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首页-小分子抑制剂&激动剂-Others-Other Targets

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Cat. No. Product Name Information
PC-20717

RBP4 antagonist 59

RBP4 inhibitor

RBP4 antagonist 59 is a potent, selective and orally bioavailable retinol-binding protein 4 (RBP4) antagonist with HTRF IC50 of 16 nM.
PC-20703

IOI-42

hPEBP4 inhibitor

hPEBP4 inhibitor IOI-42 is a small molecule inhibitor of anti-apoptotic protein hPEBP4, potentiates TNF-α-mediated growth inhibition of MCF-7 breast cancer cells.
PC-20613

Perforin inhibitor 3

Perforin inhibitor

Perforin inhibitor 3 is a small molecule Perforin inhibitor, inhibits perforin-induced lysis of Jurkat T-lymphoma cells with IC50 of 0.78 uM.
PC-20612

Perforin inhibitor 2

Perforin inhibitor

Perforin inhibitor 2 is a small molecule Perforin inhibitor, inhibits perforin-induced lysis of Jurkat T-lymphoma cells with IC50 of 1.19 uM.
PC-20611

Perforin inhibitor 1

Perforin inhibitor

Perforin inhibitor 1 is a small molecule Perforin inhibitor, inhibits perforin-induced lysis of Jurkat T-lymphoma cells with IC50 of 2.3 uM.
PC-20610

Perforin inhibitor 5

Perforin inhibitor

Perforin inhibitor 5 is a small molecule Perforin inhibitor, inhibits perforin-induced lysis of Jurkat T-lymphoma cells with IC50 of 1.17 uM.
PC-20569

ERAD inhibitor CP26

Dislocation inhibitor

ERAD inhibitor CP26 (NSC26112) is a small molecule inhibitor of Hrd1 complex-mediated dislocation, inhibits NHK dislocation in HeLa cells with IC50 of 4.45 μM in the drGFP assays, shows broad-spectrum anti-flavivirus activity.
PC-49726

Seletracetam

SV2A ligand

Seletracetam (ucb 44212) is a high affinity for the synaptic vesicle protein 2A (SV2A) than levetiracetam with 10-fold, exhibits anticonvulsant properties in animal models of epilepsy.
PC-49471

MO-I-1100

ASPH inhibitor

MO-I-1100 is a small molecule inhibitor of aspartyl-(asparaginyl)-β-hydroxylase (ASPH), inhibits the β-hydroxylase activity of ASPH about 80%, inhibits Notch signaling in HCC cancer cells.
PC-49272

CRS0540

PolC inhibitor

CRS0540 is a potent, selective PolC DNA polymerase inhibitor that has demonstrated good in vitro and in vivo activity against Listeria monocytogenes.
PC-38598

Azo-resveratrol

Tyrosinase inhibitor

Azo-resveratrol is a potent mushroom tyrosinase inhibitor with IC50 of 36.28 uM.
PC-38531

ML266

GCase chaperone

ML266 (CID 46943215) is a non-inhibitory chaperone of glucocerebrosidase (GCase) enzyme, does not inhibit the enzyme’s action, but can facilitate its translocation to the lysosome.

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