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3VAP
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BU of 3vap by Molmil
Synthesis and SAR Studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off target kinase selectivity
分子名称: 3-(1-{2-[(3-fluoropyridinium-4-yl)amino]-2-oxoethyl}-1H-pyrazol-4-yl)-6-methyl-8-[(3-{[(1R,3R)-3-methylpiperidinium-1-yl]methyl}-1,2-thiazol-5-yl)amino]imidazo[1,2-a]pyrazin-1-ium, Aurora kinase A
著者Voss, M.E, Rainka, M.P, Fleming, M, Peterson, L.H, Belanger, D.B, Siddiqui, M.A, Hruza, A, Voigt, J, Basso, A.D, Gray, K.
登録日2011-12-29
公開日2012-05-02
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (2.66 Å)
主引用文献Synthesis and SAR studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off-target kinase selectivity.
Bioorg.Med.Chem.Lett., 22, 2012
4HV6
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BU of 4hv6 by Molmil
Structure of MNTR H77A mutant in apo- and mn-bound forms
分子名称: MAGNESIUM ION, MANGANESE (II) ION, Transcriptional regulator MntR
著者Glasfeld, A, Grauer-Gray, K, McGuire, A.
登録日2012-11-05
公開日2012-11-21
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Roles of the A and C sites in the manganese-specific activation of MntR.
Biochemistry, 52, 2013
3NRM
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BU of 3nrm by Molmil
Imidazo[1,2-a]pyrazine-based Aurora Kinase Inhibitors
分子名称: N-(3-methylisothiazol-5-yl)-3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-amine, Serine/threonine-protein kinase 6
著者Hruza, A.
登録日2010-06-30
公開日2010-08-18
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (3.05 Å)
主引用文献Discovery of imidazo[1,2-a]pyrazine-based Aurora kinase inhibitors.
Bioorg.Med.Chem.Lett., 20, 2010
3NSZ
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BU of 3nsz by Molmil
Human CK2 catalytic domain in complex with AMPPN
分子名称: Casein kinase II subunit alpha, GLYCEROL, MAGNESIUM ION, ...
著者Ferguson, A.D.
登録日2010-07-02
公開日2010-12-15
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (1.3 Å)
主引用文献Structural basis of CX-4945 binding to human protein kinase CK2.
Febs Lett., 585, 2011
3MYG
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BU of 3myg by Molmil
Aurora A Kinase complexed with SCH 1473759
分子名称: 2-{ethyl[(5-{[6-methyl-3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino}isothiazol-3-yl)methyl]amino}-2-methylpropan-1-ol, Serine/threonine-protein kinase 6, TETRAETHYLENE GLYCOL
著者Hruza, A, Prosis, W, Ramanathan, L.
登録日2010-05-10
公開日2010-07-21
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Discovery of a Potent, Injectable Inhibitor of Aurora Kinases Based on the Imidazo-[1,2-a]-Pyrazine Core.
ACS Med Chem Lett, 1, 2010
3NGA
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BU of 3nga by Molmil
Human CK2 catalytic domain in complex with CX-4945
分子名称: 5-[(3-chlorophenyl)amino]benzo[c][2,6]naphthyridine-8-carboxylic acid, Casein kinase II subunit alpha, SULFATE ION
著者Ferguson, A.D.
登録日2010-06-11
公開日2010-12-15
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.71 Å)
主引用文献Structural basis of CX-4945 binding to human protein kinase CK2.
Febs Lett., 585, 2011

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件を2024-07-17に公開中

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