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Cat. No. Product Name Information
PC-24577

MBLAC2 inhibitor KV-79

MBLAC2 inhibitor

MBLAC2 inhibitor KV-79 is a potent, specific inhibitor of the metalloenzyme MBLAC2 (Metallo-Beta-Lactamase Domain Containing 2) with EC50 of 24 nM, >60 fold selectivity over HDAC6.
PC-24576

MBLAC2 inhibitor KV-65

MBLAC2 inhibitor

MBLAC2 inhibitor KV-65 is a potent, specific inhibitor of the metalloenzyme MBLAC2 (Metallo-Beta-Lactamase Domain Containing 2) with EC50 of 37 nM, 64-fold selectivity over HDAC6.
PC-24553

FGH10019

SREBP inhibitor

FGH10019 is a specific small molecule inhibitor of sterol regulatory element-binding protein (SREBP) with IC50 of 0.7 uM in SREBP-responsive reporter gene assays.
PC-24547

Fascin inhibitor G2

Fascin inhibitor

Fascin inhibitor G2 is a small molecule inhibitor of Fascin (FSCN1), inhibits the actin-bundling function of fascin with IC50 of 5-8 uM, blocks tumour invasion and metastatic colonization.
PC-24546

NP-G2-029

Fascin inhibitor

Fascin inhibitor G2 (NP-G2-029) is a specific small molecule inhibitor of Fascin (FSCN1) with IC50 of 0.19 uM in F-actin-bundling assay.
PC-24544

Z1362873773

Fascin inhibitor

Z1362873773 is a novel small molecule inhibitor of Fascin (FSCN1), reduces the fascin bundling activity.
PC-24532

DDL-357

Secreted clusterin enhancer

DDL-357 is a small molecule secreted isoform of clusterin (sCLU) enhancer with EC50 of 223 nM, increases brain sCLU in the murine ApoE4TR-5XFAD model of AD.
PC-24529

NUV-244

PNPLA3 I148M degrader

NUV-244 is a potent, specific small molecule degrader of PNPLA3 I148M variant, degrades PNPLA3 I148M via the ubiquitin-proteasome system and involving the E3 ligase BFAR.
PC-24520

GI-Y2

GSDMD inhibitor

GI-Y2 (GSDMD inhibitor Y2) is a specific small molecule inhibitor of Gasdermin D (GSDMD), directly interacts with the Arg10 residue of GSDMD (SPR KD=36.0 uM) and reduces the membrane binding of N‐terminal domain (GSDMD‐N).
PC-24478

CLEC-2 inhibitor MAS9

CLEC-2 inhibitor

MAS9 is a specific small molecule inhibitor targeting the C-type lectin-like receptor-2 (CLEC-2)-podoplanin interaction with IC50 of 4.5 uM, inhibits CLEC-2-mediated platelet aggregation.
PC-24463

FICD inhibitor C22

FICD inhibitor

FICD inhibitor C22 is a specific, cell-permeable inhihitor of the AMP transferase FICD, significantly inhibits endogenous FICD-mediated BiP AMPylation (IC50=7.27 uM) while weakly inhibiting BiP deAMPylation.
PC-24451

Mitochondrial complex I inhibitor C458

CAS 2001090-87-3

C458 is nontoxic mitochondrial complex I (mtCI) inhibitor with highly protective against Aβ toxicity, C458 protects MC65 Tet-Off cells (Aβ expressed) with an EC50 of 4.6 nM.

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