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Cat. No. Product Name Information
PC-70158

DT-061

PP2A activator

SMAP (DT-061, NZ-8-061) is an orally bioavailable small molecule activator of PP2A, inhibits KRAS-driven tumor growth.
PC-70157

CS-11

PP2A-β-catenin inhibitor

CS-11 is a novel small molecule inhibitor that inhibits PP2A and β-catenin interaction by selectively engaging PR55α binding site (Kd=45 pM).
PC-70156

MP07-66

PP2A activator

MP07-66 is a novel FTY720 analog that acts as PP2A activator, disrupts the SET/PP2A interaction devoid of immunosuppressive effects leads to the reactivation of PP2A.
PC-70155

LB102

PP2A inhibitor

LB102 (LB-1.2, LB 102) is a potent, selective serine/threonine protein phosphatase 2A (PP2A) inhibitor with IC50 of 0.4 uM.
PC-70136

AS1949490

SHIP2 inhibitor

AS-1949490 (AS1949490) is a potent, selective SHIP2 inhibitor with IC50 of 0.34/0.62 uM for mouse/human SHIP2.
PC-60249

BN82002

CDC25 phosphatase inhibitor

BN82002 is a potent Cdc25 dual specificity phosphatase inhibitor with IC50 of 2-6 uM for Cdc25A/B/C.
PC-60248

NSC95397

Cdc25 inhibitor

NSC95397 is a potent, selective, reversible Cdc25 dual specificity phosphatase inhibitor with Ki of 32/96/40 nM for Cdc25A/B/C, respectively.
PC-60183

DUSP6 inhibitor BCI

DUSP6 inhibitor

BCI (NSC150117) is a small-molecule, allosteric inhibitor of DUSP6 (dual-specificity phosphatase 6) with IC50 of 12.3 uM.
PC-60081

Razuprotafib sodium

VE-PTP inhibitor

AKB-9778 (Razuprotafib) sodium is a potent, selective inhibitor of vascular endothelial protein tyrosine phosphatase (VE-PTP, HPTPβ) with IC50 of 17 pM.
PC-45587

Calyculin A

Phosphatase inhibitor

Calyculin A is a more potent phosphatase inhibitor than Okadaic acid, inhibits catalytic subunit of type-2A phosphatase (IC50 =0.5-1 nM), calyculin A is more effective for protein phosphatase type-1.
PC-42921

MSI-1436

PTP1B inhibitor

MSI-1436 (Trodusquemine) is an non-competitive, allosteric inhibitor of PTP1B with Ki of 0.6 uM for PTP1B 1-405.
PC-42129

SHP-099 hydrochloride

SHP2 inhibitor

SHP-099 hydrochloride is a potent, selective, allosteric and orally bioavailable protein tyrosine phosphatase SHP2 inhibitor with IC50 of 71 nM.

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