Trimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology

被引:109
作者
Levine, Michael N. [1 ]
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
关键词
HYDROXY AMIDE LACTONIZATION; INTRAMOLECULAR CONJUGATE ADDITION; STEREOPOPULATION-CONTROL; ALKALINE-PHOSPHATASE; PEPTIDE-BOND; DELIVERY SYSTEMS; LATENT FLUOROPHORE; RATE ENHANCEMENT; ANTITUMOR AGENT; AMINE PRODRUGS;
D O I
10.1039/c2sc20536j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
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页码:2412 / 2420
页数:9
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