| Cat. No. |
Product Name |
Information |
| PC-20955 |
DHCR24 inhibitor SH42
|
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 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-20937 |
NV930
FTSJ1 inhibitor
|
NV930 is a small molecule inhibitor of tRNA-specific 2′-O-methyltransferase (FTSJ1), exerts readthrough activity in vitro and in vivo. |
| 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-20935 |
NV914
FTSJ1 inhibitor
|
NV914 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
|
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-20930 |
DLin-MC2-DMA
|
DLin-MC2-DMA is an ionizable lipid used for development of lipidoid nanoparticles for siRNA, mRNA, and vaccine delivery. |
| PC-20929 |
DLin-MC4-DMA
|
D-Lin-MC4-DMA is an ionizable lipid used for development of lipidoid nanoparticles for siRNA, mRNA, and vaccine delivery. |
| PC-20927 |
Cantrixil
CAS 2135511-22-5
|
Cantrixil (TRX-E-002-1) is a potent inducer of CD44+/MyD88+ ovarian cancer stem cell (OCSC) death with IC50 of 47 nM. |
| 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
|
TAK-831 (Luvadaxistat, NBI-1065844) is a highly potent, selective D-amino acid oxidase (DAAO) inhibitor with IC50 of 14 nM against human recombinant DAAO enzyme. |
