Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12219 |
NHE3-IN-1
|
Sodium Channel | Membrane transporter/Ion channel |
NHE3-IN-1 是钠/质子交换剂 3 (NHE-3) 的抑制剂。 | |||
T61480 | NHE3-IN-3 | ||
NHE3-IN-3 (Compound 1) is a potent inhibitor of the isoform 3 of the Na+/H+ exchanger (NHE3). It exhibits pIC50 values of 6.2 and 6.6 against human and rat NHE3, respectively. Furthermore, NHE3-IN-3 showcases exceptional oral bioavailability of 98% in Sprague–Dawley rats [1]. | |||
T60652 |
NHE3-IN-2
|
||
NHE3-IN-2 是Na+/H+交换体 3(NHE3)的抑制剂 。 | |||
TQ0157 |
EIPA
L593754,MH 12-43 |
Sodium Channel; TRP/TRPV Channel | Membrane transporter/Ion channel |
EIPA (L593754) 是一种有效的TRPP3 channel 抑制剂,IC50为 10.5 μM。EIPA 对Na+/H+交换 (NHE) 和巨噬细胞也有抑制作用。 | |||
T7587 |
Tenapanor
RDX-5791,RDX 5791,AZD 1722,Tenapanor free base,RDX5791,AZD-1722,AZD1722 |
Sodium Channel | Membrane transporter/Ion channel |
Tenapanor (RDX 5791) 是钠氢离子交换NHE3的有效抑制剂, 对人和大鼠NHE3的IC50分别是5和10 nM。 | |||
T7587L |
Tenapanor HCl
RDX-5791,AZD 1722,AZD-1722,AZD1722,RDX5791,RDX 5791 |
||
Tenapanor( AZD-1722, RDX 5791) is an inhibitor of the sodium-proton (Na(+)/H(+)) exchanger NHE3, which is used for sodium handling in the gastrointestinal tract and kidney. |