8OU4

Cereblon isoform 4 in complex with novel Benzamide-Type Cereblon Binder 11a

8OU4 の概要

• エントリーDOI: 10.2210/pdb8ou4/pdb
• 分子名称: Cereblon isoform 4, ZINC ION, 4-azanyl-~{N}-[(3~{S})-2,6-bis(oxidanylidene)piperidin-3-yl]-2-chloranyl-benzamide, ... (4 entities in total)
• 機能のキーワード: cereblon, protac, e3, molecular glue, signaling protein
• 由来する生物種: Magnetospirillum gryphiswaldense
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 41870.35

構造登録者

Heim, C.,Bischof, L.,Hartmann, M.D. (登録日: 2023-04-21, 公開日: 2023-11-15, 最終更新日: 2023-11-22)

主引用文献

Steinebach, C.,Bricelj, A.,Murgai, A.,Sosic, I.,Bischof, L.,Ng, Y.L.D.,Heim, C.,Maiwald, S.,Proj, M.,Voget, R.,Feller, F.,Kosmrlj, J.,Sapozhnikova, V.,Schmidt, A.,Zuleeg, M.R.,Lemnitzer, P.,Mertins, P.,Hansen, F.K.,Gutschow, M.,Kronke, J.,Hartmann, M.D.
Leveraging Ligand Affinity and Properties: Discovery of Novel Benzamide-Type Cereblon Binders for the Design of PROTACs.
J.Med.Chem., 66:14513-14543, 2023

PubMed Abstract: Immunomodulatory imide drugs (IMiDs) such as thalidomide, pomalidomide, and lenalidomide are the most common cereblon (CRBN) recruiters in proteolysis-targeting chimera (PROTAC) design. However, these CRBN ligands induce the degradation of IMiD neosubstrates and are inherently unstable, degrading hydrolytically under moderate conditions. In this work, we simultaneously optimized physiochemical properties, stability, on-target affinity, and off-target neosubstrate modulation features to develop novel nonphthalimide CRBN binders. These efforts led to the discovery of conformationally locked benzamide-type derivatives that replicate the interactions of the natural CRBN degron, exhibit enhanced chemical stability, and display a favorable selectivity profile in terms of neosubstrate recruitment. The utility of the most potent ligands was demonstrated by their transformation into potent degraders of BRD4 and HDAC6 that outperform previously described reference PROTACs. Together with their significantly decreased neomorphic ligase activity on IKZF1/3 and SALL4, these ligands provide opportunities for the design of highly selective and potent chemically inert proximity-inducing compounds.

PubMed: 37902300
DOI: 10.1021/acs.jmedchem.3c00851

実験手法

X-RAY DIFFRACTION (2.25 Å)