Amine functionalized trans-cyclooctene derivative for incorporation of the cyclooctene moiety into carboxyl containing compounds or biomolecules via standard coupling techniques (DCC; EDC etc...). Trans-cyclooctenes are useful in strain-promoted copper-free click chemistry cycloaddition reactions with 1; 2; 4; 5-tetrazines. This cyclooctene will react with tetrazine functionalized compounds or biomolecules without the need for a catalyst to result in a stable covalent linkage. The 4+2 inverse electron demand Diels-Alder cycloaddition between trans-cyclooctene and tetrazines is the fastest biologically compatible ligation technology reported and has had many applications in biological labeling and imaging.
1.Mark R Karver, Ralph Weissleder, Scott A Hilderbrand,. (2011-09-29) Synthesis and evaluation of a series of 1,2,4,5-tetrazines for bioorthogonal conjugation.. Bioconjugate chemistry, 22 ((11)):( 2263-2270 ). [PMID:21950520]
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