Txk inhibitors belong to a distinctive class of chemical compounds designed to target and modulate the activity of the tyrosine kinase expressed in T cells, known as Txk. Tyrosine kinases are pivotal components in cellular signaling pathways, orchestrating the transfer of phosphate groups to tyrosine residues within proteins. Txk, a member of the Tec family of tyrosine kinases, plays a crucial role in the regulation of immune responses, particularly in T lymphocytes. These inhibitors are meticulously crafted to interact selectively with Txk, disrupting its catalytic function and impeding downstream signaling cascades.
The design of Txk inhibitors is rooted in an in-depth understanding of the molecular structure and function of the target kinase. By exploiting the unique structural features of Txk, researchers have developed small molecules that can specifically bind to the kinase's active site, hindering its ability to phosphorylate substrate proteins. The selectivity of Txk inhibitors is a critical aspect of their design, as it allows for precise modulation of immune responses without affecting other essential kinases. This targeted approach is paramount in ensuring the efficacy of the inhibitors while minimizing potential off-target effects.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib is a broad-spectrum tyrosine kinase inhibitor that can inhibit Src family kinases, which may affect Txk activity. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib targets BCR-ABL and c-Kit, which are related to tyrosine kinase signaling and can influence Txk's pathway. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
Sunitinib inhibits receptor tyrosine kinases such as VEGFR, PDGFR, and can alter signaling pathways that interact with Txk. | ||||||
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 selectively inhibits EGFR tyrosine kinase, which can modulate downstream effects on Txk-related pathways. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib targets multiple receptor tyrosine kinases (RTKs) involved in the MAPK pathway, potentially affecting Txk signaling. | ||||||
Lapatinib | 231277-92-2 | sc-353658 | 100 mg | $412.00 | 32 | |
Lapatinib is a dual inhibitor of EGFR and HER2, which may indirectly inhibit Txk through downstream signaling disruption. | ||||||
Pazopanib | 444731-52-6 | sc-396318 sc-396318A | 25 mg 50 mg | $127.00 $178.00 | 2 | |
Pazopanib inhibits VEGFR, PDGFR, and c-Kit, possibly altering Txk-related angiogenesis and cell proliferation signals. | ||||||
Nilotinib | 641571-10-0 | sc-202245 sc-202245A | 10 mg 25 mg | $205.00 $405.00 | 9 | |
Nilotinib is a selective BCR-ABL inhibitor that could impact signaling pathways linked to Txk function. | ||||||
Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
Vandetanib inhibits VEGFR and EGFR, which may perturb signaling networks that include Txk. | ||||||
AP 24534 | 943319-70-8 | sc-362710 sc-362710A | 10 mg 50 mg | $172.00 $964.00 | 2 | |
Ponatinib is a multi-targeted tyrosine kinase inhibitor, which may also affect Txk through broad-spectrum kinase inhibition. | ||||||