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Merck
CN

D5919

Sigma-Aldrich

二酰基甘油激酶抑制剂I

solid

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别名:
6-[2-[4-[(4-氟苯基)苯基亚甲基]-1-哌啶基]乙基]-7-甲基-5H-噻唑基-[3,2-a]-嘧啶-5-酮, R59022
经验公式(希尔记法):
C27H26FN3OS
CAS号:
分子量:
459.58
MDL编号:
UNSPSC代码:
41106300
PubChem化学物质编号:
NACRES:
NA.77

生物来源

synthetic (organic)

质量水平

检测方案

≥98% (HPLC)

形式

solid

颜色

pale yellow

溶解性

0.1 M HCl: slightly soluble
0.1 M NaOH: slightly soluble
DMSO: soluble
H2O: insoluble
ethanol: soluble
ethyl acetate: soluble

储存温度

−20°C

SMILES字符串

CC1=C(CCN2CCC(\CC2)=C(\c3ccccc3)c4ccc(F)cc4)C(=O)N5C=CSC5=N1

InChI

1S/C27H26FN3OS/c1-19-24(26(32)31-17-18-33-27(31)29-19)13-16-30-14-11-22(12-15-30)25(20-5-3-2-4-6-20)21-7-9-23(28)10-8-21/h2-10,17-18H,11-16H2,1H3

InChI key

MFVJXLPANKSLLD-UHFFFAOYSA-N

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一般描述

二酰基甘油激酶抑制剂I可防止异物巨细胞(FBGC)的形成。 它可抑制二酰基甘油磷酸化为磷脂酸。 二酰基甘油激酶抑制剂I可充当血清素(5-HT)受体(5-HTR)拮抗剂。它可刺激神经元细胞系NG108-15的凋亡和自噬。

应用

二酰基甘油激酶抑制剂I已被用作抑制剂用于使用高世代人类CAR(嵌合抗原受体)T细胞研究T细胞功能的抑制作用。

生化/生理作用

二酰基甘油激酶抑制剂。抑制红细胞膜中[38P]1-油酰基-2-乙酰甘油基-3-磷酸(OAPA)的形成:IC50 = 3.3 μM。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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