CAS NO: | 700-06-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
200mg | 电议 |
1 g | 电议 |
5 g | 电议 |
10 g | 电议 |
生物活性 |
Indole-3-carbinol (I3C) inhibitsNF-κBactivity and also is anAryl hydrocarbon receptor(AhR) agonist, and an inhibitor ofWWP1(WW domain-containing ubiquitin E3 ligase 1). |
||||||||||||||||
IC50& Target[1][2] |
|
||||||||||||||||
体外研究 (In Vitro) |
It is found that Indole-3-carbinol (I3C) inhibits the proliferation of THP-1 cells in a dose- and time dependent manner with minimal toxicity over normal monocytes. The AhR target genes (CYP1A1, IL1β) are overexpressed upon Indole-3-carbinol treatment (p<0.05 to p<0.001). The antiproliferative effects of Indole-3-carbinol are in association with programing cell death. Indole-3-carbinol downregulates BCL2 and upregulates FasR in THP-1 cells (p<0.05 to p<0.001). G1 cell cycle arrest is also observed using flow cytometry. G1-acting cell cycle genes (P21, P27 and P53) are overexpressed (p<0.05 to p<0.001), while CDK2 is downregulated upon Indole-3-carbinol treatment (p<0.01 to p<0.001)[1].Indole-3-carbinol suppresses NF-κB activity and stimulates the p53 pathway in pre-B acute lymphoblastic leukemia cells[2].
|
||||||||||||||||
Clinical Trial |
|
||||||||||||||||
分子量 |
147.17 |
||||||||||||||||
性状 |
Solid |
||||||||||||||||
Formula |
C9H9NO |
||||||||||||||||
CAS 号 |
700-06-1 |
||||||||||||||||
中文名称 |
3-吲哚甲醇 |
||||||||||||||||
结构分类 |
|
||||||||||||||||
来源 |
|
||||||||||||||||
运输条件 |
Room temperature in continental US; may vary elsewhere. |
||||||||||||||||
储存方式 |
|
||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 100 mg/mL(679.49 mM;Need ultrasonic)
配制储备液
*
请根据半岛bd体育手机客户端 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半岛bd体育手机客户端 失效。
In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro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,建议您现用现配,当天使用; 以下溶剂前显示的百
*
以上所有助溶剂都可在本网站选购。
|