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7OE9

C-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH rac-N5-((1R,5S)-3-oxabicyclo[3.1.0]hexan-6-yl)-N7,3-dimethyl-3-phenyl-2,3-dihydrobenzofuran-5,7-dicarboxamide

Summary for 7OE9
Entry DOI10.2210/pdb7oe9/pdb
Related7OE8
DescriptorBromodomain-containing protein 2, (3S)-N7,3-dimethyl-N5-[(1R,5S)-3-oxabicyclo[3.1.0]hexan-6-yl]-3-phenyl-2H-1-benzofuran-5,7-dicarboxamide, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordsinhibitor, bromodomain, nuclear protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight13949.05
Authors
Chung, C. (deposition date: 2021-05-02, release date: 2021-07-28, Last modification date: 2021-08-25)
Primary citationLucas, S.C.C.,Atkinson, S.J.,Chung, C.W.,Davis, R.,Gordon, L.,Grandi, P.,Gray, J.J.R.,Grimes, T.,Phillipou, A.,Preston, A.G.,Prinjha, R.K.,Rioja, I.,Taylor, S.,Tomkinson, N.C.O.,Wall, I.,Watson, R.J.,Woolven, J.,Demont, E.H.
Optimization of a Series of 2,3-Dihydrobenzofurans as Highly Potent, Second Bromodomain (BD2)-Selective, Bromo and Extra-Terminal Domain (BET) Inhibitors.
J.Med.Chem., 64:10711-10741, 2021
Cited by
PubMed: 34260229
DOI: 10.1021/acs.jmedchem.1c00344
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.602 Å)
Structure validation

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