DAPT
description
Additional Information
Applications: | FA |
Synonyms: | gamma-Secretase Inhibitor IX, GSI IX, N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine tert-butyl ester |
Formulation: | Crystalline solid |
Chemical Name: | tert-butyl (2S)-2-[[(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoyl]amino]-2-phenylacetate |
Molecular Formula: | C23H26F2N2O4 |
Molecular Weight: | 432.5 |
CAS Number | 208255-80-5 |
Purity: | ≥95% |
Storage Conditions: | Product should be kept at -20°C. |
References: | 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. |