Probing Secondary Carbohydrate-Protein Interactions with Highly Dense Cyclodextrin-Centered Heteroglycoclusters: The Heterocluster Effect was written by Gomez-Garcia, Marta;Benito, Juan M.;Rodriguez-Lucena, David;Yu, Jian-Xin;Chmurski, Kazimierz;Mellet, Carmen Ortiz;Gallego, Ricardo Gutierrez;Maestre, Alfredo;Defaye, Jacques;Fernandez, Jose M. Garcia. And the article was included in Journal of the American Chemical Society in 2005.Category: bromides-buliding-blocks This article mentions the following:
Comparison of the lectin-binding properties for highly dense β-cyclodextrin-centered homo- and heteroglycoclusters with defined architecture provides evidence for the existence of strong synergic effects (heterocluster effect) on carbohydrate-protein recognition events. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1Category: bromides-buliding-blocks).
Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Category: bromides-buliding-blocks
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary