dc.contributor.author |
Denny, William A |
|
dc.coverage.spatial |
Netherlands |
|
dc.date.accessioned |
2022-06-12T23:04:25Z |
|
dc.date.available |
2022-06-12T23:04:25Z |
|
dc.date.issued |
2022-02-15 |
|
dc.identifier.citation |
(2022). Current Cancer Drug Targets, 22(3), 209-220. |
|
dc.identifier.issn |
1568-0096 |
|
dc.identifier.uri |
https://hdl.handle.net/2292/59738 |
|
dc.description.abstract |
The p38 MAP kinases are a sub-family of the broad group of mitogen-activated serine-threonine protein kinases. The best-characterised, most widely expressed, and most targeted by drugs is p38α MAP kinase. This review briefly summarises the place of p38α MAP kinase in cellular signalling and discusses the structures and activity profiles of representative examples of the major classes of inhibitors and activators (both synthetic compounds and natural products) of this enzyme. Primary screening was primarily direct in vitro inhibition of isolated p38α enzyme. |
|
dc.format.medium |
Print-Electronic |
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dc.language |
eng |
|
dc.publisher |
Bentham Science Publishers Ltd. |
|
dc.relation.ispartofseries |
Current cancer drug targets |
|
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
|
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
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dc.subject |
Kinase |
|
dc.subject |
cancer |
|
dc.subject |
inflammation |
|
dc.subject |
inhibitors |
|
dc.subject |
p38MAPK |
|
dc.subject |
review |
|
dc.subject |
2.1 Biological and endogenous factors |
|
dc.subject |
5.1 Pharmaceuticals |
|
dc.subject |
0304 Medicinal and Biomolecular Chemistry |
|
dc.subject |
1112 Oncology and Carcinogenesis |
|
dc.subject |
1115 Pharmacology and Pharmaceutical Sciences |
|
dc.title |
Inhibitors and Activators of the p38 Mitogen- Activated MAP Kinase (MAPK) Family as Drugs to Treat Cancer and Inflammation. |
|
dc.type |
Journal Article |
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dc.identifier.doi |
10.2174/1568009622666220215142837 |
|
pubs.issue |
3 |
|
pubs.begin-page |
209 |
|
pubs.volume |
22 |
|
dc.date.updated |
2022-05-19T23:29:00Z |
|
dc.rights.holder |
Copyright: The author |
en |
dc.identifier.pmid |
35168519 (pubmed) |
|
pubs.author-url |
https://www.ncbi.nlm.nih.gov/pubmed/35168519 |
|
pubs.end-page |
220 |
|
pubs.publication-status |
Published |
|
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
IM |
|
pubs.subtype |
Journal Article |
|
pubs.elements-id |
883324 |
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pubs.org-id |
Medical and Health Sciences |
|
pubs.org-id |
Science |
|
pubs.org-id |
Science Research |
|
pubs.org-id |
Medical Sciences |
|
pubs.org-id |
Auckland Cancer Research |
|
pubs.org-id |
Maurice Wilkins Centre (2010-2014) |
|
dc.identifier.eissn |
1873-5576 |
|
dc.identifier.pii |
CCDT-EPUB-120903 |
|
pubs.record-created-at-source-date |
2022-05-20 |
|