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7MCE

CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH 2-{(7P)-7-(1,4-dimethyl-1H-1,2,3-triazol-5-yl)-8-fluoro-5-[(S)-(oxan-4-yl)(phenyl)methyl]-5H-pyrido[3,2-b]indol-3-yl}propan-2-ol

Summary for 7MCE
Entry DOI10.2210/pdb7mce/pdb
DescriptorBromodomain-containing protein 4, 2-{(7P)-7-(1,4-dimethyl-1H-1,2,3-triazol-5-yl)-8-fluoro-5-[(S)-(oxan-4-yl)(phenyl)methyl]-5H-pyrido[3,2-b]indol-3-yl}propan-2-ol (3 entities in total)
Functional Keywordsbromodomain-containing protein 4 isoform long, brd4, bromodomain containing protein 4, cap, hunk1, mcap, mitotic chromosome associated protein sgc, cell cycle
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight15721.10
Authors
Sheriff, S. (deposition date: 2021-04-02, release date: 2021-09-29, Last modification date: 2023-10-18)
Primary citationHill, M.D.,Quesnelle, C.,Tokarski, J.,Fang, H.,Fanslau, C.,Haarhoff, Z.,Kramer, M.,Madari, S.,Wiebesiek, A.,Morrison, J.,Simmermacher-Mayer, J.,Sinz, M.,Westhouse, R.,Xie, C.,Zhao, J.,Huang, L.,Sheriff, S.,Yan, C.,Marsilio, F.,Everlof, G.,Zvyaga, T.,Lee, F.,Gavai, A.V.,Degnan, A.P.
Development of BET inhibitors as potential treatments for cancer: A new carboline chemotype.
Bioorg.Med.Chem.Lett., 51:128376-128376, 2021
Cited by
PubMed Abstract: We describe our efforts to introduce structural diversity to a previously described triazole-containing N1-carboline series of bromodomain and extra-terminal (BET) inhibitors. N9 carbolines were designed to retain favorable binding interactions that the N1-carbolines possess. A convergent synthetic route enabled modifications to reduce clearance, enhance physicochemical properties, and improve the overall in vitro profile. This work led to the identification of a potent BET inhibitor, (S)-2-{8-fluoro-5-[(3-fluoropyridin-2-yl)(oxan-4-yl)methyl]-7-[4-(H)methyl-1-methyl-1H-1,2,3-triazol-5-yl]-5H-pyrido[3,2-b]indol-3-yl}propan-2-ol (10), a compound with enhanced oral exposure in mice. Subsequent evaluation in a mouse triple-negative breast cancer tumor model revealed efficacy at 4 mg/kg of N9-carboline 10.
PubMed: 34560263
DOI: 10.1016/j.bmcl.2021.128376
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.76 Å)
Structure validation

238895

数据于2025-07-16公开中

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