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Merck
CN
所有图片(2)

主要文件

352010

Sigma-Aldrich

谷氨酰胺酶抑制剂,化合物968

Glutaminase Inhibitor, Compd 968, is a cell-permeable, reversible inhibitor of mitochondrial glutaminase. Represses growth & invasive activity in glutaminase upregulated fibroblasts and tumor cells.

别名:

谷氨酰胺酶抑制剂,化合物968, GAC抑制剂、GLS1抑制剂I、KGA抑制剂I、肾型谷氨酰胺酶抑制剂I、5-(3-溴-4-(二甲氨基)苯基)-2,2-二甲基-2,3,5,6-四氢苯并[a]菲啶-4(1H)-酮

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About This Item

经验公式(希尔记法):
C27H27BrN2O
分子量:
475.42
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

方案

≥99% (HPLC)

表单

powder

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

white

溶解性

DMSO: 5 mg/mL

运输

ambient

储存温度

−20°C

SMILES字符串

O=C(CC(C)(C)C1)C2=C1C3=C(NC2C4=CC(Br)=C(C=C4)N(C)C)C=CC5=C3C=CC=C5

InChI key

NVFRRJQWRZFDLM-UHFFFAOYSA-N

一般描述

一种细胞可渗透的苯并菲啶酮化合物,可作为线粒体谷氨酰胺酶活性的变构和可逆抑制剂,并抑制谷氨酰胺酶上调的成纤维细胞和肿瘤细胞中的生长和侵袭活性(稳定表达Dbl,Cdc42-F28L,Rac-F28L或RhoC-F30L突变体以及SKBR3和MDA-MB231癌症细胞中的IC50 ≤ 10 µM)。在P-493B异种移植小鼠模型中显示可有效缩小肿瘤大小(200 µg/inj. i.p.,12天)。
一种细胞可渗透的苯并菲啶酮化合物,可作为线粒体谷氨酰胺酶活性的变构和可逆抑制剂,并抑制谷氨酰胺酶上调的成纤维细胞和肿瘤细胞中的生长和侵袭活性(稳定表达Dbl,Cdc42-F28L,Rac-F28L或RhoC-F30L突变体以及SKBR3和MDA-MB231癌症细胞中的IC50 ≤ 10 µM)。在P-493B异种移植小鼠模型中显示可有效缩小肿瘤大小(200 µg/inj. i.p.,12天)。也可以10 mM的DMSO溶液(货号506073)提供。

包装

用惰性气体包装

警告

毒性:标准处理(A)

其他说明

Wang, J.B., et al. 2010.Cancer Cell18, 207.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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