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 About 34 results found for searched term "Phosphatase" (0.041 seconds)

Cat.No.  Name Target
M7528 Phosphatase Inhibitor Cocktail (EDTA-Free) Inhibitor Cocktails
AbMole Phosphatase Inhibitor Cocktail (EDTA-Free) is a mixture of phosphatase inhibitors prepared by 8 independent phosphatase inhibitors according to the optimized ratio. It is divided into A and B two tubes: A tube is a phosphate - root analogue to prevent the loss of phosphorylation of proteins and lipids, and B tube is a new natural product to provide more comprehensive protection for phosphorylation.
M9403 TPI-1 Phosphatase
Tyrosine Phosphatase Inhibitor 1
TPI-1 is a SHP-1 inhibitor, inhibits recombinant SHP-1 with an IC50 of 40 nM.
M9518 BN82002 Phosphatase
CDC25 Phosphatase Inhibitor I
BN82002, also known as CDC25 Phosphatase Inhibitor I, is a potent, selective, and irreversible inhibitor of CDC25 phosphatase family (IC50 = 2.4, 3.9, 6.3, 5.4, and 4.6 µM for 25A, 25B2, 25B3, 25C, and 25C-cat, respectively).
M11157 Alkaline phosphatase Metabolite/Endogenous Metabolite
Alkaline phosphatase is a membrane-binding glycoprotein that catalyzes the hydrolysis of monos phosphate esters at alkaline pH. Alkaline phosphatase can be used for molecular biology and enzyme-free analysis.
M1831 Cyclosporine A Immunology/Inflammation
Cyclosporine
Cyclosporin A is an immunosuppressant that binds to cyclophilin and inhibits calcineurin with an IC50 of 7 nM. cyclosporin A [CsA] binds to the cyclophilin 18 (Cyp18)-CsA complex. the Cyp18-CsA complex recruits calcium-regulated neurophosphatase (CaN), leading to the blocking of cytokine gene transcription in activated T cells. CsA is a highly specific inhibitor of T-cell activation.
M2849 Microcystin-LR Phosphatase
Cyanoginosin-LR; MC-LR; Toxin T 17 (Microcystis aeruginosa)
Microcystin-LR is a potent protein phosphatase inhibitor with IC50 of 0.04 nM for PP2A, >40-fold selectivity over PP1.
M2865 Sodium Monofluorophosphate Pyruvate Kinase
Monofluorophosphate is a competitive inhibitor of pyruvate kinase and alkaline phosphatase with Ki of 3.4 mM and 69 μM, respectively, which also irreversibly inhibits phosphorylase phosphatase with Ki of 0.5 mM.
M2922 Pentamidine dihydrochloride Parasite
MP601205 dihydrochloride
Pentamidine is an inhibitor of PRL Phosphatases and also inhibits synthesis of DNA, RNA and protein.
M2993 Sal003 Phosphatase
Sal003 is a potent and cell-permeable eIF-2α phosphatase inhibitor.
M3837 β-Glycerophosphate disodium salt hydrate Phosphatase
BGP; CAS# 154804-51-0
β-Glycerophosphate is a classical serine-threonine phosphatase inhibitor used in kinase reaction buffers.
M3943 Sanguinarine Apoptosis
Pseudochelerythrine; Sanguinarin
Sanguinarine, a plant alkaloid with anti-proliferative effects against cancers, is a potent and specific protein phosphatase (PP) 2C inhibitor.
M4562 Cantharidin Alkaloids
Cantharidin is a natural toxin inhibitor of protein phosphatases 1 and 2A (Ki values are 1.1 and 0.19 μM respectively). Displays > 500-fold selectivity over PP2B.
M4596 Silydianin Phosphatase
Silydianin, the active ingredient of silythistle, has anti-collagenase and anti-elastic enzyme activities. Silydianin is a natural protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 value of 17.38 μM. Silydianin inhibited the production and release of oxidation products in vitro.
M21540 L-Ascorbic Acid 2-phosphate (magnesium salt hydrate) Phosphatase
L-Ascorbic Acid 2-phosphate (magnesium salt hydrate) is a long-term vitamin C derivative that can stimulate the expression and formation of collagen. L-Ascorbic Acid 2-phosphate (magnesium salt hydrate) can be used as a medium to supplement osteogenic differentiation of human adipose stem cells (hASCs). Increased alkaline phosphatase (ALP) activity and runx2A expression in hASC during osteoblast differentiation.
