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fantofarone

Known as: 2-isopropyl-1-((4-(3-(N-methyl-N-(3,4-dimethoxy-beta-phenethyl)amino)propoxy)benzenesulfonyl))indolizine, Benzeneethanamine, 3,4-dimethoxy-N-methyl-N-(3-(4-((2-(1-methylethyl)-1-indolizinyl)sulfonyl)phenoxy)propyl)- 
 
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Neutrophils rapidly undergo spontaneous apoptosis following their release from the bone marrow. Although central to leukocyte… Expand
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1999
1999
AIMS To investigate the pharmacokinetics of SR 33671, the main active metabolite of the calcium antagonist fantofarone, and the… Expand
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1998
1998
This study describes the synergistic interaction of two calcium channel blockers, verapamil (VR) and SR33557 or fantofarone (SR… Expand
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1997
1997
Mibefradil is a novel Ca2+ antagonist acting on both L- and T-type Ca2+ channels, with a ten-fold selectivity for T-type Ca2… Expand
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1995
1995
The possible activity of SR 33805 ([[N-[dimethoxy-3,4-phenethyl]-N- methylamino-propoxyl]-4-benzenesulfonyl]-2-isopropyl-3-methyl… Expand
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1994
1994
Using the fluorescent properties of fantofarone, we have studied the interactions between this novel calcium entry blocker and… Expand
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1994
1994
Fantofarone (SR33557) is a substituted indolizine and SR33805 is a substituted indole. These drugs have been shown to… Expand
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1994
1994
SR33557 (fantofarone) and SR33805 are structurally novel calcium antagonists that bind selectively to the alpha 1-subunit of the… Expand
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1994
1994
The biochemical and mechanical effects of a new calcium ion channel antagonist, fantofarone ((2-isopropyl-1-((4-(3-(N-methyl-N-(3… Expand
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1993
1993
In this study, SR 33805 was shown to inhibit competitively [3H]fantofarone binding to cardiac sarcolemmal membranes. In contrast… Expand
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