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5EHO

Rapid Discovery of Pyrido[3,4-d]pyrimidine Inhibitors of Monopolar Spindle kinase 1 (MPS1) Using a Structure-Based Hydridization Approach

Summary for 5EHO
Entry DOI10.2210/pdb5eho/pdb
Related5EH0
DescriptorDual specificity protein kinase TTK, ~{N}8-cyclohexyl-~{N}2-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]pyrido[3,4-d]pyrimidine-2,8-diamine, DIMETHYL SULFOXIDE, ... (4 entities in total)
Functional Keywordsspindle assembly checkpoint (sac), oncology target pyrido[3, 4-d]pyrimidine based inhibitors selective against mps1, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight36622.91
Authors
Primary citationInnocenti, P.,Woodward, H.L.,Solanki, S.,Naud, N.,Westwood, I.M.,Cronin, N.,Hayes, A.,Roberts, J.,Henley, A.T.,Baker, R.,Faisal, A.,Mak, G.,Box, G.,Valenti, M.,De Haven Brandon, A.,O'Fee, L.,Saville, J.,Schmitt, J.,Burke, R.,van Montfort, R.L.M.,Raymaud, F.I.,Eccles, S.A.,Linardopoulos, S.,Blagg, J.,Hoelder, S.
Rapid Discovery of Pyrido[3,4-d]pyrimidine Inhibitors of Monopolar Spindle kinase 1 (MPS1) Using a Structure-Based Hydridization Approach
To Be Published,
Experimental method
X-RAY DIFFRACTION (2.18 Å)
Structure validation

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PDB entries from 2024-10-30

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