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Cat. No. Product Name Information
PC-24908

LSN3441732

Lp(a) formation inhibitor

LSN3441732 is a potent, dimeric apolipoprotein(a) (apo(a)) binder and inhibitor of Lipoprotein(a) (Lp(a)) formation, disrupts the formation of Lp(a) with IC50 of 0.18 nM in in vitro Lp(a) assembly assays.
PC-24907

LSN3353871

Lp(a) formation inhibitor

LSN3353871 is a potent small-molecule apolipoprotein(a) (apo(a)) binder and inhibitor of Lipoprotein(a) (Lp(a)) formation, disrupts the formation of Lp(a) with IC50 of 1.69 uM in in vitro Lp(a) assembly assays.
PC-24905

IR-546

NIR fluorescent

IR-546 is a NIR fluorescent probe, inhibits melanoma cell proliferation by activating the mitochondrial apoptosis pathway through suppression of the AKT/GSK3β signaling pathway.
PC-24845

Sardomozide dihydrochloride

SAMDC inhibitor

SAM486A dihydrochloride (Sardomozide) is a highly potent, selective S-adenosylmethionine decarboxylase (SAMDC) inhibitor with IC50 of 5 nM, inhibits intracellular spermidine and spermine pools.
PC-24844

SAM486A

SAMDC inhibitor

SAM486A (Sardomozide) is a highly potent, selective S-adenosylmethionine decarboxylase (SAMDC) inhibitor with IC50 of 5 nM, inhibits intracellular spermidine and spermine pools.
PC-24839

NGI-186

Oligosaccharyltransferase inhibitor

NGI-186 is a potent, small molecule inhibitor of oligosaccharyltransferase (OST) with IC50 of 0.06 uM.
PC-24838

NGI-190

Oligosaccharyltransferase inhibitor

NGI-190 is a potent, small molecule inhibitor of oligosaccharyltransferase (OST) with IC50 of 0.59 uM.
PC-24837

NGI-189

Oligosaccharyltransferase inhibitor

NGI-189 is a potent, small molecule inhibitor of oligosaccharyltransferase (OST) with IC50 of 0.09 uM.
PC-24833

Pinosylvin

CAS 22139-77-1

Pinosylvin is a naturally occurring molecule traditionally found in pinus trees with antibacterial, antifungal and anticancer activity, shows potent growth inhibitory activity against Candida albicans and Saccharomyces cerevisiae.
PC-24820

KS122-0485428

Lysyl hydroxylase 2 inhibitor

KS122-0485428 is a specific small molecule inhibitor of Lysyl hydroxylase 2 (LH2), significantly enhances LH2 function in telopeptidyl Lys hydroxylation, cross-linking, and mineralization.
PC-24811

NSD-1015

AADC inhibitor

NSD-1015 (3-Hydroxybenzylhydrazine) is a specific small molecule inhibitor of aromatic L-amino acid decarboxylase (AADC).
PC-24805

Benserazide hydrochloride

AADC inhibitor,

Benserazide hydrochloride is a selective, peripherally acting aromatic L-amino acid decarboxylase (AADC) inhibitor, also is a potent inhibitor of bacterial T4P assembly ATPase PilB with IC50 of 3.68 uM.

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