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品質等級
化驗
≥95% (sum of two isomers, HPLC)
形狀
solid
製造商／商標名
Calbiochem®
儲存條件
OK to freeze
protect from light
顏色
yellow
溶解度
DMSO: 200 mg/mL
運輸包裝
ambient
儲存溫度
2-8°C
InChI
1S/C12H11NOS2/c1-2-8-3-5-9(6-4-8)7-10-11(14)13-12(15)16-10/h3-7H,2H2,1H3,(H,13,14,15)/b10-7+
InChI 密鑰
SVXDHPADAXBMFB-JXMROGBWSA-N
一般說明
一种可渗透细胞的噻唑烷酮化合物，可特异性抑制c-Myc-Max相互作用，从而阻止c-Myc靶向基因表达的反式激活。显示在体外和体内均以c-Myc依赖性方式抑制肿瘤细胞生长（64 μM，使用c-Myc转染的大鼠1a成纤维细胞）。
一种可渗透细胞的噻唑烷酮化合物，可特异性抑制c-Myc-Max相互作用，从而阻止c-Myc靶向基因表达的反式激活。显示在体外和体内均以c-Myc依赖性方式抑制肿瘤细胞生长（有效浓度：64 µM，使用c-Myc转染的大鼠1a成纤维细胞）。
生化／生理作用
主要靶标
c-Myc
c-Myc
产物不与ATP竞争。
可逆：否
细胞可渗透性：具有
包裝
用惰性气体包装
警告
毒性：致癌/致畸（D）
重構
复溶后，等分并冷冻保存（-20°C）。贮备液在-20°C下可稳定保存至多3个月。
其他說明
Yin, X., et al. 2003.Oncogene22, 6151.
法律資訊
根据美国专利号7,026,343的许可证销售。
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Sens. 1
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
Andrea Arena et al.
Biomedicines, 10(4) (2022-04-24)
Multiple myeloma (MM) and primary effusion lymphoma (PEL) are aggressive hematological cancers, for which the search for new and more effective therapies is needed. Both cancers overexpress c-Myc and are highly dependent on this proto-oncogene for their survival. Although c-Myc
Roberta Gonnella et al.
Cancers, 15(23) (2023-12-09)
Heat shock proteins (HSPs) are highly expressed in cancer cells and represent a promising target in anti-cancer therapy. In this study, we investigated for the first time the expression of high-molecular-weight HSP110, belonging to the HSP70 family of proteins, in
Le Tran Phuc Khoa et al.
Nature communications, 15(1), 1721-1721 (2024-02-27)
Quiescence in stem cells is traditionally considered as a state of inactive dormancy or with poised potential. Naive mouse embryonic stem cells (ESCs) can enter quiescence spontaneously or upon inhibition of MYC or fatty acid oxidation, mimicking embryonic diapause in vivo.
Wei Fan et al.
eLife, 10 (2021-05-28)
Sphingolipids are important structural components of cell membranes and prominent signaling molecules controlling cell growth, differentiation, and apoptosis. Sphingolipids are particularly abundant in the brain, and defects in sphingolipid degradation are associated with several human neurodegenerative diseases. However, molecular mechanisms
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