Bioorthogonal Removal of 3-Isocyanopropyl Groups Enables the Controlled Release of Fluorophores and Drugs in Vivo-Reference-Cited by-同舟云学术

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Bioorthogonal Removal of 3-Isocyanopropyl Groups Enables the Controlled Release of Fluorophores and Drugs in Vivo

Published:2018-06-21 Issue:27 Volume:140 Page:8410-8414
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Tu Julian¹^ORCID,Xu Minghao¹^ORCID,Parvez Saba²,Peterson Randall T.²,Franzini Raphael M.¹^ORCID

Affiliation:

1. Department of Medicinal Chemistry, College of Pharmacy, University of Utah, 30 S 2000 E, Salt Lake City, Utah 84112, United States

2. Department of Pharmacology and Toxicology, College of Pharmacy, University of Utah, 30 S 2000 E, Salt Lake City, Utah 84112, United States

Funder

University of Utah

Huntsman Cancer Institute

Utah Science Technology and Research

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.8b05093

Reference48 articles.

1. Design strategies for bioorthogonal smart probes

2. Development and application of bond cleavage reactions in bioorthogonal chemistry

3. Imaging of mRNA in Live Cells Using Nucleic Acid-Templated Reduction of Azidorhodamine Probes

4. Efficient Nucleic Acid Detection by Templated Reductive Quencher Release

5. Bioorthogonal Tetrazine-Mediated Transfer Reactions Facilitate Reaction Turnover in Nucleic Acid-Templated Detection of MicroRNA

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