2250019-90-8

2250019-90-8 structure
2250019-90-8 structure
  • Name: Ned-K
  • Chemical Name: Ned-K
  • CAS Number: 2250019-90-8
  • Molecular Formula: C31H31N5O3
  • Molecular Weight: 521.61
  • Catalog: Signaling Pathways Membrane Transporter/Ion Channel Calcium Channel
  • Create Date: 2021-01-09 18:36:50
  • Modify Date: 2024-01-09 11:43:36
  • Ned-K is a nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist. Ned-K is effective at dampening simulated ischaemia and reperfusion (sIR)-induced Ca2+ oscillations in cardiomyocytes[1].

Name Ned-K
Description Ned-K is a nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist. Ned-K is effective at dampening simulated ischaemia and reperfusion (sIR)-induced Ca2+ oscillations in cardiomyocytes[1].
Related Catalog
In Vitro Ned-K suppresses Ca2+ oscillations and dramatically protects cardiomyocytes from cell death in vitro after ischaemia and reoxygenation, preventing opening of the mitochondrial permeability transition pore. Ned-K (10 µM) almost completely eliminates [Ca2+]c oscillations, and Ned-K (0.1 µM) is effective at suppressing [Ca2+]c levels[1]. Cell Viability Assay[1] Cell Line: Dead primary adult cardiomyocytes Concentration: 0.1 and 10 µM Incubation Time: Result: Treatment with 0.1 µM caused a slight decrease in cardiomyocyte death (34±6%). Treatment with 10 μM at reoxygenation significantly decreased cell death after sIR to 16±1%.
In Vivo Injection of Ned-K causes a significant reduction in infarct size in mice. Ned-K (administered i.v. to mice 5 min before reperfusion) significantly decreases myocardial infarct size relative to area at risk[1].
References

[1]. Sean M Davidson, et al. Inhibition of NAADP signalling on reperfusion protects the heart by preventing lethal calcium oscillations via two-pore channel 1 and opening of the mitochondrial permeability transition pore. Cardiovasc Res. 2015 Dec 1;108(3):357-66.

Molecular Formula C31H31N5O3
Molecular Weight 521.61
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.