63059-56-3Relevant academic research and scientific papers
NOVEL 5-SUBSTITUTED BENZIMIDAZOLIUM COMPOUNDS
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Paragraph 0186, (2015/02/18)
The present invention relates to compounds of general formula (I) and the tautomers and the salts thereof, particularly the pharmaceutically acceptable salts thereof with inorganic or organic acids and bases, which have valuable pharmacological properties, particularly an inhibitory effect on epithelial sodium channels, the use thereof for the treatment of diseases, particularly diseases of the lungs and airways.
NOVEL 5-SUBSTITUTED BENZIMIDAZOLIUM COMPOUNDS
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Page/Page column 40; 41, (2015/02/02)
The present invention relates to compounds of general formula (I) and the tautomers and the salts thereof, particularly the pharmaceutically acceptable salts thereof with inorganic or organic acids and bases, which have valuable pharmacological properties, particularly an inhibitory effect on epithelial sodium channels, the use thereof for the treatment of diseases, particularly diseases of the lungs and airways.
NOVEL TETRA- AND PENTASUBSTITUTED BENZIMIDAZOLIUM COMPOUNDS
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Paragraph 0170; 0172, (2015/02/18)
The present invention relates to compounds of general formula (I) and the tautomers and the salts thereof, particularly the pharmaceutically acceptable salts thereof with inorganic or organic acids and bases, which have valuable pharmacological properties, particularly an inhibitory effect on epithelial sodium channels, the use thereof for the treatment of diseases, particularly diseases of the lungs and airways.
NOVEL TETRA- AND PENTASUBSTITUTED BENZIMIDAZOLIUM COMPOUNDS
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Page/Page column 33; 34, (2015/02/02)
The present invention relates to compounds of general formula (I), and the tautomers and the salts thereof, particularly the pharmaceutically acceptable salts thereof with inorganic or organic acids and bases, which have valuable pharmacological properties, particularly an inhibitory effect on epithelial sodium channels, the use thereof for the treatment of diseases, particularly diseases of the lungs and airways.
Control of the J-Aggregation Phenomenon by Variation of the N-Alkyl-Substituents
Rossi, Umberto De,Moll, Johannes,Spieles, Monika,Bach, Guenther,Daehne, Siegfried,et al.
, p. 203 - 208 (2007/10/02)
Cyanine dyes (1a-d) with the 5,5',6,6'-tetrachloro-1,1'-dialkyl-3,3'-di-(3-carboxypropyl)-benzimidocarbocyanine chromophore differing only in the chain length of their alkyl groups in 1,1'position have been synthesized spectroscopically characterized, and compared with 5,5',6,6'-tetrachloro-1,1'-diethyl-3,3'-di-(4-sulfobutyl)-benzimidocarbocyanine (TDBC).In aqueous solution the dyes form J-aggregates which, depending on the alkyl group chain length, exhibit J-bands differing in spectral position, bandwidth, and in the number of peaks.
