Search Count: 9
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Bace1 In Complex With (S)-5-(3-Chloro-5-(5-(Prop-1-Yn-1-Yl)Pyridin-3-Yl)Thiophen-2-Yl)-2,5-Dimethyl-1,2,4-Thiadiazinan-3-Iminium 1,1-Dioxide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2016-11-09 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 66J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-09
Ligands: 66J
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Bace1 In Complex With 4-(3-(Furan-2-Carboxamido)Phenyl)-1-Methyl-5-Oxo-4-Phenylimidazolidin-2-Iminium
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.83 Å Release Date: 2016-11-09 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: TLA, 66H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-09
Ligands: TLA, 66H
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Bace1 In Complex With (R)-N-(3-(3-Amino-2,5-Dimethyl-1,1-Dioxido-5,6-Dihydro-2H-1,2,4-Thiadiazin-5-Yl)-4-Fluorophenyl)-5-Fluoropicolinamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2016-11-09 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 66F |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-09
Ligands: 66F
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Structure Of Tetragonal Lysozyme In Complex With Iodine Solved By Uwo Students
Organism: Gallus gallus
Method: X-RAY DIFFRACTION Resolution:1.38 Å Release Date: 2015-09-16 Classification: HYDROLASE Ligands: IOD, EDO, ACT |
Organism: Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2015-09-16
Ligands: IOD, EDO, ACT
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Structure Of Tetragonal Lysozyme Solved By Uwo Students
Organism: Gallus gallus
Method: X-RAY DIFFRACTION Resolution:1.22 Å Release Date: 2015-09-16 Classification: HYDROLASE Ligands: EDO, CL |
Organism: Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2015-09-16
Ligands: EDO, CL
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Structure Of Bace In Complex With (S)-4-(3-Chloro-5-(5-(Prop-1-Yn-1-Yl)Pyridin-3-Yl)Thiophen-2-Yl)-1,4-Dimethyl-6-Oxotetrahydropyrimidin-2(1H)-Iminium
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2012-08-08 Classification: Hydrolase/Hydrolase inhibitor Ligands: 0V6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-08-08
Ligands: 0V6
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The Sar Development Of Dihydroimidazoisoquinoline Derivatives As Phosphodiesterase 10A Inhibitors For The Treatment Of Schizophrenia
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2012-03-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 0JP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-14
Ligands: MG, ZN, 0JP
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The Discovery Of Potent, Selectivity, And Orally Bioavailable Pyrozoloquinolines As Pde10 Inhibitors For The Treatment Of Schizophrenia
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2012-01-25 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 0CV, MG, ZN, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-01-25
Ligands: 0CV, MG, ZN, PO4
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Discovery Of Orally Active Pyrazoloquinoline As A Potent Pde10 Inhibitor For The Management Of Schizophrenia
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.28 Å Release Date: 2011-12-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: C1L, MG, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-12-21
Ligands: C1L, MG, ZN