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Cited by 283

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

d -Amino Acids Boost the Selectivity and Confer Supramolecular Hydrogels of a Nonsteroidal Anti-Inflammatory Drug (NSAID)

Open access
Li, Jiayang, Kuang, Yi, Gao, Yuan, Du, Xuewen, Shi, Junfeng, Xu, Bing·2013·Journal of the American Chemical Society

Abstract

As systemically used therapeutics for treating acute or chronic pains or inflammations, nonsteroidal anti-inflammatory drugs (NSAIDs) also associate with the adverse gastrointestinal and renal effects and cardiovascular risks. Thus, it is beneficial to develop topical gels that selectively inhibit cyclooxygenase-2 (COX-2) for the management of local inflammation. In this work, we demonstrate that the covalent conjugation of d-amino acids to naproxen (i.e., a NSAID) not only affords supramolecular hydrogelators for the topical gels but also unexpectedly and significantly elevates the selectivity toward COX-2 about 20× at little expense of the activity of naproxen. This work illustrates a previously unexplored approach that employs d-amino acids for the development of functional molecules that have dual or multiple roles and exceptional biostability, which offers a new class of molecular hydrogels of therapeutic agents.

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Crossref · 10.1021/ja310019x

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Metadata

Authors
Li, J., Kuang, Y., Gao, Y., Du, X., Shi, J., & Xu, B.
Venue
Journal of the American Chemical Society
Published
2012-11-14
Volume
135
Issue
2
Pages
542-545
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2024829972
Cited by
283
References
5
FWCI
11.66
Type
journal article
Language
en
Open access
green

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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