INCB054329

≥98%

Reagent Code: #100980
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CAS Number 1628607-64-6

science Other reagents with same CAS 1628607-64-6

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scatter_plot Molecular Information
Weight 348.36 g/mol
Formula C₁₉H₁₆N₄O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

INCB054329, also known as pemigatinib, is a selective inhibitor of Fibroblast Growth Factor Receptor (FGFR) kinases, primarily used in oncology for treating cancers associated with FGFR mutations or fusions. It is effective against various malignancies, such as urothelial carcinoma (bladder cancer), cholangiocarcinoma, lung cancer, and breast cancer. By blocking abnormal FGFR signaling pathways, it inhibits cancer cell proliferation and survival. This compound shows particular promise for patients with relapsed or refractory cancers resistant to other therapies. Its efficacy and safety are being evaluated in ongoing clinical trials, both as monotherapy and in combination with other anticancer agents, to target specific molecular pathways involved in tumor growth and progression.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿31,350.00
inventory 10mg
10-20 days ฿48,450.00

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INCB054329
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INCB054329, also known as pemigatinib, is a selective inhibitor of Fibroblast Growth Factor Receptor (FGFR) kinases, primarily used in oncology for treating cancers associated with FGFR mutations or fusions. It is effective against various malignancies, such as urothelial carcinoma (bladder cancer), cholangiocarcinoma, lung cancer, and breast cancer. By blocking abnormal FGFR signaling pathways, it inhibits cancer cell proliferation and survival. This compound shows particular promise for patients with r

INCB054329, also known as pemigatinib, is a selective inhibitor of Fibroblast Growth Factor Receptor (FGFR) kinases, primarily used in oncology for treating cancers associated with FGFR mutations or fusions. It is effective against various malignancies, such as urothelial carcinoma (bladder cancer), cholangiocarcinoma, lung cancer, and breast cancer. By blocking abnormal FGFR signaling pathways, it inhibits cancer cell proliferation and survival. This compound shows particular promise for patients with relapsed or refractory cancers resistant to other therapies. Its efficacy and safety are being evaluated in ongoing clinical trials, both as monotherapy and in combination with other anticancer agents, to target specific molecular pathways involved in tumor growth and progression.

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