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Cat. No. Product Name Information
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-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.
PC-20842

GCN2iA

GCN2 inhibitor

GCN2iA is a potent seletive inhibitor of general control nonderepressible 2 (GCN2) with IC50 of 4.0 nM.
PC-20837

SRP-001

Analgesic agent

SRP-001 is a non-opioid and non-hepatotoxic small molecule ApAP analog, induces analgesia via N-arachidonoylphenolamine (AM404) formation, and generates higher amounts of AM404 than ApAP.
PC-20825

eEF-2K inhibitor 2C

eEF-2K inhibitor

eEF-2K inhibitor 2C (Compound 2C) is a small molecule inhibitor of eukaryotic elongation factor 2 kinase (eEF-2K), binds to the ATP-binding site of eEF-2K.
PC-20821

PKA inhibitor H89

PKA inhibitor

PKA inhibitor H89 (H-89 dihydrochloride) is a potent, selective cAMP-dependent protein kinase A (PKA) inhibitor with IC50 of 48 nM, weakly inhibits PKG, PKC, casein kinases.
PC-20817

KZR-8445

Sec61 inhibitor

KZR-8445 (KZR8445) is a cyclic depsipeptide, client-selective Sec61 inhibitor with IC50 of 100 nM, targets the Sec61 translocon and selectively modulate Sec61-mediated protein biogenesis.
PC-20788

NSC348884

Nucleophosmin inhibitor

NSC348884 is a small molecule nucleophosmin (NPM) inhibitor, disrupts the formation of dimers and inhibits aberrant NPM functionin cancer cells.
PC-20785

Sodium phytate

Sodium phytate (Phytic acid sodium salt, InsP6 sodium) is the most abundant inositol phosphate in cells, is a strong inhibitor of iron absorption from fortified foods, has antioxidant and anti-diabetic properties.
PC-20779

HP661

OXPHOS inhibitor

HP661 is a potent, and selective oral complex I OXPHOS inhibitor with 76% inhibition at 1u M in H460 cells using electron flow assays, inhibits high-OXPHOS H460 cell viability with IC50 of 5 nM.

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