| 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. |
| M14493 | MSI-1436 lactate | MSI-1436 lactate is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTP1B), with an IC50 of 1 μM, 200-fold preference over TCPTP (IC50 of 224 μM). |
| M3837 | β-Glycerophosphate disodium salt hydrate | β-Glycerophosphate is a classical serine-threonine phosphatase inhibitor used in kinase reaction buffers. |
| M43526 | SHP2-IN-14 | SHP2-IN-14 is an orally active and potent SHP2 allosteric inhibitor (IC50=7 nM) with anti-tumor activity. |
| M43525 | SHP2-IN-13 | SHP2-IN-13 is a highly selective and orally active SHP2 “tunnel site” allosteric inhibitor with an IC50 of 83.0 nM. |
| M42553 | ITH12711 | ITH12711 is a PP2A ligand. |
| M42552 | Orellanine | Orellanine is a fungal nephrotoxin. |
| M42551 | Phosphatase-IN-1 | Phosphatase-IN-1 derivative, is a phosphatidate phosphatase (Pah) inhibitor. |
| M42550 | PTPN2/1-IN-2 | PTPN2/1-IN-2 is a PTPN2/1 antagonist that can be used in various tumor research. |
| M42549 | PTP1B/AKR1B1-IN-2 | PTP1B/AKR1B1-IN-2 is a dual PTP1B/AKR1B1 inhibitor (IC50s: 3.2 and 2.1 μM, Kis: 4.0 and 0.9μM). |
| M42548 | h-NTPDase8-IN-1 | h-NTPDase8-IN-1 is a sulfamoyl-benzamides based and selective inhibitor for h-NTPDases8 (IC50=0.28 μM). |
| M42547 | cis-Ferulic acid 4-O-β-D-glucopyranoside | cis-Ferulic acid 4-O-β-D-glucopyranoside is a phenolic glycosid, which can be isolated from Nitraria sibirica.. |
| M42546 | LYP-IN-4 | LYP-IN-4 is a reversible and selective inhibitor of lymphotyrosine phosphatase (LYP) (Ki=1.34 μM, IC50=3.52μM). |
| M42545 | h-NTPDase-IN-1 | h-NTPDase-IN-1 is a h-NTPDase inhibitor (IC50: 2.88 μM and 0.72 μM for h-NTPDase1 and h-NTPDase3 respectively). |
| M42544 | NC1 | NC1 is a noncompetitive and allosteric lymphoid-specific tyrosine phosphatase (LYP) inhibitor, with a Ki value 4.3 μM. |
| M42543 | PROTAC PTPN2 degrader-2 | PROTAC PTPN2 degrader-2 is a potent PTPN2 degrader with potential for studying cancer or metabolic diseases. |
| M42542 | PROTAC PTPN2 degrader-2 TFA | PROTAC PTPN2 degrader-2 TFA is a potent PTPN2 degrader with potential for studying cancer or metabolic diseases. |
| M42541 | Tegeprotafib | Tegeprotafib (PTPN2/1-IN-1) is an orally active PTPN1 and PTPN2 inhibitor with IC50s of 4.4 nM and 1-10 nM against PTPN2 and PTP1B, respectively. |
| M42540 | h-NTPDase-IN-5 | h-NTPDase-IN-5 is a pan-inhibitor of NTPDase with IC50s of 1.10 μM (h-NTPDase1), 44.73 μM (h-NTPDase2), 26.14 μM (h-NTPDase3), 0.32 μM (h- NTPDase8). |
| M42539 | h-NTPDase-IN-4 | h-NTPDase-IN-4 is a pan-inhibitor of NTPDase with IC50s of 3.58 μM (h-NTPDase1), 10.21 μM (h-NTPDase2), 0.13 μM (h-NTPDase3), 13.57 μM (h- NTPDase8). |
| M42538 | h-NTPDase-IN-3 | h-NTPDase-IN-3 is a pan-inhibitor of NTPDase with IC50s of 34.13 μM (h-NTPDase1), 0.33 μM (h-NTPDase2), 23.21 μM (h-NTPDase3), 2.48 μM (h- NTPDase8). |
| M42537 | LYP-IN-3 | LYP-IN-3 is a selective inhibitor of Lymphoid-tyrosine phosphatase (LYP) (Ki=0.93 μM), and regulates T-cell receptor (TCR) signaling pathway in tumor progress. |
| M42536 | PTP1B/AKR1B1-IN-1 | PTP1B/AKR1B1-IN-1 is a dual inhibitor of protein tyrosine phosphatase 1B (PTP1B) and aldose reductase (AKR1B1), with IC50s of 0.06 μM and 4.3 μM, respectively. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
