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SID 3712249
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。
SID 3712249图片
CAS NO:522606-67-3
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品名称
MiR-544 Inhibitor 1
产品介绍
SID 3712249 (MiR-544 Inhibitor 1) 是一种miR-544生物合成抑制剂。SID 3712249 直接与前体 miRNA 结合。SID 3712249 阻断成熟 microRNA 的产生并减少 miR-544、HIF-1α 和 ATM 转录物。SID 3712249 可用于癌症研究。
生物活性

SID 3712249 (MiR-544 Inhibitor 1) is amiR-544biogenesis inhibitor. SID 3712249 binds directly to the precursor miRNA. SID 3712249 blocks production of the maturemicroRNAand decreases miR-544, HIF-1α, andATMtranscripts. SID 3712249 can be used in the research of cancers, such as breastcancer[1].

IC50& Target

MiR-544[1]

体外研究
(In Vitro)

SID 3712249 (compound 1, 20 nM, 48 h) disrupts miR-544-mediated inhibition of BMI1 based on significant increases in the RFP/BFP ratio[1].
SID 3712249 (20 nM, 48 h) inhibits precursor but not mature miR-544 binding to BMI1 or mTOR3’-UTR[1].
SID 3712249 (20 nM, 48 h) results in accumulation of pre-miR-544 and a decrease in miR-544 levels in MCF10A cells[1].
SID 3712249 (20 nM, 5 days) induces apoptosis in MDA-MB-231 and MCF- 7 cells and has no effect on cell survival in normoxic conditions[1].

Apoptosis Analysis[1]

Cell Line:MDA-MB-231, MCF-7 cells
Concentration:20 nM
Incubation Time:5 days
Result:Induced apoptosis and has no effect on cell survival in normoxic conditions (flow cytometric analysis of Annexin V and PI stainning).
体内研究
(In Vivo)

SID 3712249 (compound 1, 100 μL of 40 μM, intraperitoneal injection) inhibited tumor growth in MDA-MB-231-GFP-luc tumor model[1].
SID 3712249 (20 nM, pre-treated GFP-labeled MDA-MB-231 cells, intraperitoneal injection) inhibited tumor growth in MDA-MB-231-GFP-luc tumor model[1].

Animal Model:MDA-MB-231-GFP-luc tumor model[1]
Dosage:100 μL of 40 μM
Administration:Intraperitoneal injection
Result:Inhibited tumor growth (evidenced by live animal bioluminescent imaging) with no overt side effects.
Decreased levels of miR-544, ATM, and HIF-1α and increased levels of mTOR (resected tumor samples).
分子量

323.40

性状

Solid

Formula

C17H21N7

CAS 号

522606-67-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 16.67 mg/mL(51.55 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.0921 mL15.4607 mL30.9215 mL
5 mM0.6184 mL3.0921 mL6.1843 mL
10 mM0.3092 mL1.5461 mL3.0921 mL
*

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
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。