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6Q6F
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Crystal structure of IDH1 R132H in complex with HMS101
分子名称: (2~{R})-2-[2-[(3~{R})-3-(4-fluorophenyl)pyrrolidin-1-yl]ethyl]-1,4-dimethyl-piperazine, Isocitrate dehydrogenase [NADP] cytoplasmic
著者Chaturvedi, A, Goparaju, R, Gupta, C, Kluenemann, T, Araujo Cruz, M.M, Kloos, A, Goerlich, K, Schottmann, R, Struys, E.A, Ganser, A, Preller, M, Heuser, M.
登録日2018-12-10
公開日2019-10-16
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献In vivo efficacy of mutant IDH1 inhibitor HMS-101 and structural resolution of distinct binding site.
Leukemia, 34, 2020

219515

件を2024-05-08に公開中

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