Date published: 2025-10-26

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Txk Inhibitors

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.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$47.00
$145.00
51
(1)

Dasatinib is a broad-spectrum tyrosine kinase inhibitor that can inhibit Src family kinases, which may affect Txk activity.

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$25.00
$117.00
$209.00
27
(1)

Imatinib targets BCR-ABL and c-Kit, which are related to tyrosine kinase signaling and can influence Txk's pathway.

Sunitinib, Free Base

557795-19-4sc-396319
sc-396319A
500 mg
5 g
$150.00
$920.00
5
(0)

Sunitinib inhibits receptor tyrosine kinases such as VEGFR, PDGFR, and can alter signaling pathways that interact with Txk.

Erlotinib, Free Base

183321-74-6sc-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
(0)

Erlotinib selectively inhibits EGFR tyrosine kinase, which can modulate downstream effects on Txk-related pathways.

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

Sorafenib targets multiple receptor tyrosine kinases (RTKs) involved in the MAPK pathway, potentially affecting Txk signaling.

Lapatinib

231277-92-2sc-353658
100 mg
$412.00
32
(1)

Lapatinib is a dual inhibitor of EGFR and HER2, which may indirectly inhibit Txk through downstream signaling disruption.

Pazopanib

444731-52-6sc-396318
sc-396318A
25 mg
50 mg
$127.00
$178.00
2
(1)

Pazopanib inhibits VEGFR, PDGFR, and c-Kit, possibly altering Txk-related angiogenesis and cell proliferation signals.

Nilotinib

641571-10-0sc-202245
sc-202245A
10 mg
25 mg
$205.00
$405.00
9
(1)

Nilotinib is a selective BCR-ABL inhibitor that could impact signaling pathways linked to Txk function.

Vandetanib

443913-73-3sc-220364
sc-220364A
5 mg
50 mg
$167.00
$1353.00
(1)

Vandetanib inhibits VEGFR and EGFR, which may perturb signaling networks that include Txk.

AP 24534

943319-70-8sc-362710
sc-362710A
10 mg
50 mg
$172.00
$964.00
2
(1)

Ponatinib is a multi-targeted tyrosine kinase inhibitor, which may also affect Txk through broad-spectrum kinase inhibition.