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- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
925432-73-1
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1072.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥419.0 |
| 规格: | 5 mg | 产品价格: | ¥960.0 |
| 规格: | 10 mg | 产品价格: | ¥1435.0 |
| 规格: | 25 mg | 产品价格: | ¥2146.0 |
| 规格: | 50 mg | 产品价格: | ¥3206.0 |
| 规格: | 100 mg | 产品价格: | ¥4810.0 |
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SRT 1460
CAS No. : 925432-73-1
MCE 国际站:SRT 1460
产品活性:SRT 1460 是一种有效的 Sirtuin-1 (SIRT1) 激动剂,其 EC1.5 值为 2.9 μM。与对 SIRT2 和 SIRT3 (EC1.5>300 μM) 相比,SRT 1460 对 SIRT1 有很好的选择性,并且比白藜芦醇和相近 sirtuin 同系物更为有效。
研究领域:Cell Cycle/DNA Damage | Epigenetics
作用靶点:Sirtuin
In Vitro: SRT 1460 (2-6 μM; 72 hours) inhibits cell viability in a dose-dependent manner, with all pancreatic cancer cells being more sensitive than the control HPDE cell. The IC50s of those cells are: Patu8988t, 1.62±0.13 μM; SU86.86, 2.31±0.23 μM; Panc-1, 0.66 ±0.02 μM; HPDE, 2.39±0.29 μM.
?SRT 1460 (5 μM; 16 hours) increases expression of the autophagy marker LC3-II.
相关产品:Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Epigenetics Compound Library | Histone Modification Research Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Antioxidant Compound Library | Oxygen Sensing Compound Library | Glutamine Metabolism Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Obesity Compound Library | Highly Selective Activators Library | Nicotinamide | Resveratrol | Selisistat | 3-TYP | Nicotinamide riboside chloride | Fisetin | OSS_128167 | Suramin sodium salt | SRT 1720 | UBCS039 | AGK2 | Sirtinol | SRT 2104 | SIRT7 inhibitor 97491 | Thiomyristoyl | Tenovin-6 | MC3482 | SirReal2 | Cambinol | SRT 2183 | Ganoderic acid D | SIRT5 inhibitor 1 | AK-7 | Agrimol B | CAY10602 | SIRT-IN-3 | ADTL-SA1215 | Perindopril erbumine | Tenovin-1
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文献和实验loops by gene mutation enhances SRT synthesis. We demonstrate that gene loop conformation enforces transcriptional directionality on otherwise bidirectional promoters.
3' (三)血友病APCR基因诊断程序 1.母亲、先证者的RFLP及Amp-FLP,确定风险染色体 2.检测胎儿性别(SRT) 3.检测胎儿的RFLP及AmP-FLP 四、散发病例FVⅢ基因突变的PCR检测 由于因子FVⅢ的基因突变以点突变为主,而且具有高度特异性,因此,单独网点 突变的检测方法仍以诊断,对于形发病例来说,可用PCR-SSCP,PCR-DGGE及其它的点 突变是筛查方法确定点突变血友病A之间的关系具有重要意义,尤其是PCR
HPLC‐SEC Characterization of Membrane Protein‐Detergent Complexes
Figure 29.5.5 Optimization of HPLC‐SEC: impact of column pre‐equilibration with a buffer containing high detergent concentration. A Sepax SRT‐500 column, 7.8 × 300 mm, was used for fractionation. Dashed line
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