所有图片(1)
About This Item
经验公式（希尔记法）:
C20H16N2O6
CAS号:
分子量:
380.35
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
质量水平
检测方案
≥98% (HPLC)
形式
powder
颜色
off-white to light tan
溶解性
DMSO: ≥20 mg/mL
储存温度
2-8°C
SMILES字符串
Oc1cccc(C(=O)Nc2cccc(NC(=O)c3cccc(O)c3O)c2)c1O
InChI
1S/C20H16N2O6/c23-15-8-2-6-13(17(15)25)19(27)21-11-4-1-5-12(10-11)22-20(28)14-7-3-9-16(24)18(14)26/h1-10,23-26H,(H,21,27)(H,22,28)
InChI key
MIQUEZGHEJGPJB-UHFFFAOYSA-N
应用
MST-312已被用于利用小鼠成纤维细胞（NIH-3T3）的细胞侵袭检测以及结肠成纤维细胞中的免疫共沉淀实验。
生化/生理作用
MST-312是一种端粒酶抑制剂。端粒是存在于染色体末端的核蛋白复合物，含有会随着每个重复的细胞周期而缩短DNA片段串联重复序列。端粒缩短可引起功能的丧失，从而导致细胞衰老和有限的生存能力。逆转录酶端粒酶在永生化细胞系和大多数癌细胞系中维持着端粒的长度和功能，而端粒酶的活性也与肿瘤的发生有关。端粒延长也被认为是促进iPS细胞基因组稳定性和无限自我更新的重要因素。1 μM MST-312已显示出在U937细胞中能够有效缩短端粒长度并对增殖进行抑制。
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Laurent Lacroix et al.
Nucleic acids research, 39(4), e21-e21 (2010-11-26)
RNA and DNA guanine-rich sequences can adopt unusual structures called Guanine quadruplexes (G4). A quadruplex-prone RNA sequence is present at the 5'-end of the 451-nt-long RNA component of telomerase, hTERC. As this quadruplex may interfere with P1 helix formation, a
Salinomycin abolished STAT3 and STAT1 interactions and reduced telomerase activity in colorectal cancer cells.
Chung SS, et al.
Anticancer Research, 37(2), 445-453 (2017)
Combination treatment with flavonoid morin and telomerase inhibitor MST-312 reduces cancer stem cell traits by targeting STAT3 and telomerase.
Chung SS, et al.
International Journal of Oncology, 49(2), 487-498 (2016)
Yancong Kong et al.
The Analyst, 144(15), 4694-4701 (2019-07-04)
The development of facile and sensitive miRNA quantitative detection methods is a central challenge for the early diagnosis of miRNA-related diseases. Herein, we propose a strategy for a liposome-encoded magnetic bead-based DNA toehold-mediated DNA circuit for the simple and sensitive
Ponmathi Panneerpandian et al.
Antiviral research, 174, 104695-104695 (2019-12-18)
Yin Yang 1 (YY1) is a ubiquitous transcription factor with both transcriptional activating and repressing functions. Targeting YY1 is considered as a potential therapeutic strategy for several malignancies. Telomerase Reverse Transcriptase (TERT) is also considered as a potential target for
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