121346-32-5

Basic information

• Product Name: 3,4-DIMETHOXY-N-METHYL-N-[3-[4-[[1-METHYL-3-(1-METHYLETHYL)-1H-INDOL-2-YL]SULFONYL]PHENOXY]PROPYL]BENZENEETHANAMINE OXALATE
• Synonyms: 3,4-DIMETHOXY-N-METHYL-N-[3-[4-[[1-METHYL-3-(1-METHYLETHYL)-1H-INDOL-2-YL]SULFONYL]PHENOXY]PROPYL]BENZENEETHANAMINE OXALATE;SR 33805 OXALATE;3,4-Dimethoxy-N-methyl-N-(3-(4-((1-methyl-3-(1-methylethyl)-1H-indol-2-yl)sulfonyl)phenoxy)propyl)benzeneethanamineoxal];3,4-Dimethoxy-N-methyl-N-[3-[4-[[1-methyl-3-(1-methylethyl)-1H-indol-2-yl]sulfonyl]phenoxy]propyl]benzeneethanamine;N-(3,4-dimethoxyphenethyl)-3-(4-(3-isopropyl-1-methyl-1H-indol-2-ylsulfonyl)phenoxy)-N-methylpropan-1-amine;N-(3,4-Dimethoxyphenethyl)-3-(4-((3-isopropyl-1-methyl-1H-indol-2-yl)sulfonyl)phenoxy)-N-methylpr;N-(3,4-Dimethoxyphenethyl)-3-(4-((3-isopropyl-1-methyl-1H-indol-2-yl)sulfonyl)phenoxy)-N-methy;N-(3,4-Dimethoxyphenethyl)-3-(4-((3-isopropyl-1-methyl-1H-indol-2-yl)sulfonyl)phenoxy)-N-methylpropan-1-amine oxalate
• CAS NO: 121346-32-5
• Molecular Formula: C34H42N2O9S
• Molecular Weight: 654.77
• Product Categories: Calcium channel
• Mol File: 121346-32-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 728.7°C at 760 mmHg
• Flash Point: 394.5°C
• Appearance: /
• Density: 1.15±0.1 g/cm3(Predicted)
• Vapor Pressure: 4.34E-21mmHg at 25°C
• Storage Temp.: Store at RT
• PKA: 8.82±0.50(Predicted)
• CAS DataBase Reference: 3,4-DIMETHOXY-N-METHYL-N-[3-[4-[[1-METHYL-3-(1-METHYLETHYL)-1H-INDOL-2-YL]SULFONYL]PHENOXY]PROPYL]BENZENEETHANAMINE OXALATE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIMETHOXY-N-METHYL-N-[3-[4-[[1-METHYL-3-(1-METHYLETHYL)-1H-INDOL-2-YL]SULFONYL]PHENOXY]PROPYL]BENZENEETHANAMINE OXALATE(121346-32-5)
• EPA Substance Registry System: 3,4-DIMETHOXY-N-METHYL-N-[3-[4-[[1-METHYL-3-(1-METHYLETHYL)-1H-INDOL-2-YL]SULFONYL]PHENOXY]PROPYL]BENZENEETHANAMINE OXALATE(121346-32-5)

Safety Data

• Hazardous Substances Data: 121346-32-5(Hazardous Substances Data)

Usage

Uses

SR 33805 Oxalate is a potent calcium entry blocker.

Biological Activity

Potent Ca 2+ channel antagonist; binds allosterically to the a 1 -subunit of L-type Ca 2+ channels (K d = 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.

InChI:InChI=1/C31H38N2O5S.C3H4O4/c1-22(2)30-26-9-6-7-10-27(26)32-31(30)39(34,35)25-14-12-24(13-15-25)38-20-8-18-33(3)19-17-23-11-16-28(36-4)29(21-23)37-5;4-2(5)1-3(6)7/h6-7,9-16,21-22,32H,8,17-20H2,1-5H3;1H2,(H,4,5)(H,6,7)