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5TQ8

Design and Synthesis of a pan-JAK Kinase Inhibitor Clinical Candidate (PF-06263276) Suitable for Inhaled and Topical Delivery for the Treatment of Inflammatory Diseases of the Lungs and Skin

Summary for 5TQ8
Entry DOI10.2210/pdb5tq8/pdb
Related5TQ3 5TQ4 5TQ5 5TQ6 5TQ7 5TQ8
DescriptorTyrosine-protein kinase JAK2, {2-[6-(2-ethyl-5-fluoro-4-hydroxyphenyl)-2H-indazol-3-yl]-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridin-5-yl}[5-(piperidin-1-yl)pyrazin-2-yl]methanone (3 entities in total)
Functional Keywordskinase, inflammation, jak inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationEndomembrane system ; Peripheral membrane protein : O60674
Total number of polymer chains1
Total formula weight35440.36
Authors
Chrencik, J.,Jones, P. (deposition date: 2016-10-23, release date: 2017-01-11, Last modification date: 2023-10-04)
Primary citationJones, P.,Storer, R.I.,Sabnis, Y.A.,Wakenhut, F.M.,Whitlock, G.A.,England, K.S.,Mukaiyama, T.,Dehnhardt, C.M.,Coe, J.W.,Kortum, S.W.,Chrencik, J.E.,Brown, D.G.,Jones, R.M.,Murphy, J.R.,Yeoh, T.,Morgan, P.,Kilty, I.
Design and Synthesis of a Pan-Janus Kinase Inhibitor Clinical Candidate (PF-06263276) Suitable for Inhaled and Topical Delivery for the Treatment of Inflammatory Diseases of the Lungs and Skin.
J. Med. Chem., 60:767-786, 2017
Cited by
PubMed: 27983835
DOI: 10.1021/acs.jmedchem.6b01634
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.59 Å)
Structure validation

218196

數據於2024-04-10公開中

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