475956
c-Myc抑制剂
≥95% (sum of two isomers, HPLC), c-Myc-Max interaction inhibitor, solid
别名:
c-Myc抑制剂, 10058-F4，（Z，E）-5-（4-乙基苄基）-2-硫代噻唑烷-4-酮
Product Name
c-Myc抑制剂, The c-Myc Inhibitor, also referenced under CAS 403811-55-2, controls the biological activity of c-Myc.
质量水平
方案
≥95% (sum of two isomers, HPLC)
表单
solid
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
protect from light
颜色
yellow
溶解性
DMSO: 200 mg/mL
运输
ambient
储存温度
2-8°C
SMILES字符串
S1\C(=C\c2ccc(cc2)CC)\C(=O)NC1=S
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 key
SVXDHPADAXBMFB-JXMROGBWSA-N
相关类别
一般描述
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
包装
用惰性气体包装
制备说明
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。
其他说明
Yin, X., et al. 2003.Oncogene22, 6151.
法律信息
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
免责声明
毒性：致癌/致畸（D）
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°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
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
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.
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