Erratum: Selective inhibitors of histone methyltransferase DOT1L: Design, synthesis, and crystallographic studies (Journal of the American Chemical Society (2011) 133 (16746-16749) DOI: 10.1021/ja206312b);Selective inhibitors of histone methyltransferase DOT1L: Design, synthesis, and crystallographic studies

Journal of the American Chemical Society

Volumn 133, Issue 42, 2011, Pages 16746-16749

  Yao, Yuan ^a   Chen, Pinhong ^a   Diao, Jiasheng ^a   Cheng, Gang ^a   Deng, Lisheng ^a   Anglin, Justin L ^a   Prasad, B V Venkataram ^a   Song, Yongcheng ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; HYDROPHOBICITY;

BIOLOGICAL FUNCTIONS; CELL DIFFERENTIATION; CRYSTALLOGRAPHIC STUDIES; HISTONE METHYLTRANSFERASE; HISTONE METHYLTRANSFERASES; HYDROPHOBIC CAVITIES; SELECTIVE INHIBITORS; X RAY CRYSTAL STRUCTURES;

CRYSTAL STRUCTURE;

ANTILEUKEMIC AGENT; DOT1L HISTONE METHYLTRANSFERASE; DOT1L HISTONE METHYLTRANSFERASE INHIBITOR; HISTONE LYSINE METHYLTRANSFERASE; HISTONE METHYLTRANSFERASE; METHYLTRANSFERASE INHIBITOR; PROTEIN ARGININE METHYLTRANSFERASE; UNCLASSIFIED DRUG;

ARTICLE; CELL DIFFERENTIATION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; HUMAN; HYDROGEN BOND; HYDROPHOBICITY; IC 50; LEUKEMIA; NONHUMAN; X RAY CRYSTALLOGRAPHY;

EID: 80055019988     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja309785w     Document Type: Erratum

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