Skip to search formSkip to main contentSkip to account menu

NC 1100

Known as: NC-1100 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

tamolarizine

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1995
1995
Physiological Results of Monkey Brain Ischemia, and Protection by a Calcium Blocker
1995
1995
Synthesis and structure-activity relationships of 2-(4-benzhydryl-1-piperazinyl)-1-phenylethanols as new calcium blockers.
A series of 2-(4-benzhydryl-1-piperazinyl)-1-phenylethanols (4) was synthesized and evaluated for calcium entry-blocking activity… 
1992
1992
A new type of Ca2+ channel blocker, NC-1100, inhibits the low- and high-threshold Ca2+ currents in the rat CNS neurons
1992
1992
Attenuation of ischemic and postischemic damage to brain metabolism and circulation by a novel Ca2+ channel antagonist, NC-1100, in spontaneously hypertensive rats.
1992
1992
Attenuation of ischemic and postischemic damage to brain metabolism and circulation by a novel Ca2+ channel antagonist, NC-1100, in spontaneously hypertensive rats.
1991
1991
[Effects of 1-(3,4-dimethoxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol dihydrochloride (NC-1100) on the central nervous system].
The effects of NC-1100 on the central nervous system were analyzed behaviorally and electroencephalographically in mice, rabbits… 
1990
1990
Stereoselectivity of NC-1100, a Ca-entry blocker.
1989
1989
Effect of NC-1100 [1-(3,4-dimethoxyphenyl)-2-(4-diphenylmethylpiperazinyl) ethanol dihydrochloride] on gamma-aminobutyric acid (GABA) metabolism in rat brain: analysis using stroke-prone…
Effects of oral administration of NC-1100 on the metabolism of neuroactive amino acids in rat brain were studied using stroke… 
1989
1989
Cardiovascular effects of 1-(3,4-dimethoxyphenyl)-2-(4-diphenylmethylpiperazinyl) ethanol and possible mechanisms involved.
Cardiovascular effects of NC-1100 (1-(3,4-dimethoxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol and possible modes of action… 
1986
1986
Selectivity of cerebral vasodilators on basilar arteries.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)