Benzyl ((2S,3S)-3-methyl-1-(((S)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopentan-2-yl)carbamate;Z-ILE-LEU-ALDEHYDE;Z-IL-CHO;GAMMA-SECRETASE INHIBITOR XII;GSI-XII;γ-Secretase inhibitor XII;γ-Secretase inhibitor XII (GSI-XII)
Cas No.
161710-10-7
分子式
C20H30N2O4
分子量
362.46
包装储存
Powder
-20°C
3 years
4°C
2 years
In solvent
-80°C
6 months
-20°C
1 month
生物活性
Z-Ile-Leu-aldehyde (Z-IL-CHO) is a potent and competitive peptide aldehyde inhibitor of γ-secretase and notch.
性状
Solid
体外研究(In Vitro)
Z-Ile-Leu-aldehyde (ILCHO) significantly downregulates Th17-associated cytokine levels in murine Th17 体外研究 polarization assays.
Z-Ile-Leu-aldehyde (GSI XII) induces apoptosis of murine MOPC315.BM myeloma cells with high Notch activity.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
RT-PCRsup>[1]
Cell Line:
CD4 T cells from C57BL/6 mice.
Concentration:
25 μM.
Incubation Time:
24, 48, 72 hours.
Result:
DownregulateD ROR?t and IL-17 mRNA expression.
Cell Viability Assaysup>[2]
Cell Line:
MOPC315.BM cells.
Concentration:
0, 12, 15 μM.
Incubation Time:
24-48?h hours.
Result:
Reduced viability and induced apoptosis in MOPC315.BM cells
体内研究(In Vivo)
Z-Ile-Leu-aldehyde (GSI XII, 10?mg/kg, Intraperitoneally either for 14 days) controls myeloma bone disease mainly by targeting Notch in MM cells and possibly in osteoclasts in their microenvironment.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
MOPC315.BM mouse model.
Dosage:
10?mg/kg.
Administration:
Intraperitoneally either for 14 days.
Result:
Reduces myeloma-specific paraprotein levels in the MOPC315.BM model.
Diminished osteolytic lesions in the MOPC315.BM mice.