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Z-Ile-Leu-aldehyde
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Z-Ile-Leu-aldehyde图片
CAS NO:161710-10-7
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
2mg电议
5mg电议
10mg电议
50mg电议
100mg电议

产品名称
Z-IL-CHO
GSI-XII
γ-Secretase inhibitor XII
产品介绍
Z-Ile-Leu-aldehyde (Z-IL-CHO) 是有效的、竞争性的γ-secretasenotch的肽醛抑制剂。
生物活性

Z-Ile-Leu-aldehyde (Z-IL-CHO) is a potent and competitive peptide aldehyde inhibitor ofγ-secretaseandnotch[1][2].

体外研究
(In Vitro)

Z-Ile-Leu-aldehyde (ILCHO) significantly downregulates Th17-associated cytokine levels in murine Th17 in vitro polarization assays[1].
Z-Ile-Leu-aldehyde (GSI XII) induces apoptosis of murine MOPC315.BM myeloma cells with high Notch activity[2].

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[2].

Animal Model:MOPC315.BM mouse model[2].
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.
分子量

362.46

性状

Solid

Formula

C20H30N2O4

CAS 号

161710-10-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 41 mg/mL(113.12 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.7589 mL13.7946 mL27.5893 mL
5 mM0.5518 mL2.7589 mL5.5179 mL
10 mM0.2759 mL1.3795 mL2.7589 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。