DAPT
description
Additional Information
Applications:
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FA
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Synonyms:
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gamma-Secretase Inhibitor IX, GSI IX, N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine tert-butyl ester
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Formulation:
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Crystalline solid
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Chemical Name:
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tert-butyl (2S)-2-[[(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoyl]amino]-2-phenylacetate
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Molecular Formula:
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C23H26F2N2O4 |
Molecular Weight: |
432.5
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CAS Number
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208255-80-5
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Purity:
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≥95%
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Storage Conditions:
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Product should be kept at -20°C.
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References:
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El Mouedden, M., Vandermeeren, M., Meert, T., & Mercken, M. (2005). Reduction of Abeta levels in the Sprague Dawley rat after oral administration of the functional gamma-secretase inhibitor, DAPT: a novel non-transgenic model for Abeta production inhibitors. Current pharmaceutical design, 12(6), 671-676. Yagishita, S., Morishima-Kawashima, M., Tanimura, Y., Ishiura, S., & Ihara, Y. (2006). DAPT-induced intracellular accumulations of longer amyloid β-proteins: further implications for the mechanism of intramembrane cleavage by γ-secretase. Biochemistry, 45(12), 3952-3960. Crawford, T. Q., & Roelink, H. (2007). The Notch response inhibitor DAPT enhances neuronal differentiation in embryonic stem cell‐derived embryoid bodies independently of sonic hedgehog signaling. Developmental Dynamics,236(3), 886-892. Grottkau, B. E., Friedrich, C. C., Jing, W., & Wu, Y. (2009). DAPT enhances the apoptosis of human tongue carcinoma cells. International journal of oral science, 1(2), 81-89. |