PTPRQ inhibitors represent a diverse class of chemical compounds designed to modulate the activity of the protein tyrosine phosphatase receptor type Q (PTPRQ). PTPRQ is a transmembrane receptor protein that plays a pivotal role in regulating various cellular processes through its phosphatase activity, particularly in signal transduction pathways. Inhibitors of PTPRQ are developed to manipulate this enzyme's activity and investigate its involvement in cellular functions. These inhibitors often exhibit specific mechanisms of action that target the catalytic site of PTPRQ, preventing its dephosphorylation of tyrosine residues on target substrates.
The chemical class of PTPRQ inhibitors comprises a range of small molecules, each with unique chemical structures and modes of action. These inhibitors are designed to interact with the active site of PTPRQ, thereby impeding its catalytic function. Typically, they include compounds that mimic the structure of the substrate, enabling them to competitively bind to the enzyme's active site and interfere with its ability to dephosphorylate tyrosine residues on target proteins. PTPRQ inhibitors are essential research tools for elucidating the roles of PTPRQ in various cellular processes, including signal transduction, cell adhesion, and cellular growth. By selectively inhibiting PTPRQ, researchers can gain insights into the intricate network of signaling pathways regulated by this phosphatase and its implications in cellular physiology and pathology.In summary, PTPRQ inhibitors constitute a class of chemical compounds designed to interfere with the catalytic activity of the protein tyrosine phosphatase receptor type Q. These inhibitors vary in structure and mechanism of action but are primarily developed as valuable tools for studying the functions of PTPRQ in cellular processes.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib inhibits PTPRQ by binding to its active site, blocking its phosphatase activity. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib hinders PTPRQ activity by disrupting its signaling pathways, especially in cancer cells. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib targets PTPRQ in cells by blocking its enzymatic activity. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
Sunitinib inhibits PTPRQ in cells by interfering with its downstream signaling pathways, reducing tumor growth and angiogenesis. | ||||||
Lapatinib | 231277-92-2 | sc-353658 | 100 mg | $412.00 | 32 | |
Lapatinib targets PTPRQ in cells by blocking its phosphorylation, inhibiting cancer cell proliferation. | ||||||
Nilotinib | 641571-10-0 | sc-202245 sc-202245A | 10 mg 25 mg | $205.00 $405.00 | 9 | |
Nilotinib inhibits PTPRQ in cells by binding to its active site, suppressing its phosphatase activity, and reducing cell proliferation. | ||||||
Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
Vandetanib inhibits PTPRQ in cells by blocking its signaling pathways, thereby hindering tumor growth and angiogenesis. | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $85.00 $132.00 $287.00 $495.00 $3752.00 | 42 | |
Erlotinib targets PTPRQ in cells by inhibiting its phosphorylation, leading to reduced cell proliferation. | ||||||
Regorafenib | 755037-03-7 | sc-477163 sc-477163A | 25 mg 50 mg | $320.00 $430.00 | 3 | |
Regorafenib inhibits PTPRQ in cells by disrupting its downstream signaling pathways, reducing tumor growth. | ||||||
AP 24534 | 943319-70-8 | sc-362710 sc-362710A | 10 mg 50 mg | $172.00 $964.00 | 2 | |
AP 24534 targets PTPRQ in cells by inhibiting its enzymatic activity, leading to reduced cell proliferation. |