitor of Tax-1-hDLG1 interaction with EC50 of 11.5 uM, blocks HTLV-1 cell to cell transmission and viral replication. |
| PC-20977 |
ZINC549719643
AmpC β-lactamase inhibitor
|
ZINC549719643 is a highly potent inhibitor of AmpC β-lactamase with IC50 of 77 nM. |
| PC-20955 |
DHCR24 inhibitor SH42
DHCR24 inhibitor
|
DHCR24 inhibitor SH42 is a potent, selective, non-toxic delta 24-dehydrocholesterol reductase (DHCR24, Seladin-1) inhibitor, inhibits overall cholesterol biosynthesis in HL-60 cells with IC50 of 4.2 nM. |
| PC-20946 |
PSF-RNA inhibitor C-65
PSF-RNA inhibitor
|
PSF-RNA inhibitor C-65 is a small molecule inhibitor of RNA-binding protein PSF and its target RNA with IC50 of 0.02 uM in pull-down assays. |
| PC-20936 |
NV848
FTSJ1 inhibitor
|
NV848 is a small molecule inhibitor of tRNA-specific 2′-O-methyltransferase (FTSJ1), exerts readthrough activity in vitro and in vivo. |
| PC-20933 |
GSK898
KMO inhibitor
|
GSK898 is a potent, highly selective kynurenine monooxygenase (KMO) inhibitor with pIC50 of 8.8. |
| PC-20931 |
CIN-16645
Cationic lipid
|
CIN-16645 (LP-01) is an ionizable cationic amino lipid used in combination with other lipids in the formation of lipid nanoparticles (LNPs) to deliver single-guide RNA (sgRNA) targeting MHC class II transactivator (CIITA) in T cells. |
| PC-20910 |
MC-1-F2
FOXC2 inhibitor
|
MC-1-F2 is the first inhibitor of forkhead box protein C2 (FOXC2) with Kd of 26 uM, induces cadherin switching and reverses EMT through the degradation of FOXC2, blocks FOXC2 nuclear localization. |
| PC-20909 |
GPR56 agonist 36
GPR56 agonist
|
GPR56 agonist 36 is a potent selective agonist of adhesion GPCR ADGRG1/GPR56 with EC50 of 2.95 uM. |
| PC-20902 |
Luvadaxistat
DAAO inhibitor
|
Luvadaxistat (TAK-831, NBI-1065844) is a highly potent, selective D-amino acid oxidase (DAAO) inhibitor with IC50 of 14 nM against human recombinant DAAO enzyme. |
