NCX

抑制剂选择性比较

特异性亚型抑制剂

NCX产品

所有产品(7) NCX抑制剂(7)

目录号	产品描述	文献引用	实验数据
S4643	KB-R7943 mesylate KB-R7943 mesylate 是 Na+/Ca2+ exchanger (NCX(rev)) 的广泛使用的抑制剂，IC50值为5.7 μM。KB-R7943 mesylate 通过激活 JNK 途径和阻断自噬潮autophagic flux来促进前列腺癌细的死亡。
E0002^New	CGP-37157 CGP-37157 是一种有效、选择性和特异性的线粒体 Na(+)-Ca2+ exchanger 抑制剂，作用浓度 ≤ 10 μM。
S6920	SEA0400 SEA0400 是一种选择性的 Na+-Ca2+ exchanger (NCX) 的强效抑制剂，可抑制神经细胞、星形胶质细胞和小胶质细胞中Na+依赖性的Ca2+吸收，对应的IC50值分别为33 nM、5.0 nM和8.3 nM。SEA0400 可防止硝普钠 (SNP) 提高 ERK 和 p38 MAPK 的磷酸化和通过细胞外Ca2+依赖的方式增强reactive oxygen species (ROS) 的产生。
S3558	Benzamil Benzamil (Benzylamiloride), an analogue of amiloride, is a Na+/Ca2+ exhanger (NCX) inhibitor with IC50 of ~ 100 nM and an epithelial sodium channel (ENaC) blocker. Benzamil inhibits TRPP3-mediated Ca2+-activated currents with IC50 of 1.1 μM.
S0406	Benzylamiloride hydrochloride Benzamil hydrochloride is a potent and specific blocker of sodium channel (ENaC).
S4353	Terfenadine Terfenadine is an antihistamine, generally completely metabolizes to the active form fexofenadine in the liver by the enzyme cytochrome P450 CYP3A4 isoform. Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC50 of 204 nM. Terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca2+ homeostasis. Terfenadine induces ROS-dependent apoptosis, simultaneously activates Caspase-4, -2, -9.
S0016	SN-6 SN-6 是一种选择性的 Na+/Ca2+ exchanger (NCX) 抑制剂。SN-6 可抑制NCX1、NCX2和NCX3，对应的IC50值分别为2.9 μM、16 μM和8.6 μM。SN-6 可消除 acetylcholine (ACh) 诱导的血管舒张。

目录号	产品描述	文献引用	实验数据
S4643	KB-R7943 mesylate KB-R7943 mesylate 是 Na+/Ca2+ exchanger (NCX(rev)) 的广泛使用的抑制剂，IC50值为5.7 μM。KB-R7943 mesylate 通过激活 JNK 途径和阻断自噬潮autophagic flux来促进前列腺癌细的死亡。
E0002^New	CGP-37157 CGP-37157 是一种有效、选择性和特异性的线粒体 Na(+)-Ca2+ exchanger 抑制剂，作用浓度 ≤ 10 μM。
S6920	SEA0400 SEA0400 是一种选择性的 Na+-Ca2+ exchanger (NCX) 的强效抑制剂，可抑制神经细胞、星形胶质细胞和小胶质细胞中Na+依赖性的Ca2+吸收，对应的IC50值分别为33 nM、5.0 nM和8.3 nM。SEA0400 可防止硝普钠 (SNP) 提高 ERK 和 p38 MAPK 的磷酸化和通过细胞外Ca2+依赖的方式增强reactive oxygen species (ROS) 的产生。
S3558	Benzamil Benzamil (Benzylamiloride), an analogue of amiloride, is a Na+/Ca2+ exhanger (NCX) inhibitor with IC50 of ~ 100 nM and an epithelial sodium channel (ENaC) blocker. Benzamil inhibits TRPP3-mediated Ca2+-activated currents with IC50 of 1.1 μM.
S0406	Benzylamiloride hydrochloride Benzamil hydrochloride is a potent and specific blocker of sodium channel (ENaC).
S4353	Terfenadine Terfenadine is an antihistamine, generally completely metabolizes to the active form fexofenadine in the liver by the enzyme cytochrome P450 CYP3A4 isoform. Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC50 of 204 nM. Terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca2+ homeostasis. Terfenadine induces ROS-dependent apoptosis, simultaneously activates Caspase-4, -2, -9.
S0016	SN-6 SN-6 是一种选择性的 Na+/Ca2+ exchanger (NCX) 抑制剂。SN-6 可抑制NCX1、NCX2和NCX3，对应的IC50值分别为2.9 μM、16 μM和8.6 μM。SN-6 可消除 acetylcholine (ACh) 诱导的血管舒张。