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Cat. No. Product Name Information
PC-22856

Thienopyridone

PRL/PTP4A inhibitor

Thienopyridone is a potent and selective phosphatase of regenerating liver (PRL) phosphatases inhibitor with IC50s of 173 nM, 277 nM and 128 nM for PRL-1 (PTP4A1), PRL-2 (PTP4A2), and PRL-3 (PTP4A3), respectively.
PC-22839

Cyclosporin A

PP2B inhibitor

Cyclosporin A (CsA, Cyclosporine A) is a immunosuppressant agent and highly specific inhibitor of the Ca2+/calmodulin-dependent protein phosphatase PP2B with IC50 of 65 nM in rat pancreatic acinar cells.
PC-22546

SMIP-031

PPM1A inhibitor

SMIP-031 is a potent small molecule inhibitor of metal-dependent phosphatase PPM1A with IC50 of 180 nM, efficiently activates autophagy and reduces the mycobacterium tuberculosis (Mtb) infection.
PC-22375

CDC14 phosphatase inhibitor 15

CDC14 inhibitor

CDC14 phosphatase inhibitor 15 is a first-in-class, potent, selective, and bioavailable inhibitor of CDC14 phosphatase with IC50 of 93 nM and 220 nM for human CDC14A and CDC14B, respectively, >50-fold selective over other PTPs.
PC-22168

SCP1 inhibitor GR-28

SCP1/REST inhibitor

SCP1 inhibitor GR-28 is a covalent small molecule inhibitor of small C-terminal domain phosphatase 1 (SCP1) with kinact/KI 1383 min-1 M-1, causes degrades REST protein in REST-dependent glioblastoma cells.
PC-21910

G6P3510

CLas STP inhibitor

G6P3510 is a specific Candidatus Liberibacter spp dual-specificity phosphatase (CLas STP) with binding KD of 81.4 uM, confers plant tolerance to Candidatus Liberibacter spp.
PC-21504

PRL inhibitor Cmpd-43

PRL inhibitor

PRL inhibitor Cmpd-43 is a specific small molecule inhibitor and detrimerizer of phosphatase of regenerating liver (PRL), significantly decreases PRL1 trimer formation inside the cell.
PC-21456

NGD61181

SHIP2 inhibitor

NGD61181 is a pyrazole-based SHIP2 inhibitor, has micromolar binding affinity and inhibitory activity, does not contain a phosphatase “warhead,” binds the active site of SHIP2.
PC-21455

SHIP1 inhibitor 23

SHIP1 inhibitor

SHIP1 inhibitor 23 is a small molecule SHIP1 inhibitor with IC50 of 6.5 uM in in the ratio pAKT/tAKT determined by Alpha SureFire assays.
PC-21454

AS1938909

SHIP2 inhibitor

AS1938909 is a potent, selective and competitive SHIP2 inhibitor with Ki value of 0.44 uM (human SHIP2), shows significant selectivity over other related phosphatases.
PC-21359

ATUX-792

PP2A activator

ATUX-792 is a small molecule activator of protein phosphatase 2A (PP2A), decreases survival, proliferation, and motility of neuroblastoma in vitro and tumor growth in vivo.
PC-21296

PP5 inhibitor P053

PP5 inhibitor

PP5 inhibitor P053 (Compound P053) is a potent, selective and competitive inhibitor of serine/threonine protein phosphatase-5 (PP5) with Ki of 244 nM, specifically binds and inhibits PP5 activity.

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