Search Count: 3
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Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 16J (6-(4-Methoxybenzyl)-9-((Tetrahydro-2H-Pyran-4-Yl)Methyl)-8,9,10,11-Tetrahydropyrido[4',3':4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.82 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HM
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Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 3 (6-(4-Chlorobenzyl)-8,9,10,11-Tetrahydrobenzo[4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HP
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Crystal Structure Of Human Pde10A In Complex With Inhibitor 16D
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2017-04-26 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 8Q7, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: 8Q7, ZN, MG