New Electrophiles and Strategies for Mechanism-Based and Targeted Covalent Inhibitor Design
Covalent inhibitors are experiencing a growing resurgence in drug design and are an increasingly useful tool in molecular biology. The ability to attach inhibitors to their targets by a covalent linkage offers pharmacodynamic and pharmacokinetic advantages, but this can also be a liability if undesired off-target reactions are not mitigated. The discovery of new electrophilic groups that react selectively with specific amino acid residues is therefore highly desirable in the design of targeted covalent inhibitors (TCIs). Additionally, the ability to control the reactivity through exploitation of the target enzyme's machinery, as in mechanism-based inhibitors (MBIs), greatly benefits from the discovery of new strategies. This Perspective showcases recent advances in electrophile development and their application in TCIs and MBIs, exhibiting high selectivity for their targets.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2019 |
---|---|
Erschienen: |
2019 |
Enthalten in: |
Zur Gesamtaufnahme - volume:58 |
---|---|
Enthalten in: |
Biochemistry - 58(2019), 52 vom: 31. Dez., Seite 5234-5244 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Ray, Sneha [VerfasserIn] |
---|
Links: |
---|
Themen: |
Enzyme Inhibitors |
---|
Anmerkungen: |
Date Completed 22.06.2020 Date Revised 22.06.2020 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1021/acs.biochem.9b00293 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM296114006 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM296114006 | ||
003 | DE-627 | ||
005 | 20231225085133.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2019 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/acs.biochem.9b00293 |2 doi | |
028 | 5 | 2 | |a pubmed24n0987.xml |
035 | |a (DE-627)NLM296114006 | ||
035 | |a (NLM)30990686 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Ray, Sneha |e verfasserin |4 aut | |
245 | 1 | 0 | |a New Electrophiles and Strategies for Mechanism-Based and Targeted Covalent Inhibitor Design |
264 | 1 | |c 2019 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 22.06.2020 | ||
500 | |a Date Revised 22.06.2020 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Covalent inhibitors are experiencing a growing resurgence in drug design and are an increasingly useful tool in molecular biology. The ability to attach inhibitors to their targets by a covalent linkage offers pharmacodynamic and pharmacokinetic advantages, but this can also be a liability if undesired off-target reactions are not mitigated. The discovery of new electrophilic groups that react selectively with specific amino acid residues is therefore highly desirable in the design of targeted covalent inhibitors (TCIs). Additionally, the ability to control the reactivity through exploitation of the target enzyme's machinery, as in mechanism-based inhibitors (MBIs), greatly benefits from the discovery of new strategies. This Perspective showcases recent advances in electrophile development and their application in TCIs and MBIs, exhibiting high selectivity for their targets | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, U.S. Gov't, Non-P.H.S. | |
650 | 4 | |a Review | |
650 | 7 | |a Enzyme Inhibitors |2 NLM | |
700 | 1 | |a Murkin, Andrew S |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Biochemistry |d 1962 |g 58(2019), 52 vom: 31. Dez., Seite 5234-5244 |w (DE-627)NLM000000469 |x 1520-4995 |7 nnns |
773 | 1 | 8 | |g volume:58 |g year:2019 |g number:52 |g day:31 |g month:12 |g pages:5234-5244 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/acs.biochem.9b00293 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 58 |j 2019 |e 52 |b 31 |c 12 |h 5234-5244 |