PF-06409577
10mM in DMSO
- Product Code: 224117
CAS:
1467057-23-3
| Molecular Weight: | 341.79 g./mol | Molecular Formula: | C₁₉H₁₆ClNO₃ |
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| EC Number: | MDL Number: | MFCD29917835 | |
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| Density: | Storage Condition: | -20°C |
Product Description:
PF-06409577 is primarily investigated for its potential therapeutic application in the treatment of diabetic nephropathy, a common complication of diabetes and a leading cause of chronic kidney disease. It functions as a selective activator of AMP-activated protein kinase (AMPK), a key enzyme involved in cellular energy homeostasis. Activation of AMPK in kidney cells helps reduce inflammation, oxidative stress, and fibrosis—key contributors to kidney damage in diabetes.
By targeting AMPK in the renal system, PF-06409577 has shown promise in preclinical studies to slow the progression of kidney injury without significantly affecting blood glucose levels, suggesting a direct renoprotective effect. This makes it a candidate for addressing organ-specific complications of diabetes beyond glycemic control. Its development highlights a targeted approach to treating metabolic stress in tissues highly susceptible to diabetic damage, particularly the kidneys.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1ml | 10-20 days | $276.17 |
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PF-06409577
PF-06409577 is primarily investigated for its potential therapeutic application in the treatment of diabetic nephropathy, a common complication of diabetes and a leading cause of chronic kidney disease. It functions as a selective activator of AMP-activated protein kinase (AMPK), a key enzyme involved in cellular energy homeostasis. Activation of AMPK in kidney cells helps reduce inflammation, oxidative stress, and fibrosis—key contributors to kidney damage in diabetes.
By targeting AMPK in the renal system, PF-06409577 has shown promise in preclinical studies to slow the progression of kidney injury without significantly affecting blood glucose levels, suggesting a direct renoprotective effect. This makes it a candidate for addressing organ-specific complications of diabetes beyond glycemic control. Its development highlights a targeted approach to treating metabolic stress in tissues highly susceptible to diabetic damage, particularly the kidneys.
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