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Merck
CN

I2142

KN-62

≥95%, powder

别名:

(S)-5-异喹啉磺酸 4-[(2S)-2-[(5-异喹啉磺酰基)甲氨基]-3-氧代-3-(4-苯基-1-哌嗪基)丙基]苯酯, 1-[N,O-二(5-异喹啉磺酰基)-N-甲基-L-型酪氨酸]-4-苯基哌嗪

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关于此项目

经验公式（希尔记法）:
C38H35N5O6S2
化学文摘社编号:
127191-97-3
分子量:
721.84
MDL编号:
MFCD00083180
UNSPSC代码:
12352200
PubChem化学物质编号:
24895961
NACRES:
NA.77

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生物来源

synthetic (organic)

质量水平

200

方案

≥95%

表单

powder

颜色

yellow

mp

130 °C

溶解性

45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.93 mg/mL
methanol: 10 mg/mL
DMSO: 12 mg/mL
chloroform: 20 mg/mL

储存温度

−20°C

SMILES字符串

O=S(OC1=CC=C(C[C@@H](C(N2CCN(C3=CC=CC=C3)CC2)=O)N(C)S(C4=CC=CC5=C4C=CN=C5)(=O)=O)C=C1)(C6=CC=CC7=C6C=CN=C7)=O

InChI

1S/C38H35N5O6S2/c1-41(50(45,46)36-11-5-7-29-26-39-19-17-33(29)36)35(38(44)43-23-21-42(22-24-43)31-9-3-2-4-10-31)25-28-13-15-32(16-14-28)49-51(47,48)37-12-6-8-30-27-40-20-18-34(30)37/h2-20,26-27,35H,21-25H2,1H3/t35-/m0/s1

InChI key

RJVLFQBBRSMWHX-DHUJRADRSA-N

基因信息

human ... P2RX7(5027)

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相关类别

生化/生理作用

选择性抑制大鼠脑 Ca2+/钙调蛋白依赖性蛋白激酶 II。

特点和优势

《受体分类和信号转导手册》的 Ca/CaMKs和P2受体：P2X离子通道家族 页面有该化合物的介绍。想要浏览手册的其他页面， 请单击此处。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000323633
0000323633
0000371908
0000371907
0000332918

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Antagonists of the P2X(7) receptor. From lead identification to drug development.
Simon D Guile et al.
Journal of medicinal chemistry, 52(10), 3123-3141 (2009-02-05)
Safina Gadeock et al.
Biochimica et biophysica acta, 1798(11), 2058-2066 (2010-07-31)
The P2X7 receptor is an extracellular ATP-gated cation channel critical in inflammation and immunity, and can be up-regulated by IFN-γ and LPS. This study aimed to examine the effect of TGF-β1 on the up-regulation of P2X7 function and expression in
G H Fan et al.
Molecular pharmacology, 56(1), 39-45 (1999-07-01)
Learning and memory have been suggested to be important in the development of opiate addiction. Based on the recent findings that calcium/calmodulin-dependent protein kinase II (CaMKII) is essential in learning and memory processes, and morphine treatment increases CaMKII activity in
R J MacLeod et al.
The Journal of membrane biology, 172(1), 59-66 (1999-11-07)
To assess the activation of the charybdotoxin-insensitive K(+) channel responsible for Regulatory Volume Decrease (RVD) after substantial volume increases, we measured intracellular pH (pH(i)), intracellular calcium ([Ca(2+)](i)) and inhibitors of kinases and phosphoprotein phosphatases in guinea pig jejunal villus enterocytes
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