SNX-2112 (PF-04928473)
99%
Reagent
Code: #102548
CAS Number
908112-43-6
blur_circular Chemical Specifications
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Molecular Information
Weight
464.48 g/mol
Formula
C₂₃H₂₇F₃N₄O₃
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Registry Numbers
MDL Number
MFCD16038907
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Storage & Handling
Storage
-20℃
description Product Description
SNX-2112, also known as PF-04928473, is primarily investigated for its potential in cancer therapy. It functions as a heat shock protein 90 (HSP90) inhibitor, targeting the chaperone protein that plays a crucial role in stabilizing and activating numerous oncogenic client proteins. By inhibiting HSP90, SNX-2112 disrupts the stability and function of these client proteins, leading to the degradation of cancer-promoting molecules and ultimately inducing apoptosis in cancer cells. This mechanism makes it a promising candidate for treating various cancers, including those resistant to conventional therapies. Research has shown its efficacy in preclinical models of multiple myeloma, breast cancer, and other malignancies, highlighting its potential as a targeted therapeutic agent. Additionally, its ability to selectively target cancer cells while sparing normal cells reduces the risk of severe side effects, making it an attractive option for further clinical development.
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SNX-2112 (PF-04928473)
SNX-2112, also known as PF-04928473, is primarily investigated for its potential in cancer therapy. It functions as a heat shock protein 90 (HSP90) inhibitor, targeting the chaperone protein that plays a crucial role in stabilizing and activating numerous oncogenic client proteins. By inhibiting HSP90, SNX-2112 disrupts the stability and function of these client proteins, leading to the degradation of cancer-promoting molecules and ultimately inducing apoptosis in cancer cells. This mechanism makes it a promising candidate for treating various cancers, including those resistant to conventional therapies. Research has shown its efficacy in preclinical models of multiple myeloma, breast cancer, and other malignancies, highlighting its potential as a targeted therapeutic agent. Additionally, its ability to selectively target cancer cells while sparing normal cells reduces the risk of severe side effects, making it an attractive option for further clinical development.
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