Cell-permeable pyrrazolopyrimidine derivative that inhibits AMP kinase (Ki=109nM in the absence of AMP) in an ATP-competitive manner. It displays no significant inhibition of ZAPK, SYK, PKCT, PKA and JAK3. Decreases food intake in mice and inhibits the effects of AICAR and metformin. It has been shown to inhibit BMP type I receptors ALK2, ALK3 and ALK6. Promotes cardiomyogenesis in mouse embryonic stem cells. Induces protective autophagy in cancer cell lines.
Product Details
Alternative Name: | Compound C, Dorsomorphin |
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Formula: | C24H25N5O |
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MW: | 399.5 |
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CAS: | 866405-64-3 |
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Purity: | ≥98% (TLC) |
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Appearance: | Yellow solid. |
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Solubility: | Soluble in DMSO (3mg/ml, warm) |
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Shipping: | Blue Ice |
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Long Term Storage: | -20°C |
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Regulatory Status: | RUO - Research Use Only |
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Product Literature References
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SIRT1-Dependent Upregulation of BDNF in Human MicrogliaChallenged with Aβ: An Early but Transient Response Rescuedby Melatonin: G.I. Caruso, et al.; Biomedicines
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SIRT1 Mediates Melatonin's Effects on Microglial Activation in Hypoxia: In Vitro and In Vivo Evidence: S. Merlo, et al.; Biomolecules
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AMPK dependent protective effects of metformin on tumor necrosis factor-induced apoptotic liver injury: L. Cai, et al. ; Biochem. Biophys. Res. Commun.
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Abstract;
Compound C inhibits in vitro angiogenesis and ameliorates thrombin-induced endothelial barrier failure: D. Gündüz, et al.; Eur. J. Pharmacol.
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Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism: P. B. Yu et al.; Nat. Chem. Biol.
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C75, a fatty acid synthase inhibitor, reduces food intake via hypothalamic AMP-activated protein kinase: E. K. Kim et al.; J. Biol. Chem.
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