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Development of small molecule inhibitors of natural killer group 2D receptor (NKG2D).

Authors :
Wang J
Nakafuku KM
Ziff J
Gelin CF
Gholami H
Thompson AA
Karpowich NK
Limon L
Coate HR
Damm-Ganamet KL
Shih AY
Grant JC
Côte M
Mak PA
Pascual HA
Rives ML
Edwards JP
Venable JD
Venkatesan H
Shi Z
Allen SJ
Sharma S
Kung PP
Shireman BT
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2023 Nov 15; Vol. 96, pp. 129492. Date of Electronic Publication: 2023 Sep 29.
Publication Year :
2023

Abstract

Natural killer group 2D (NKG2D) is a homodimeric activating immunoreceptor whose function is to detect and eliminate compromised cells upon binding to the NKG2D ligands (NKG2DL) major histocompatibility complex (MHC) molecules class I-related chain A (MICA) and B (MICB) and UL16 binding proteins (ULBP1-6). While typically present at low levels in healthy cells and tissue, NKG2DL expression can be induced by viral infection, cellular stress or transformation. Aberrant activity along the NKG2D/NKG2DL axis has been associated with autoimmune diseases due to the increased expression of NKG2D ligands in human disease tissue, making NKG2D inhibitors an attractive target for immunomodulation. Herein we describe the discovery and optimization of small molecule PPI (protein-protein interaction) inhibitors of NKG2D/NKG2DL. Rapid SAR was guided by structure-based drug design and accomplished by iterative singleton and parallel medicinal chemistry synthesis. These efforts resulted in the identification of several potent analogs (14, 21, 30, 45) with functional activity and improved LLE.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1464-3405
Volume :
96
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
37778428
Full Text :
https://doi.org/10.1016/j.bmcl.2023.129492