PD176252

≥99%

Reagent Code: #101882
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CAS Number 204067-01-6

science Other reagents with same CAS 204067-01-6

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Weight 584.67 g/mol
Formula C₃₂H₃₆N₆O₅
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

PD176252 is primarily used in research settings as a potent and selective inhibitor of the fibroblast growth factor receptor (FGFR) family. It is particularly valuable in studying the role of FGFR signaling pathways in various biological processes, including cell proliferation, differentiation, and survival. Researchers utilize PD176252 to investigate its potential therapeutic effects in diseases where FGFR signaling is dysregulated, such as certain cancers. By inhibiting FGFR activity, it helps in understanding the molecular mechanisms underlying tumor growth and progression, aiding in the development of targeted cancer therapies. Additionally, it is employed in preclinical studies to explore its efficacy in inhibiting angiogenesis, which is crucial for tumor development and metastasis.

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Size Availability Unit Price Quantity
inventory 2mg
10-20 days ฿14,364.00
inventory 5mg
10-20 days ฿28,728.00

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PD176252
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PD176252 is primarily used in research settings as a potent and selective inhibitor of the fibroblast growth factor receptor (FGFR) family. It is particularly valuable in studying the role of FGFR signaling pathways in various biological processes, including cell proliferation, differentiation, and survival. Researchers utilize PD176252 to investigate its potential therapeutic effects in diseases where FGFR signaling is dysregulated, such as certain cancers. By inhibiting FGFR activity, it helps in under

PD176252 is primarily used in research settings as a potent and selective inhibitor of the fibroblast growth factor receptor (FGFR) family. It is particularly valuable in studying the role of FGFR signaling pathways in various biological processes, including cell proliferation, differentiation, and survival. Researchers utilize PD176252 to investigate its potential therapeutic effects in diseases where FGFR signaling is dysregulated, such as certain cancers. By inhibiting FGFR activity, it helps in understanding the molecular mechanisms underlying tumor growth and progression, aiding in the development of targeted cancer therapies. Additionally, it is employed in preclinical studies to explore its efficacy in inhibiting angiogenesis, which is crucial for tumor development and metastasis.

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