所有图片(1)
About This Item
经验公式（希尔记法）:
C20H20N6S4
CAS号:
分子量:
472.67
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77
推荐产品
化驗
≥95% (HPLC)
形狀
powder
儲存條件
desiccated
顏色
white
溶解度
DMSO: >5 mg/mL
H2O: insoluble
儲存溫度
2-8°C
SMILES 字串
S=C=Nc1cccc(NC(=S)NCCCCNC(=S)Nc2cccc(c2)N=C=S)c1
InChI
1S/C20H20N6S4/c27-13-23-15-5-3-7-17(11-15)25-19(29)21-9-1-2-10-22-20(30)26-18-8-4-6-16(12-18)24-14-28/h3-8,11-12H,1-2,9-10H2,(H2,21,25,29)(H2,22,26,30)
InChI 密鑰
QOHNRGHTJPFMSL-UHFFFAOYSA-N
應用
MRS 2578 已作为嘌呤受体 P2Y6 的拮抗剂被用于：
- 研究嘌呤能受体在 Up4A 诱导猪冠状小动脉舒张中的作用
- 在铜绿假单胞菌感染的小鼠中测试其对炎症反应的影响
- 测试其对多形核白细胞中中性粒细胞胞外陷阱和单钠尿酸盐 (MSU) 晶体形成的抑制作用
生化／生理作用
在体外和体内条件下，MRS 2578 可在神经母细胞瘤细胞中引发细胞保护功能并防止多巴胺能神经元的死亡。它还可通过延迟脂多糖诱导的死亡来保护小胶质细胞。
P2Y6 核苷酸受体强效且不可逆的拮抗剂。
特點和優勢
该化合物的相关信息整理于受体分类和信号转导手册的 P2受体：P2Y G蛋白家族 页面。想要浏览手册的其他页面， 请单击此处。
訊號詞
Danger
危險分類
Acute Tox. 3 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Junbo Zheng et al.
Respiratory research, 19(1), 190-190 (2018-10-01)
Pneumonia is a major cause of high morbidity and mortality in critically illness, and frequently requires support with mechanical ventilation. The latter can lead to ventilator-induced lung injury characterized by neutrophil infiltration. The cationic human neutrophil peptides (HNP) stored in
Liaman K Mamedova et al.
Biochemical pharmacology, 67(9), 1763-1770 (2004-04-15)
The physiological role of the P2Y(6) nucleotide receptor may involve cardiovascular, immune and digestive functions based on the receptor tissue distribution, and selective antagonists for this receptor are lacking. We have synthesized a series of symmetric aryl diisothiocyanate derivatives and
Ágatha Oliveira-Giacomelli et al.
Frontiers in cellular neuroscience, 13, 476-476 (2019-12-04)
Parkinson's disease (PD) is a neurodegenerative disorder characterized by decreased dopamine bioavailability in the substantia nigra and the striatum. Taking into account that adenosine-5'-triphosphate (ATP) and its metabolites are intensely released in the 6-hydroxydopamine (6-OHDA) animal model of PD, screening
Zhichao Zhou et al.
Purinergic signalling, 13(3), 319-329 (2017-05-26)
We previously demonstrated that uridine adenosine tetraphosphate (Up4A) induces potent and partially endothelium-dependent relaxation in the healthy porcine coronary microvasculature. We subsequently showed that Up4A-induced porcine coronary relaxation was impaired via downregulation of P1 receptors after myocardial infarction. In view
Tamara C Hornik et al.
Journal of cell science, 129(1), 65-79 (2015-11-15)
Some apoptotic processes, such as phosphatidylserine exposure, are potentially reversible and do not necessarily lead to cell death. However, phosphatidylserine exposure can induce phagocytosis of a cell, resulting in cell death by phagocytosis: phagoptosis. Phagoptosis of neurons by microglia might
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