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Merck
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Key Documents

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號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

品質等級

化驗

≥99% (HPLC)

形狀

powder

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

white

溶解度

DMSO: 5 mg/mL

運輸包裝

ambient

儲存溫度

−20°C

SMILES 字串

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

一般說明

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。

包裝

用惰性气体包装

警告

毒性:标准处理(A)

其他說明

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

法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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