中文名称: MYCMI-6 促销
英文名称: MYCMI-6
CAS No: 681282-09-7
分子式: C20H19N7O
分子量: 373.41
M10787 MYCMI-6 ≥95% (psaitong)
包装规格:
5mg 10mg in glass bottle
溶解性:
溶于DMSO(2 mg/mL 超声)
产品描述:

基本信息

产品编号:M10787

产品名称:MYCMI-6

CAS:

681282-09-7

 

储存条件

粉末

-20℃

四年

 

 

分子式:

C20H19N7O

溶于液体

-80℃

六个月

分子量

373.41

-20℃

一个月

化学名: 

 

 

Solubility (25°C)

 

体外

DMSO

 

Ethanol

 

Water

 

体内(现配现用)

 

 

1mg/ml表示微溶或不溶。

普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。

 

制备储备液

 

浓度

 

溶液体积

质量

 

1mg

 

5mg

 

10mg

1mM

2.6780mL

13.3901mL

26.7802mL

5mM

0.5356mL

2.6780mL

5.3560mL

 

生物活性

产品描述

一种有效的选择性内源性 MYC:MAX 蛋白相互作用抑制剂。

靶点/IC50

c-Myc

Apoptosis

 

体外研究

MYCMI-6 (NSC354961) (6.25μM; 48 hours) selectively suppresses MYC-driven tumor cell growth with high efficacy.MYCMI-6 significantly inhibits growth of Burkitt’s lymphoma cells (Mutu,Daudi and ST486) - another classical example of a MYC-driven tumor, having translocations of MYC to one of the immunoglobulin loci - in a dose-dependent manner with an average GI50 of 0.5μM.Treatment of MCF7 cells with the MYCMI-6 for 24 hours significantly decreased MYC:MAX isPLA signals to 7%. Titration showed an IC50 for inhibition of MYC:MAX of less than 1.5μM for MYCMI-6 by isPLA. MYCMI-6 inhibits the MYC:MAX heterodimer formation with an IC50 of 3.8μM.MYCMI-6 efficiently inhibits anchorage-independent growth of MYCN-amplified neuroblastoma cells with GI50 values of <0.4μM.
Cell Viability Assay

Cell Line:

MYCN-amplified neuroblastoma cells (IMR-32, Kelly and SK-N-DZ), MYCN-non-amplified neuroblastoma cells (SK-N-F1, SK-N-AS and SK-N-RA)

Concentration:

6.25μM

Incubation Time:

48 hours

Result:

Result: Reduced growth of the MYCN-amplified cell lines significantly stronger than the MYCN-nonamplified cell lines.

体内研究

MYCMI-6 (20mg/kg; i.p.; daily for 1-2 weeks) induces massive apoptosis and reduces tumor cell proliferation, tumor microvasculature density and MYC:MAX interaction in a MYC-dependent xenograft tumor model.

Animal Model:

6-8 weeks old athymic nude mice (bearing MYCN-amplified SK-N-DZ neuroblastoma cells)

Dosage:

20 mg/kg body weight

Administration:

I.p.; daily for 1-2 weeks

Result:

A dramatic increase in the extension of apoptotic areas in the tumors and a significant increase in non-proliferative areas as determined by Ki67 staining in tumors.

保存条件:
-20℃
UN码:
HazardClass:
危害声明:
安全说明:
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参考文献 & 客户发表文献

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摩尔浓度计算公式

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    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
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    C8=C7/X C8: LOG(C8):