| T0745 | Disodium monofluorophosphate | Sodium Monofluorophosphate is a competitive inhibitor of pyruvate kinase and alkaline phosphatase, which also irreversibly inhibits phosphorylase phosphatase. |
| T0945 | Cyclosporin A | Cyclosporine A is a Calcineurin Inhibitor Immunosuppressant. The mechanism of action of cyclosporine is as a Calcineurin Inhibitor, and Cytochrome P450 3A4 Inhibitor, and P-Glycopr |
| T1927 | CCT007093 | CCT007093 is an effective PPM1D (WIP1) inhibitor (IC50: 8.4 μM). |
| T2189 | Sodium orthovanadate | Oxyvanadium ions in various states of oxidation. They act primarily as ion transport inhibitors due to their inhibition of Na(+)-, K(+)-, and Ca(+)-ATPase transport systems. They a |
| T2481 | Ascomycin | Ascomycin(Immunomycin, FR-900520, FK520) is an ethyl analog of tacrolimus (FK506) with strong immunosuppressant properties. |
| T3544 | SHP099 hydrochloride | SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor. |
| T4256 | PTP1B-IN-2 | PTP1B-IN-2 is an effective protein tyrosine phosphatase 1B (PTP1B) inhibitor(IC50=50 nM). |
| T4308 | F1063-0967 | F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 of 11.62 μM. |
| T4340 | SPI 112 | SPI-112, the SPI-112 methyl ester analog, can inhibit cellular Shp2 PTP activity. SPI-112 bound to Shp2 by surface plasmon resonance (SPR) and displayed competitive inhibitor kinet |
| T4491 | LMPTP INHIBITOR 1 hydrochloride (1908414-82-3(free base)) | LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. |
| T4671 | CDC25 Phosphatase Inhibitor I | BN82002 is a synthetic inhibitor of CDC25 phophatases |
| T6459 | Cyclosporine | Cyclosporine is a calcineurin phosphatase pathway inhibitor, used as an immunosuppressant drug to prevent rejection in organ transplantation. |
| T6521 | GSK2830371 | GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM. |
| T7084 | PTP Inhibitor I | PTP Inhibitor I is a cell-permeable, protein tyrosine phosphatase (PTP) inhibitor that covalently blocks the catalytic domain of the Src homology region 2 domain-containing phospha |
