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7QPM
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BU of 7qpm by Molmil
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
分子名称: 5,7-dimethyl-2-[(1-methyl-4-phenyl-imidazol-2-yl)sulfanylmethyl]imidazo[1,2-a]pyrimidine, MAGNESIUM ION, ZINC ION, ...
著者Leonard, P.M, Langgard, M.
登録日2022-01-05
公開日2023-04-19
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published
7QPF
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BU of 7qpf by Molmil
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
分子名称: 2-(1~{H}-benzimidazol-2-ylsulfanylmethyl)-3-bromanyl-5,7-dimethyl-imidazo[1,2-a]pyrimidine, MAGNESIUM ION, ZINC ION, ...
著者Leonard, P.M, Langgard, M.
登録日2022-01-04
公開日2023-04-19
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published
7QQ4
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BU of 7qq4 by Molmil
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
分子名称: 5,8-dimethyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyrazine, MAGNESIUM ION, ZINC ION, ...
著者Leonard, P.M, Langgard, M.
登録日2022-01-06
公開日2023-04-19
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.45 Å)
主引用文献Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published
7QPQ
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BU of 7qpq by Molmil
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
分子名称: 2-[(1-methyl-4-phenyl-imidazol-2-yl)methylsulfanyl]-[1,2,4]triazolo[1,5-a]pyridine, MAGNESIUM ION, ZINC ION, ...
著者Leonard, P.M, Langgard, M.
登録日2022-01-05
公開日2023-04-19
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published
7QPV
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BU of 7qpv by Molmil
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
分子名称: 8-methyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyridine, MAGNESIUM ION, ZINC ION, ...
著者Leonard, P.M, Langgard, M.
登録日2022-01-05
公開日2023-04-19
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published
1R3G
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BU of 1r3g by Molmil
1.16A X-ray structure of the synthetic DNA fragment with the incorporated 2'-O-[(2-Guanidinium)ethyl]-5-methyluridine residues
分子名称: 5'-D(*GP*CP*GP*TP*AP*(GMU)P*AP*CP*GP*C)-3'), MAGNESIUM ION
著者Prakash, T.P, Puschl, A, Lesnik, E, Tereshko, V, Egli, M, Manoharan, M.
登録日2003-10-01
公開日2003-10-21
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.16 Å)
主引用文献2'-O-[2-(Guanidinium)ethyl]-Modified Oligonucleotides: Stabilizing Effect on Duplex and Triplex Structures.
Org.Lett., 6, 2004

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件を2024-04-24に公開中

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