3JXW
Discovery of 3H-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as Potent, Highly Selective and Orally Bioavailable Pim Kinases Inhibitors
Summary for 3JXW
Entry DOI | 10.2210/pdb3jxw/pdb |
Descriptor | Proto-oncogene serine/threonine-protein kinase Pim-1, 8-[(E)-2-cyclopropylethenyl]-2-[(dimethylamino)methyl][1]benzothieno[3,2-d]pyrimidin-4(3H)-one (2 entities in total) |
Functional Keywords | pim-1, alternative initiation, atp-binding, cell membrane, cytoplasm, kinase, manganese, membrane, metal-binding, nucleotide-binding, nucleus, phosphoprotein, polymorphism, proto-oncogene, serine/threonine-protein kinase, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Isoform 2: Cytoplasm. Isoform 1: Cell membrane: P11309 |
Total number of polymer chains | 1 |
Total formula weight | 34288.94 |
Authors | Stoll, V.S. (deposition date: 2009-09-21, release date: 2009-11-10, Last modification date: 2024-02-21) |
Primary citation | Tao, Z.F.,Hasvold, L.,Leverson, J.,Han, E.,Guan, R.,Johson, E.F.,Stoll, V.S.,Stewart, K.D.,Stamper, G.,Soni, N. Discovery of 3H-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as Potent, Highly Selective and Orally Bioavailable Pim Kinases Inhibitors TO BE PUBLISHED, |
Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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