220 MHz spectra of heparin, chondroitins, and other mucopolysaccharides

1970 ◽  
Vol 48 (14) ◽  
pp. 2260-2268 ◽  
Author(s):  
A. S. Perlin ◽  
B. Casu ◽  
G. R. Sanderson ◽  
L. F. Johnson

Characteristics of proton magnetic resonance spectra of heparins at 220 MHz, coupled with spectral data for model compounds and with information obtained chemically, indicate that heparins are composed principally of (1 → 4)-linked α-L-idopyranosyluronic acid residues (3) and 2-amino-2-deoxy-α-D-glucopyranosyl residues (1); also, that sulfate groups are located at position -2 and -6 of 1, and -2 of 3. D-Glucopyranosyluronic acid residues (2) appear to be minor constituents, which is at variance with all structures that have been proposed previously for heparin.Spectra of chondroitins A, B, and C, which are readily distinguishable, are in close accord with formulae that have been proposed for these mucopolysaccharides; on the same basis, the spectrum of keratan sulfate is less consistent. Hyaluronic acid affords a poorly resolved though, nonetheless, distinctive spectrum. The general view that mucopolysaccharides are constituted basically of residues of hexosamine and uronic acid in equimolar proportion receives support from the current findings. However, heparitin appears to possess a more heterogeneous type of structure than do these other polymers.

1967 ◽  
Vol 20 (8) ◽  
pp. 1663 ◽  
Author(s):  
JFK Wilshire

2-Fluoro-5-nitrobenzonitrile, an analogue of 1-fluoro-2,4- dinitrobenzene, in which the 2-nitro group has been replaced by a cyano group, has been prepared and made to react with several amines, amino acids, and NH-heteroaromatic compounds. The proton magnetic resonance spectra of some of the resultant N-(2-cyano-4-nitrophenyl) derivatives were compared with the spectra of the corresponding N-(2,4- dinitrophenyl) derivatives and furnish further evidence that the ortho nitro group of the latter derivatives is rotated out of the plane of the aromatic nucleus.


1976 ◽  
Vol 59 (5) ◽  
pp. 1162-1169
Author(s):  
Keith Bailey ◽  
Denise R Gagné ◽  
Richard K Pike

Abstract The qualitative analysis of the aromatic bromination products of the 6 isomeric dimethoxyamphetamines and their hydrochloride or hydrobromide salts is described. Their ultraviolet, mass, and proton magnetic resonance spectra are not sufficiently different for distinction but infrared spectra allow a positive identification to be made and reference spectra are provided for the bromination products of 2,4-, 2,5-, 2,6-, 4,5-, and 3,5-dimethoxyamphetamines. The application of gas-liquid and thin layer chromatography for the analysis of these products is discussed. The bromination of 2,3-dimethoxyamphetamine consistently gave mixtures which could not be separated satisfactorily; spectra are included for completeness of the comparison of products.


1972 ◽  
Vol 4 (3) ◽  
pp. 441-442 ◽  
Author(s):  
Masako Ueyama ◽  
Kazuo Tori ◽  
Masaru Fukuyama

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