Search Count: 5
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Crystal Structure Of Human Brd4(1) In Complex With 4-[(2E)-3-(4-Methoxyphenyl)-2-Phenylprop-2-Enoyl]-3,4-Dihydroquinoxalin-2(1H)-One (Compound 19A)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2016-01-13 Classification: PROTEIN BINDING Ligands: Y80 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-01-13
Ligands: Y80
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Crystal Structure Of Human Brd4(1) In Complex With 4-[(5-Phenylpyridin-3-Yl)Carbonyl]-3,4-Dihydroquinoxalin-2(1H)-One (Compound 19D)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.33 Å Release Date: 2016-01-13 Classification: PROTEIN BINDING Ligands: Y81, GOL, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-01-13
Ligands: Y81, GOL, NA
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 3-(1-Phenyl-1H-Pyrazol-5-Yl)-1-(3-(Trifluoromethyl)Phenyl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 3KG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: MG, ZN, 3KG
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 5-Methoxy-3-(1-Phenyl-1H-Pyrazol-5-Yl)-1-(3-(Trifluoromethyl)Phenyl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.68 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 3KB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: ZN, MG, 3KB
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 1-(2-Fluoro-4-(1H-Pyrazol-1-Yl)Phenyl)-5-Methoxy-3-(1-Phenyl-1H-Pyrazol-5-Yl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 3K9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: MG, ZN, 3K9