EPS002
MS-275
A HDAC1 and HDAC3 inhibitor
别名:
MS-275 (Entinostat, SNDX-275), 3-吡啶基甲基[[4-[[(2-氨基苯基)氨基]羰基]苯基]甲基]氨基甲酸酯, N-(2-氨基苯基)-4-[N-(吡啶-3-甲氧基羰基)氨甲基]苯甲酰胺
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关于此项目
经验公式（希尔记法）:
C21H20N4O3
CAS Number:
分子量:
376.41
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.41
方案
≥99%
溶解性
DMSO: 38 mg/mL
储存温度
−20°C
SMILES字符串
Nc1ccccc1NC(=O)c2ccc(CNC(=O)OCc3cccnc3)cc2
InChI
1S/C21H20N4O3/c22-18-5-1-2-6-19(18)25-20(26)17-9-7-15(8-10-17)13-24-21(27)28-14-16-4-3-11-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)
InChI key
INVTYAOGFAGBOE-UHFFFAOYSA-N
基因信息
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一般描述
优先于HDAC3（IC50=8 μM）抑制HDAC1（IC50 = 300nM）。 对HDAC8（IC50>100 μM）无抑制活性。
应用
MS-275已被用作组蛋白脱乙酰酶-1抑制剂。
生化/生理作用
HDAC抑制剂，抗增殖。
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral - Repr. 1A
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
历史批次信息供参考:
Marta Bombardo et al.
Scientific reports, 8(1), 9391-9391 (2018-06-22)
Adult pancreatic acinar cells have the ability to re-enter the cell cycle and proliferate upon injury or tissue loss. Despite this mitotic ability, the extent of acinar proliferation is often limited and unable to completely regenerate the injured tissue or
HoxC5 and miR-615-3p target newly evolved genomic regions to repress hTERT and inhibit tumorigenesis
TingDong Y et al.
Nature Communications, 100 (2018)
Guido Dentesano et al.
Journal of neuroinflammation, 9, 165-165 (2012-07-11)
In physiological conditions, it is postulated that neurons control microglial reactivity through a series of inhibitory mechanisms, involving either cell contact-dependent, soluble-factor-dependent or neurotransmitter-associated pathways. In the current study, we focus on CD200R1, a microglial receptor involved in one of
Heather MacTavish et al.
PloS one, 5(12), e14462-e14462 (2011-02-02)
Histone deacetylase inhibitors (HDI) dampen cellular innate immune response by decreasing interferon production and have been shown to increase the growth of vesicular stomatitis virus and HSV. As attenuated tumour-selective oncolytic vaccinia viruses (VV) are already undergoing clinical evaluation, the
Xuelian Xu et al.
PloS one, 6(2), e17138-e17138 (2011-03-02)
Pediatric acute myeloid leukemia (AML) remains a challenging disease to treat even with intensified cytarabine-based chemotherapy. Histone deacetylases (HDACs) have been reported to be promising therapeutic targets for treating AML. However, HDAC family members that are involved in chemotherapy sensitivities
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