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Merck
CN

P0032

Sigma-Aldrich

吡喃 3

≥98% (HPLC)

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别名:
乙基-1-(4-(2,3,3-三氯丙烯酰胺)苯基)-5-(三氟甲基)-1H-吡唑-4-羧酸酯
经验公式(希尔记法):
C16H11Cl3F3N3O3
分子量:
456.63
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.25

质量水平

检测方案

≥98% (HPLC)

形式

powder

颜色

white to beige

溶解性

DMSO: 20 mg/mL, clear

储存温度

2-8°C

SMILES字符串

CCOC(=O)c1cnn(-c2ccc(NC(=O)\C(Cl)=C(\Cl)Cl)cc2)c1C(F)(F)F

InChI

1S/C16H11Cl3F3N3O3/c1-2-28-15(27)10-7-23-25(12(10)16(20,21)22)9-5-3-8(4-6-9)24-14(26)11(17)13(18)19/h3-7H,2H2,1H3,(H,24,26)

InChI key

RZHGONNSASQOAY-UHFFFAOYSA-N

相关类别

生化/生理作用

Pyr3 是一种吡唑类化合物,可强效选择性拮抗 TRPC3。Pyr3 通过与受体胞外侧结合,抑制 TRPC3,从而抑制 B 细胞活化和心肌肥厚。

经典瞬时受体电位 (TRPC) 通道家族的成员是传导 Ca + 2 的离子通道,被膜受体介导的磷脂酶 C (PLC) 活性刺激激活。然而,TRPC3 和其他家族成员也被膜非依赖性甘油二酯 (DAG) 激活。BTP1 和 BTP2 是阻断 TRPC 通道的吡唑类药物,但它们对 TRPC 亚型无特异性。该通道参与多种过程,包括 B 细胞受体 (BCR) 介导的 Ca + 2 振荡、活化 T 细胞核因子 (NFAT) 的活化以及促进心肌肥厚。

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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