タイトル | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate |
---|
ジャーナル・号・ページ | To Be Published |
---|
掲載日 | 2022年1月4日 (構造データの登録日) |
---|
著者 | Kehler, J. / Kilburn, J.P. / Langgard, M. / Christoffersen, C.T. / Ritzen, A. / Marigo, M. / Jessing, M. / Bundgaard, C. / Puschl, A. / Feigin, K. / Nielsen, J. |
---|
リンク | PubMedで検索 |
---|
手法 | X線回折 |
---|
解像度 | 1.7 - 2.45 Å |
---|
構造データ | PDB-7qpf: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate 手法: X-RAY DIFFRACTION / 解像度: 1.7 Å PDB-7qpm: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-7qpq: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-7qpv: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate 手法: X-RAY DIFFRACTION / 解像度: 2.3 Å PDB-7qq4: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate 手法: X-RAY DIFFRACTION / 解像度: 2.45 Å |
---|
化合物 | ChemComp-EFJ: 2-(1~{H}-benzimidazol-2-ylsulfanylmethyl)-3-bromanyl-5,7-dimethyl-imidazo[1,2-a]pyrimidine
ChemComp-EEI: 5,7-dimethyl-2-[(1-methyl-4-phenyl-imidazol-2-yl)sulfanylmethyl]imidazo[1,2-a]pyrimidine
ChemComp-EIH: 2-[(1-methyl-4-phenyl-imidazol-2-yl)methylsulfanyl]-[1,2,4]triazolo[1,5-a]pyridine
ChemComp-EHI: 8-methyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyridine
ChemComp-EIK: 5,8-dimethyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyrazine
|
---|
由来 | - homo sapiens (ヒト)
|
---|
キーワード | HYDROLASE / Phosphodiesterase / PDE / PDE10A / schizophrenia / basal ganglia disorders |
---|