M5102 PTP1B-IN-2 Phosphatase
PTP1B-IN-2 is a potent and selective protein tyrosine phosphatase-1B (PTP1B) inhibitor with IC50 of 50 nM.
M5161 Sodium orthovanadate ATPase
Sodium vanadate
Sodium orthovanadate is an alkaline phosphatase and (Na,K)-ATPase inhibitor with IC50 of 10 μM.
M5195 Okadaic acid Phosphatase
Okadaic acid is a potent inhibitor of protein phosphatase 1/2A with IC50 values of 19 nM and 0.2 nM for protein phosphatase 1 and protein phosphatase 2A, respectively.
M8990 LB-100 PPAR
CAS# 1632032-53-1
LB-100 is a water soluble protein phosphatase 2A (PP2A) inhibitor, with IC50 of 0.85 μM and 3.87 μM in BxPc-3 and Panc-1 cells.
M5348 (-)-Tetramisole Others
(-)-Tetramisole hydrochloride
(-)-Tetramisole is an inhibitor of alkaline phosphatase, used as an anthelmintic.
M5632 Etidronate Apoptosis
Etidronic acid
Etidronate is a class of non-aminobisphosphate that inhibits human protein tyrosine phosphatase activity and is used in the study of Paget's disease and in the prevention of ectopic ossification.
M5767 Menadione(Vitamin K3) DNA/RNA Synthesis
Menadione(Vitamin K3), a fat-soluble compound, is an inhibitor of Cdc25 phosphatase and mitochondrial DNA polymerase γ (pol γ), used as a nutritional supplement.
M5869 Pentamidine isethionate Parasite
Pentamidine diisethionate; Pentamidine isethionate salt
Pentamidine is an inhibitor of PRL Phosphatases and also inhibits synthesis of DNA, RNA and protein.
M5986 Suramin sodium salt P2 Receptor
Suramin hexasodium salt; BAY-205; NF-060
Suramin Sodium Salt (Suramin hexasodium salt) is a reversible inhibitor of competitive protein tyrosine phosphatases (PTPases).
M6293 Tacrolimus monohydrate Antibiotic
Fujimycin monohydrate; FR900506 monohydrate; FK506 monohydrate
Tacrolimus monohydrate binds to FK506 binding protein (FKBP). This complex inhibits calcineurin phosphatase (PP2B). Tacrolimus monohydrate is a mTOR-independent autophagy inducer.
M6300 (-)-p-Bromotetramisole Oxalate Phosphatase
L-p-Bromotetramisole Oxalate
(-)-p-Bromotetramisole Oxalate is a potent and non-specific alkaline phosphatase inhibitor.
M6383 A12B4C3 Others
A12B4C3 is a potent and selective polynucleotide kinase/phosphatase (PNKP) inhibitor.
M6542 BVT 948 Others
BVT 948 is a non-competitive protein tyrosine phosphatase inhibitor; enhances insulin signaling.
M6727 PFK-158 PFKFB3
ACT-PFK-158
PFK-158, also known as ACT-PFK-158, is a potent and selective inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatases (PFK-2/FBPase) isoform 3 (PFKFB3) with potential antineoplastic activity.
M6770 GSK 2830371 Phosphatase
GSK 2830371 is a potent and selective allosteric inhibitor of Wip1 phosphatase.
M6881 L-690,330 Phosphatase
L-690,330 is a inositol monophosphatase inhibitor.
M7057 NSC 663284 Others
DA-3003-1
NSC 663284 is a potent, selective Cdc25 phosphatase inhibitor.
M7059 NSC-87877 Phosphatase
NSC87877
Nsc-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatase with IC50 values of 0.318 μM and 0.355 μM, respectively. Nsc-87877 also inhibits bispecific phosphatase 26 (DUSP26).
M7060 NSC 95397 Phosphatase
NSC95397
NSC 95397 is a selective Cdc25 dual specificity phosphatase inhibitor.
M7246 Sanguinarine chloride Others
Pseudochelerythrine chloride; Sanguinarium chloride
Sanguinarine chloride is a inhibitor of protein phosphatase 2C (PP2C).



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