Trimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology
被引:109
作者:
Levine, Michael N.
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机构:
Univ Wisconsin, Dept Biochem, Madison, WI 53706 USAUniv Wisconsin, Dept Biochem, Madison, WI 53706 USA
Levine, Michael N.
[1
]
Raines, Ronald T.
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h-index: 0
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Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
Univ Wisconsin, Dept Chem, Madison, WI 53706 USAUniv Wisconsin, Dept Biochem, Madison, WI 53706 USA
Raines, Ronald T.
[1
,2
]
机构:
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
The trimethyl lock is an o-hydroxydihydrocinnamic acid derivative in which unfavorable steric interactions between three pendant methyl groups encourage lactonization to form a hydrocoumarin. This reaction is extremely rapid, even when the electrophile is an amide and the leaving group is an amino group of a small-molecule drug, fluorophore, peptide, or nucleic acid. O-Acylation of the phenolic hydroxyl group prevents reaction, providing a trigger for the reaction. Thus, the release of an amino group from an amide can be coupled to the hydrolysis of a designated ester (or to another chemical reaction that regenerates the hydroxyl group). Trimethyl lock conjugates are easy to synthesize, making the trimethyl lock a highly versatile module for chemical biology and related fields.