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insulin, N-methylpyridinium

Known as: Insulin, 19A-(O-(1-methylpyridinium-2-yl)-L-tyrosine)-, hydroxide, inner salt, N-methylpyridinium insulin 
 
National Institutes of Health

Papers overview

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2015
2015
Ultrafast electron transfer (ET) processes are important primary steps in natural and artificial photosynthesis, as well as in… Expand
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Highly Cited
2013
Highly Cited
2013
In the present paper we show a comprehensive in vitro, ex vivo and in vivo study on hydrolytic detoxification of nerve agent and… Expand
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2001
2001
In anhydrous CH3CN, 4-benzoyl-N-methylpyridinium cations undergo two reversible, well-separated (ΔE1/2 ∼ 0.6 V) one-electron… Expand
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1994
1994
A simple device for fluorescence measurements on kidney surface in situ (FKS) is described. The device consists of (1) an… Expand
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Highly Cited
1986
Highly Cited
1986
4-Phenyl-N-methylpyridinium (MPP+), the oxidation product of the neurotoxic amine MPTP, is considerably more inhibitory to the… Expand
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1979
1979
Reaction of insulin with 2-chloro- or 2-iodo-N-methylpyridinium iodide affords, amongst others, an insulin analogue modified at… Expand
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Highly Cited
1959
Highly Cited
1959
2‐Hydroxyiminomethyl‐N‐methylpyridinium methanesulphonate (P2S) is prepared by boiling pyridine‐2‐aldoxime with methyl… Expand
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1959
1959
The soluble methanesulphonate of the oxime 2-hydroxyiminomethyl-N-methylpyridinium (P2S) has been used to treat animals poisoned… Expand
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