Edward G. McIver

发表

Antagonists of GPR35 Display High Species Ortholog Selectivity and Varying Modes of Action

G. Milligan, S. Nicklin, A. Mackenzie, 2012, Journal of Pharmacology and Experimental Therapeutics.

Edinburgh Research Explorer TBK1 Kinase Addiction in Lung Cancer Cells Is Mediated via Autophagy of Tax1bp1/Ndp52 and Non-Canonical NF-kappa B Signalling

S. Wilkinson, Alice C Newman, Edward G. McIver, 2017 .

An improved Williamson etherification of hindered alcohols promoted by 15-crown-5 and sodium hydride

H. C. Aspinall, N. Greeves, Peter M. Smith, 1997 .

The role of TBK1 and IKKε in the expression and activation of Pellino 1.

P. Cohen, J. Lescar, R. Gourlay, 2011, The Biochemical journal.

Vilsmeier methodology for the synthesis of 3-(2-N-phthaloylacyl)indole derivatives, and its application to the synthesis of the GCDEF rings of diazonamide

P. Magnus, Edward G. McIver, J. D. Kreisberg, 2001 .

Synthesis of the dichlorobisoxazole-indole portion of the antitumor agent diazonamide by a putative biogenetic strategy

P. Magnus, Edward G. McIver, 2000 .

Synthesis of the 4-arylindole portion of the antitumor agent diazonamide and related studies

P. Magnus, Fiona Chan, Edward G. McIver, 2000 .

YTTERBIUM TRIFLATE CATALYSED ALLYLATION OF ALDEHYDES : AN UNUSUAL BENZOIC ACID INDUCED ACCELERATION

H. C. Aspinall, N. Greeves, Edward G. McIver, 1998 .

The search for novel TRPV1-antagonists: from carboxamides to benzimidazoles and indazolones.

S. Boyce, G. Mason, S. Fletcher, 2006, Bioorganic & medicinal chemistry letters.

Modular chiral polyether podands and their lanthanide complexes

H. C. Aspinall, N. Greeves, Edward G. McIver, 2003 .

ACTH Antagonists

A. Clark, Li Chan, J. Jerman, 2016, Front. Endocrinol..

Novel cross-talk within the IKK family controls innate immunity.

P. Cohen, J. Madwed, M. Peggie, 2011, The Biochemical journal.

High-Throughput Identification and Characterization of Novel, Species-selective GPR35 Agonists

Graeme Milligan, G. Milligan, A. Mackenzie, 2013, The Journal of Pharmacology and Experimental Therapeutics.

TBK1 Kinase Addiction in Lung Cancer Cells Is Mediated via Autophagy of Tax1bp1/Ndp52 and Non-Canonical NF-κB Signalling

S. Wilkinson, Edward G. McIver, Caroline L. Scholefield, 2012, PloS one.

Phosphorylation of CRTC3 by the salt-inducible kinases controls the interconversion of classically activated and regulatory macrophages

Patrick G. A. Pedrioli, Nathanael S. Gray, P. Cohen, 2012, Proceedings of the National Academy of Sciences.

Discovery of potent azaindazole leucine-rich repeat kinase 2 (LRRK2) inhibitors possessing a key intramolecular hydrogen bond - Part 2.

A. Beresford, A. Medhurst, Xingrong Liu, 2019, Bioorganic & medicinal chemistry letters.

The search for novel TRPV1-antagonists: from carboxamides to benzimidazoles and indazolones.

S. Boyce, G. Mason, S. Fletcher, 2006, Bioorganic & medicinal chemistry letters.

Identification of a novel specific small-molecule melanocortin-2-receptor antagonist

J. Jerman, A. Clark, Debra L. Taylor, 2022, Endocrine connections.

Evaluating the druggability of TrmD, a potential antibacterial target, through design and microbiological profiling of a series of potent TrmD inhibitors.

R. Newman, P. Coombs, K. Ansell, 2023, Bioorganic & medicinal chemistry letters.

Discovery of potent and selective 5-azaindazole inhibitors of leucine-rich repeat kinase 2 (LRRK2) - Part 1.

D. Alessi, S. Lewis, Debra L. Taylor, 2019, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of a novel series of pyrimidines as potent inhibitors of TBK1/IKKε kinases.

P. Cohen, J. Arthur, J. Bryans, 2012, Bioorganic & medicinal chemistry letters.

ACTH Antagonists

J. Newell-Price, A. Clark, Li Chan, 2016, Front. Endocrinol..