| 產(chǎn)品詳情 |
| Edit |   |
|---|
| Product Name | SR 33805 oxalate |
|---|
| Description | Potent Ca2+ channel antagonist; binds allosterically to the a1-subunit of L-type Ca2+ channels (Kd = 20 pM), at a site distinct from other types of blocker. Shows some selectivity for vascular smooth muscle, inducing vasorelaxation without producing inotropic or chronotropic effects. Inhibits PDGF-stimulated smooth muscle cell proliferation. Purity 99%. MW (observed): 654.77 |
|---|
| Size | 10 mg |
|---|
| Concentration | n/a |
|---|
| Applications | n/a |
|---|
| Other Names | 3,4-Dimethoxy-N-methyl-N-[3-[4-[[1-methyl-3-(1-methylethyl)-1H-indol-2-yl]sulfonyl]phenoxy]propyl]benzeneethanamine |
|---|
| Gene, Accession, CAS # | CAS: 121346-33-6 |
|---|
| Catalog # | 1806/10 |
|---|
| Price | |
|---|
| Order / More Info | SR 33805 oxalate from TOCRIS BIOSCIENCE
|
|---|
| Product Specific References | PubMed: 18715900 |
|---|
| 產(chǎn)品資料 |
|
|