cetiedil

Known as: alpha-cyclohexyl-3-thiopheneacetic acid, 2-(hexahydro-1H-azepin-1-yl)ethyl ester 
 

Topic mentions per year

Topic mentions per year

1976-2013
024619762013

Papers overview

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2004
2004
Quinidine and Ba(2+), non-selective K(+)-channel blockers, have previously been shown to inhibit antigen-induced mediator (beta… (More)
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1989
1989
Synaptic vesicles purified on a sucrose-KCl sedimentation gradient were tested for their ability to accumulate [1-14C… (More)
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1989
1989
Cetiedil is a potent blocker of acetylcholine and choline fluxes. Several analogs of this compound have been synthesized and… (More)
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1987
1987
Cetiedil, a drug that is reported to block K+-channels, substantially increases the conductive C1- permeability of Chinese… (More)
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1986
1986
We have recently completed a double-blind, placebo-controlled, noncrossover study, the goal of which was to determine whether… (More)
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1986
1986
Cetiedil citrate is an antisickling agent shown to be effective in reducing the severity and duration of acute sickle cell crisis… (More)
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1984
1984
Two new vascular smooth muscle relaxants, bepridil and cetiedil, were found to possess specific CaM-inhibitory properties which… (More)
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1984
1984
Cetiedil, an in vitro anti-sickling agent, inhibited calmodulin-stimulated cyclic 3':5'-nucleotide phosphodiesterase (EC 3.1.4.17… (More)
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1981
1981
Cetiedil has been reported to relieve painful crises in sickle cell anemia and to have antisickling properties in vitro. The drug… (More)
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1980
1980
Cetiedil used clinically in cases of chronic cardiovascular disease in Europe was found to inhibit sickling and improve the… (More)
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