Ambeed.cn

首页 / 抑制剂/激动剂 / 细胞凋亡 / / 10074-G5

10074-G5 {[allProObj[0].p_purity_real_show]}

货号:A188479

10074-G5 is a c-Myc Max interaction inhibitor.

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
10074-G5 化学结构 CAS号:413611-93-5
10074-G5 化学结构
CAS号:413611-93-5
10074-G5 3D分子结构
CAS号:413611-93-5
10074-G5 化学结构 CAS号:413611-93-5
10074-G5 3D分子结构 CAS号:413611-93-5
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price) ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price) ]}
{[ getRatePrice(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} 现货 1周 咨询 - +
购物车0 收藏 询单

10074-G5 纯度/质量文件 产品仅供科研

货号:A188479 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

全球学术期刊中引用的产品

更多 >

10074-G5 生物活性

描述 10074-G5 is effective in hindering the proliferation of Daudi Burkitt's lymphoma cells and in interfering with the dimerization of c-Myc/Max. It exhibits IC50 values of 15.6 μM for Daudi cells and 13.5 μM for HL-60 cells[1]. 10074-G5 interacts with the Myc peptide Myc353-437, exhibiting a Kd value of 2.8 μM within the Arg363-Ile381 region. It attaches within a pocket formed by a bend (Asp379-Ile381) at the N-terminal end of an induced helical segment (Leu370–Arg378)[2].
作用机制 10074-G5 can disrupt the dimeric complex formed between its basic helix-loop-helix leucine zipper (bHLHZip) domain and a similar domain on its dimerization partner, Max. Similar to 10058-F4, 10074-G5 binds to c-Myc, but a distinct region[1]. [1] [2] [3] [4] [5]

10074-G5 细胞研究

细胞系 浓度 检测类型 检测时间 活性说明 数据源
Daudi cells Cytotoxicity assay 3 to 5 days Cytotoxicity against human Daudi cells assessed as growth inhibition after 3 to 5 days by MTT assay, IC50=10 Μm 23177256
HL60 cells Cytotoxicity assay 3 to 5 days Cytotoxicity against human HL60 cells assessed as growth inhibition after 3 to 5 days by MTT assay, IC50=30 μM 23177256

10074-G5 动物研究

Dose Mice[4] (i.v.): 20 mg/kg
Administration i.v.
Pharmacokinetics
Animal Mice[4]
Dose 20 mg/kg
Administration i.v.
Cmax 58.5 ± 2.7 nmol/ml
T1/2 37 min
CL 69 ml/min/kg
Vd 3000 ml/kg

10074-G5 参考文献

[1]Hammoudeh DI, Follis AV, et al. Multiple independent binding sites for small-molecule inhibitors on the oncoprotein c-Myc. J Am Chem Soc. 2009 Jun 3;131(21):7390-401.

[2]Yap JL, Wang H, et al. Pharmacophore identification of c-Myc inhibitor 10074-G5. Bioorg Med Chem Lett. 2013 Jan 1;23(1):370-4.

[3]Yin X, Giap C, et al. Low molecular weight inhibitors of Myc-Max interaction and function. Oncogene. 2003 Sep 18;22(40):6151-9.

[4]Clausen DM, Guo J, et al. In vitro cytotoxicity and in vivo efficacy, pharmacokinetics, and metabolism of 10074-G5, a novel small-molecule inhibitor of c-Myc/Max dimerization. J Pharmacol Exp Ther. 2010 Dec;335(3):715-27.

[5]Follis AV, Hammoudeh DI, et al. Structural rationale for the coupled binding and unfolding of the c-Myc oncoprotein by small molecules. Chem Biol. 2008 Nov 24;15(11):1149-55.

10074-G5 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.01mL

0.60mL

0.30mL

15.05mL

3.01mL

1.50mL

30.09mL

6.02mL

3.01mL

10074-G5 技术信息

CAS号413611-93-5
分子式C18H12N4O3
分子量 332.31
SMILES Code O=[N+](C1=CC=C(NC2=CC=CC=C2C3=CC=CC=C3)C4=NON=C41)[O-]
MDL No. MFCD00576774
别名
运输蓝冰
InChI Key KMJPYSQOCBYMCF-UHFFFAOYSA-N
Pubchem ID 2836600
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place, sealed in dry, room temperature

溶解方案 请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
方案二
Ambeed 相关网站 Ambeed.cn Ambeed.com
Ambeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    Ambeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。