Campbell McInnes - Concepedia

Author

Campbell McInnes

Cyclacel Pharmaceuticals (United Kingdom)

Also Known As

C. MCINNES, C. McInnes, Campbell McInnes, Campbell Mcinnes, M.D. Walkinshaw

Publications

901

Citations

H-Index

Concepts

All Affiliations

Cyclacel Pharmaceuticals (United Kingdom)University of Edinburgh

About

Campbell McInnes is an author at Cyclacel Pharmaceuticals (United Kingdom) specializing in medicine, natural sciences, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	594
2	Natural Sciences	6	6	453
3	Biochemistry	4	4	285
4	Biomolecular Engineering	2	2	156
5	Engineering	1	1	51

Campbell McInnes

Publications

874

Citations

H-Index

Page 1

	Year	Citations
2-Anilino-4-(thiazol-5-yl)pyrimidine CDK Inhibitors: Synthesis, SAR Analysis, X-ray Crystallography, and Biological Activity Shudong Wang, Christopher Meades, Gavin Wood, Journal of Medicinal Chemistry X-ray CrystallographyMolecular DockingMedicinal ChemistryVirtual ScreeningPyrimidine Cdk Inhibitors	2004	151
Structure of Free MDM2 N-terminal Domain Reveals Conformational Adjustments that Accompany p53-binding Stanislava Uhrı́nová, Helen Powers, K. Watt, Journal of Molecular Biology Structural BioinformaticsMolecular BiologyStructural BiologyProtein NmrMolecular Basis	2005	141
Structural and biochemical studies of human proliferating cell nuclear antigen complexes provide a rationale for cyclin association and inhibitor design George Kontopidis, Su‐Ying Wu, Daniella Zheleva, Proceedings of the National Academy of Sciences	2005	130
Discovery of a Novel Family of CDK Inhibitors with the Program LIDAEUS S. Y. Wu, I.W. McNae, George Kontopidis, Structure Cdk InhibitorsMedicinal ChemistryMedicineProgram LidaeusNatural Sciences	2003	105
Development of the Structural Basis for Antimicrobial and Hemolytic Activities of Peptides Based on Gramicidin S and Design of Novel Analogs Using NMR Spectroscopy Campbell McInnes, Leslie H. Kondejewski, Robert S. Hodges, Journal of Biological Chemistry	2000	67
Insights into Cyclin Groove Recognition George Kontopidis, Martin J. I. Andrews, Campbell McInnes, Structure Natural SciencesSignal RecognitionMolecular BiologyCyclin Groove RecognitionStructural Biology	2003	63
Highly potent p21<sup>WAF1</sup>‐derived peptide inhibitors of CDK‐mediated pRb phosphorylation: Delineation and structural insight into their interactions with cyclin A Daniella Zheleva, Campbell McInnes, A.‐L. Gavine, Journal of Peptide Research Potency EnhancementRetinoblastoma ProteinMolecular BiologyPeptide ScienceHakrrlif Peptide	2002	60
Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes Martin J. I. Andrews, Campbell McInnes, George Kontopidis, Organic & Biomolecular Chemistry Bioorganic ChemistryMolecular BiologyPotency IncreaseChemical BiologyMedicinal Chemistry	2004	56
Design of a versatile linker for solid phase peptide synthesis: Synthesis of C-terminal primary/seconary amides and hydrazides R. Ramage, S.L. Irving, Campbell McInnes Tetrahedron Letters EngineeringPeptide EngineeringPeptide LibraryPeptide SynthesisOrganic Chemistry	1993	51
Design, Synthesis, and Evaluation of 2-Methyl- and 2-Amino-<i>N</i>-aryl-4,5-dihydrothiazolo[4,5-<i>h</i>]quinazolin-8-amines as Ring-Constrained 2-Anilino-4-(thiazol-5-yl)pyrimidine Cyclin-Dependent Kinase Inhibitors Neil A. McIntyre, Campbell McInnes, Gary Griffiths, Journal of Medicinal Chemistry	2010	32

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