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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
ICA-105665 (PF-04895162) is a potent and orally active neuronal Kv7.2/7.3 and Kv7.3/7.5 potassium channels opener. ICA-105665 inhibits liver mitochondrial function and bile salt export protein (BSEP) transport ( IC 50 of 311 μM). ICA-105665 can penetrate
IC50& Target:Kv7.2/7.3 and Kv7.3/7.5 potassium channels
In Vitro:ICA-105665 (PF-04895162) does not display potent cytotoxic properties in THLE and HepG2 cell lines (IC 50 ~192 μM and 130 μM after 72 hours, respectively) or in human hepatocytes (AC 50 for cell loss at 48 hours was >125 μM based on results in three asses
In Vivo:For ICA-105665 (PF-04895162), in a 7-day rat toxicity study, dose-dependent alanine aminotransferase (ALT) elevations, potentially indicative of liver toxicity, were observed. However, no histological evidence of liver injury was identified, and ALT eleva
Biological Activity:ICA-105665 (PF-04895162) is a potent and orally active neuronal Kv7.2/7.3 and Kv7.3/7.5 potassium channels opener. ICA-105665 inhibits liver mitochondrial function and bile salt export protein (BSEP) transport ( IC 50 of 311 μM). ICA-105665 can penetrate
| Molecular Weight | 355.34 |
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