Date published: 2025-10-17

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MerTK Inhibitors

MerTK inhibitors represent a specialized category of chemical compounds designed to specifically target and impede the activity of the MerTK receptor tyrosine kinase. MerTK, an abbreviation for Mer Tyrosine Kinase, is a prominent member of the TAM (Tyro3, Axl, and Mer) family of receptor kinases, which exert pivotal control over numerous cellular processes. Predominantly expressed on the surfaces of phagocytic cells, such as macrophages and dendritic cells, MerTK activation plays a central role in recognizing and engulfing apoptotic cells and cellular debris, a fundamental aspect of the body's immune response and tissue equilibrium. However, when MerTK becomes dysregulated or experiences overexpression, it has been linked to various diseases, including cancer, autoimmune disorders, and chronic inflammation.

Consequently, MerTK inhibitors have been meticulously engineered to selectively disrupt MerTK's signaling pathways. These inhibitors primarily function by binding to the catalytic site of MerTK, effectively obstructing the receptor's ability to phosphorylate downstream signaling molecules. Consequently, they interrupt its cellular functions, exerting influence over vital processes such as phagocytosis, cytokine production, and interactions between immune cells. The ramifications of MerTK inhibition extend to diseases characterized by irregular cell clearance, immune evasion, or tissue remodeling. Researchers are continually refining MerTK inhibitors, exploring their capacity to address health challenges associated with MerTK-related cellular pathways.

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Items 1 to 10 of 13 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Imatinib

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

Inhibits tyrosine kinases, particularly BCR-ABL and c-KIT, blocking cell signaling pathways in cancer cells.

Sorafenib

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

Targets RAF kinases and VEGFR, hindering cell proliferation and angiogenesis in cancer.

Gefitinib

184475-35-2sc-202166
sc-202166A
sc-202166B
sc-202166C
100 mg
250 mg
1 g
5 g
$62.00
$112.00
$214.00
$342.00
74
(2)

Inhibits epidermal growth factor receptor (EGFR), preventing cell growth and division in lung cancer.

MDV3100

915087-33-1sc-364354
sc-364354A
5 mg
50 mg
$240.00
$1030.00
7
(1)

Blocks the androgen receptor, impeding its activation in prostate cancer cells.

BMS 777607

1025720-94-8sc-364438
sc-364438A
10 mg
50 mg
$392.00
$1244.00
1
(1)

BMS-777607 is a multi-targeted tyrosine kinase inhibitor. Its mechanism involves binding to the ATP-binding sites of MET, AXL, Ron, and Tyro3 kinases, among which MerTK is inhibited. Its multi-target nature suggests a broader range of oncogenic pathways can be blocked.

Everolimus

159351-69-6sc-218452
sc-218452A
5 mg
50 mg
$128.00
$638.00
7
(1)

Inhibits mTOR, reducing cell growth and angiogenesis in various cancers.

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)

Targets EGFR, impeding cell growth in non-small cell lung cancer.

Ruxolitinib

941678-49-5sc-364729
sc-364729A
sc-364729A-CW
5 mg
25 mg
25 mg
$246.00
$490.00
$536.00
16
(1)

Inhibits JAK1 and JAK2, modulating cytokine signaling in myeloproliferative neoplasms.

Dasatinib

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

Blocks multiple tyrosine kinases, including BCR-ABL, inhibiting growth in chronic myeloid leukemia.

Lapatinib

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

Targets both EGFR and HER2, disrupting signaling pathways in breast cancer cells.