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5WEV

Identification of an imidazopyridine scaffold to generate potent and selective TYK2 inhibitors that demonstrate activity in an in vivo psoriasis model

Summary for 5WEV
Entry DOI10.2210/pdb5wev/pdb
DescriptorTyrosine-protein kinase JAK2, N-[2-(2,6-dichlorophenyl)-1H-imidazo[4,5-c]pyridin-4-yl]cyclopropanecarboxamide (3 entities in total)
Functional Keywordsjak2, kinase, 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 weight37722.54
Authors
Ultsch, M.H.,Magnuson, S. (deposition date: 2017-07-10, release date: 2017-09-06, Last modification date: 2023-11-15)
Primary citationLiang, J.,Van Abbema, A.,Balazs, M.,Barrett, K.,Berezhkovsky, L.,Blair, W.S.,Chang, C.,Delarosa, D.,DeVoss, J.,Driscoll, J.,Eigenbrot, C.,Goodacre, S.,Ghilardi, N.,MacLeod, C.,Johnson, A.,Bir Kohli, P.,Lai, Y.,Lin, Z.,Mantik, P.,Menghrajani, K.,Nguyen, H.,Peng, I.,Sambrone, A.,Shia, S.,Smith, J.,Sohn, S.,Tsui, V.,Ultsch, M.,Williams, K.,Wu, L.C.,Yang, W.,Zhang, B.,Magnuson, S.
Identification of an imidazopyridine scaffold to generate potent and selective TYK2 inhibitors that demonstrate activity in an in vivo psoriasis model.
Bioorg. Med. Chem. Lett., 27:4370-4376, 2017
Cited by
PubMed: 28830649
DOI: 10.1016/j.bmcl.2017.08.022
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.854 Å)
Structure validation

222036

数据于2024-07-03公开中

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