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Cat. No. Product Name Information
PC-20964

DX2-201

OXPHOS complex I inhibitor

DX2-201 is a potent and selective oxidative phosphorylation (OXPHOS) complex I inhibitor with IC50 of 312 nM in NAD/NADH 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.
PC-20890

Lalistat-1

LAL inhibitor

Lalistat 1 is a potent and selective lysosomal acid lipase (LAL) inhibitor with IC50 of 68 nM, shows no significant activity against pancreatic lipase or lipoprotein lipase.

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