Search Count: 4
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Synthesis And Biological Evaluation Of Novel Selective Androgen Receptor Modulators (Sarms). Part Ii: Optimization Of 4-(Pyrrolidin-1-Yl)Benzonitrile Derivatives
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.71 Å Release Date: 2017-04-26 Classification: HORMONE RECEPTOR Ligands: GOL, 77U |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: GOL, 77U
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Synthesis And Biological Evaluation Of Novel Selective Androgen Receptor Modulators (Sarms). Part Ii: Optimization Of 4-(Pyrrolidin-1-Yl)Benzonitrile Derivatives
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2017-04-26 Classification: HORMONE RECEPTOR Ligands: GOL, 77T |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: GOL, 77T
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Crystal Structure Of The Catalytic Domain Of Human Pde10A Complexed With N-(4-((5-Methyl-5H-Pyrrolo[3,2-D]Pyrimidin-4-Yl)Oxy)Phenyl)-1H-Benzimidazol-2-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2016-06-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 6DT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-06-29
Ligands: MG, ZN, 6DT
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Crystal Structure Of The Catalytic Domain Of Human Pde10A Complexed With 1-(Cyclopropylmethyl)-5-(2-(2,3-Dihydro-1H-Imidazo[1,2-A]Benzimidazol-1-Yl)Ethoxy)-3-(1-Phenyl-1H-Pyrazol-5-Yl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2016-06-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 6DW |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-06-29
Ligands: MG, ZN, 6DW