NMR studies of pyridine-N-oxide. Determination of spectroscopic constants from [15N]-, [4-2H], and the parent species

1978 ◽  
Vol 31 (2) ◽  
pp. 177-186 ◽  
Author(s):  
Torben Wamsler ◽  
Jørgen Tormod Nielsen ◽  
Erik Jonas Pedersen ◽  
Kjeld Schaumburg
1981 ◽  
Vol 43 (3) ◽  
pp. 387-398 ◽  
Author(s):  
Torben Wamsler ◽  
Jørgen Tormod Nielsen ◽  
Erik Jonas Pedersen ◽  
Kjeld Schaumburg

1987 ◽  
Vol 252 (4) ◽  
pp. C441-C449 ◽  
Author(s):  
L. A. Levy ◽  
E. Murphy ◽  
R. E. London

Fluorine 19 nuclear magnetic resonance (NMR) studies of intracellular fluorinated calcium chelators provide a useful strategy for the determination of cytosolic free calcium levels in cells and perfused organs. However, the fluorinated chelator with the highest affinity for calcium ions which has been described to date. 1,2-bis-(2-amino-5-fluorophenoxy)ethane-N,N,N',N'-tetraacetic acid (5FBAPTA), exhibits a dissociation constant (Kd) value 5- to 10-fold greater than the intracellular calcium concentration levels in most cell types, thus limiting the ability of fluorine NMR to report these concentrations reliably. We have consequently designed and synthesized several fluorinated calcium chelators with higher affinity for calcium. The best of these, 2-(2-amino-4-methyl-5-fluorophenoxy)-methyl-8 aminoquinidine-N,N,N',N'-tetraacetic acid (quinMF), has a Kd value approximately 10 times lower than that of 5FBAPTA. Several of the newly synthesized indicators have different chemical shifts for the calcium complexed and uncomplexed chelators to allow the simultaneous use of two indicators. In addition to providing information about the level of cytosolic free calcium, chelators containing a quinoline ring exhibit considerable sensitivity to magnesium levels and hence have potential application for the determination of cytosolic-magnesium concentrations. Application of these chelators is illustrated by determination of the cytosolic-free calcium level in erythrocytes. Use of quinMF, the chelator with the lowest Kd value, gives a calcium value of 25-30 nM.


2019 ◽  
Vol 221 (1) ◽  
pp. 1900327 ◽  
Author(s):  
Lars Gabriel ◽  
Wolfgang Günther ◽  
Friederike Pielenz ◽  
Thomas Heinze
Keyword(s):  

The microwave rotational spectrum of the hydrogen-bonded heterodimer CH 3 CN • • • HF has been identified and shown to be characteristic of a symmetric top. A detailed analysis of several rotational transitions for a variety of isotopic species gives the spectroscopic constants summarized in the following table: Rotational constants/MHz, vibration-rotation constants/MHz and vibrational separations/cm -1 of CH 3 CN • • • HF


1985 ◽  
Vol 63 (10) ◽  
pp. 2781-2786 ◽  
Author(s):  
Francis Michon ◽  
Jean Robert Brisson ◽  
René Roy ◽  
Harold J. Jennings ◽  
Fraser E. Ashton

The capsular polysaccharide antigen of Neisseriameningitidis group K was isolated by Cetavlon precipitation and purified by ion-exchange chromatography. The structure of the K polysaccharide was determined to a large extent by comprehensive proton and carbon-13 nuclear magnetic resonance (nmr) studies. In these studies one-dimensional and two-dimensional experiments were carried out directly on the K polysaccharide. The K polysaccharide is composed of the following repeating unit: -4)β-D-ManpNAcA(1→3) [4-OAc]β-D-ManpNAcA(1→. Except for the one-bond couplings between their anomeric carbons and protons [Formula: see text], all the nmr spectroscopic evidence was consistent with both 2-acetamido-2-deoxy-D-mannopyranosyluronic acid residues adopting the 4C1 (D) conformation and having the β-D-configuration. This ambiguity in [Formula: see text] is probably due to through-space electronic effects generated by the presence of contiguous carboxylated sugar residues in the K polysaccharide. The O-acetyl substituents of the K polysaccharide are essential for its antigenicity to group K polysaccharide-specific antibodies.


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