Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry
Reference27 articles.
1. The compounds are commonly called ‘bis(guanylhydrazones)’. Therefore, their established abbreviations contain the letters GBG preceded by an indication of the substituents (e.g., DE for diethyl or EM for ethyl methyl). The term ‘bis-(amidinohydrazone)’ is, however, more appropriate. The Chemical Abstracts' systematic name of MGBG is 2,2′-(1-methyl-1,2-ethanediylidene)bis(hydrazinecarboximidamide), and other congeners are named analogously
2. Methyl glyoxal bis(guanylhydrazone) as a potent inhibitor of mammalian and yeast S-adenosylmethionine decarboxylases
3. Glyoxal bis(guanylhydrazone) as an inhibitor of polyamine biosynthesis in tumour cells
4. Specific inhibition of the enzymic decarboxylation of S-adenosylmethionine by methylglyoxal bis(guanylhydrazone) and related substances
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1. A new class of arylsulfonamide-based 3-acetyl-2-methyl-4-phenylquinolines and in vitro evaluation of their antioxidant, antifungal, and antibacterial activities;Research on Chemical Intermediates;2017-05-05
2. Azine-Hydrazone Tautomerism of Guanylhydrazones: Evidence for the Preference Toward the Azine Tautomer;The Journal of Organic Chemistry;2016-08-24
3. Corrigendum: Aqueous Sulfate Separation by Crystallization of Sulfate-Water Clusters;Angewandte Chemie International Edition;2016-02-02
4. Berichtigung: Aqueous Sulfate Separation by Crystallization of Sulfate-Water Clusters;Angewandte Chemie;2016-02-02
5. On the self-condensation of aminoguanidine leading to 1,1,4,10,10-pentaamino-2,3,5,6,8,9-hexaazadeca-1,3,5,7,9-pentaene (structure elucidation through X-ray powder diffraction);Tetrahedron;2014-10