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Cat. No. Product Name Information
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-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.
PC-20890

Lalistat-1

LAL inhibitor

Lalistat 1 (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.
PC-20889

Lalistat-2

LAL inhibitor

Lalistat-2 (L-stat, Lalistat 2) is a specific inhibitor of lysosomal acid lipase (LAL) with IC50 of 152 nM, shows no significant activity against pancreatic lipase or lipoprotein lipase.
PC-20847

C902

LIN28 inhibitor

C902 is a small-molecule inhibitor targeting LIN28-let-7 interaction, shows dose-dependent inhibition in an EMSA validation assay with IC50 of 5 uM.

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