NL-1

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Chemical Structure| 188532-26-5 同义名 : -
CAS号 : 188532-26-5
货号 : A1226353
分子式 : C18H25NO3S
纯度 : 98%
分子量 : 335.461
MDL号 : MFCD32671359
存储条件:

Pure form Sealed in dry,Store in freezer, under -20°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 250 mg/mL(745.24 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 MitoNEET (CISD1) is a mitochondrial outer membrane protein that plays a critical role in maintaining mitochondrial homeostasis and is frequently overexpressed in cancer. NL-1, derived from pioglitazone, is a mitoNEET inhibitor with antileukemic activity. Treatment with NL-1 reduced the number of viable cells in both REH and REH/Ara-C cell lines in a concentration-dependent manner. The IC50 value of NL-1 was comparable in REH (47.35 ± 7.7 μM) and REH/Ara-C (56.26 ± 8.8 μM) cells. Furthermore, the NL-1 treatment (60 μM; 72 hours) consistently reduced the size and number of preformed SD1 spheroids in SD1 ALL cells. Additionally, both the number of live cells and the percentage of viability of the cells was reduced when treated with NL-1. NL-1 pretreatment inhibited the chemotactic ability of both REH and REH/Ara-C cells to migrate toward multiple chemoattractants. The cells treated with NL-1 showed a dose-dependent decrease in chemotaxis in both cells. Treatment of BMSC and HOB cocultures with NL-1 (60 μM) decreased the number of live cells recovered from the S and PD cell populations and decreased viability of the PD population. Further, treatment with NL-1 (60 μM; 6 hours) increased the fluorescence intensity compared with untreated cells, indicating an increase in autophagy. In mice, the NL-1–treated group (1 mg/kg per day) showed significantly lower tumor burden than the control vehicle–treated group on day 14 postinjection[1].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.98mL

0.60mL

0.30mL

14.90mL

2.98mL

1.49mL

29.81mL

5.96mL

2.98mL

参考文献

[1]Geldenhuys WJ, Nair RR, Piktel D, Martin KH, Gibson LF. The MitoNEET Ligand NL-1 Mediates Antileukemic Activity in Drug-Resistant B-Cell Acute Lymphoblastic Leukemia. J Pharmacol Exp Ther. 2019;370(1):25-34