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Medchemexpress LLC Benzeneethanamine, 3,4-dimethoxy-N-methyl-N-[3-[4-[[1-methyl-2-(1-methylethyl)-1H-indol-3-yl]sulfonyl] | 121345-64-0 | 99.8% | 564.74 | 50 MG

Supplier: Medchemexpress LLC HY13690950MG
SR33805 is a potent Ca2+ channel antagonist with EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively. It selectively blocks L-type but not T-type Ca2+ channels, making it suitable for research on acute or chronic failing hearts.
- Potent Ca2+ channel antagonist.
- Selectively blocks L-type Ca2+ channels.
- Useful for research on acute or chronic failing hearts.
- Inhibits growth factor-induced proliferation of smooth muscle cells (SMC) in vitro in a dose-dependent manner.
- Restores myocardial infarction (MI)-altered cell shortening without affecting Ca2+ transient amplitude in vitro.
- Improves end-systolic strain and fractional shortening of MI hearts in rats in vivo.
- Significantly reduces intimal hyperplasia in pigs in vivo.
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