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SIRT2-IN-9
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
SIRT2-IN-9图片
CAS NO:522650-91-5
包装与价格:
包装价格(元)
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
SIRT2-IN-9 (compound 12) 是 SRIT2 的选择性抑制剂,IC50 值为 1.3 μM。SIRT2-IN-9 抑制 MCF-7 乳腺癌细胞的增殖活性。SIRT2-IN-9 可用于癌症的研究。
Cas No.522650-91-5
分子式C21H22N6OS2
分子量438.57
溶解度DMSO : 4.46 mg/mL (10.17 mM; ultrasonic and warming and heat to 70°C)
储存条件4°C, protect from light
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

SIRT2-IN-9 (compound 12) is a selective inhibitor ofSRIT2with anIC50value of 1.3 μM. SIRT2-IN-9 inhibits proliferative activity of MCF-7 breast cancer cells. SIRT2-IN-9 can be used for the research of cancer[1].

SIRT2-IN-9 (1-100 μM; 15 min) dose-dependently inhibits SRIT2 with an IC50value of 1.3 μM, and inhibits SRIT1 and SRIT3 with IC50s >300 μM[1].
SIRT2-IN-9 (0-50 μM; 72 h) affects cell viability of MCF-7 cells[1].
SIRT2-IN-9 (0-50 μM; 6 h) affects acetylation of α-tubulin protein[1].

Cell Proliferation Assay[1]

Cell Line:MCF-7 breast cancer cell line
Concentration:0-50 μM
Incubation Time:72 hours
Result:Dose-dependently inhibited cell proliferation of MCF-7 breast cancer cells.

Western Blot Analysis[1]

Cell Line:MCF-7 breast cancer cell line
Concentration:6.25, 12.5, 25 and 50 μM
Incubation Time:6 hours
Result:Dose-dependently increased acetylation of α-tubulin protein.