| Cat.No. | Name | Information |
|---|---|---|
| M2849 | Microcystin-LR | Microcystin-LR is a potent protein phosphatase inhibitor with IC50 of 0.04 nM for PP2A, >40-fold selectivity over PP1. |
| M6314 | SHP099 | SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor with IC50 =0.07 μM and p-ERK modulation in cells IC50 = 0.250 μM. |
| M7533 | SHP099 hydrochloride | SHP099 hydrochloride is a potent, selective, orally available SHP2 inhibitor with an IC50 of 70 nM. |
| M57213 | LYP-IN-1 | LYP-IN-1 is a potent, selective and specific LYP inhibitor with a Ki and an IC50 of 110 nM and 0.259 μM, respectively. |
| M57212 | PF-07284892 | PF-07284892 (ARRY-558) is a potent and orally active SHP2 inhibitor with an IC50 value of 21 nM. |
| M56750 | MY10 | MY10 is a potent and orally active receptor protein tyrosine phosphatase (RPTPβ/ζ) inhibitor. |
| M56749 | CPDA | CPDA is a novel potent SH2 domain-containing inositol phosphatase 2 (SHIP2) inhibitor. |
| M56748 | HKB99 | HKB99 is an allosteric inhibitor of phosphoglycerate mutase 1 (PGAM1). |
| M56747 | 7-BIA | 7-BIA is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with an IC50 of ~1-3 μM. |
| M56746 | MY33-3 | MY33-3 is a potent and selective inhibitor of receptor protein tyrosine phosphatase (RPTP)β/ζ, with an IC50 of ~0.1 μM. |
| M56745 | CX08005 | CX08005 is a competitive PTP1B inhibitor. |
| M56744 | ARL67156 | ARL67156 is an inhibitor of ecto-ATPase. |
| M56743 | PTP1B-IN-3 | PTP1B-IN-3 is a potent and orally active PTP1B inhibitor with IC50s of 120 nM for both PTP1B and TCPTP. |
| M56742 | PPM1A-IN-1 | PPM1A-IN-1 is an inhibitor for PP2C Ser/Thr phosphatase protein phosphatase Mg2+/Mn2+-dependent 1A. |
| M56741 | (Rac)-RK-682 | (Rac)-RK-682, a racemate of RK-682, is a protein tyrosine phosphatases (PTPases) inhibitor. |
| M56740 | PTP1B-IN-15 | PTP1B-IN-15 is a potent and selective inhibitor of protein tyrosine phosphatase 1B (PTP1B). |
| M56739 | 5-FAM-Alkyne | 5-FAM-Alkyne is a high selective and sensitive fluorescent biosensor for alkaline phosphatase (ALP). |
| M56738 | Naphthol AS-BR | Naphthol AS-BR is a substrate for the histochemical demonstration of acid and alkaline phosphatase. |
| M56737 | PTP Inhibitor IV | PTP Inhibitor IV is a protein tyrosine phosphatase (PTP) inhibitor that competitively inhibits DUSP14 phosphatase activity with an 50 of 5.21 μM. |
| M56736 | MY33-3 hydrochloride | MY33-3 hydrochloride is a potent and selective inhibitor of receptor protein tyrosine phosphatase (RPTP)β/ζ, with an IC50 of ~0.1 μM. |
| M56735 | (R)-Azasetron besylate | (R)-Azasetron besylate (SENS-401) is an orally active calcineurin inhibitor. |
| M56734 | PTP1B-IN-3 diammonium | PTP1B-IN-3 diammonium is a potent and orally active PTP1B inhibitor with IC50s of 120 nM for both PTP1B and TCPTP. |
| M56733 | Icerguastat Carbonate | Icerguastat (Sephin1) Carbonate, a derivative of Guanabenz lacking the α2-adrenergic activity, is a selective inhibitor of the phosphatase regulatory subunit PPP1R15A (R15A). |
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