Advances in the discovery of activin receptor-like kinase 5 (ALK5) inhibitors

被引:3
作者
Mansour, Mai A. [1 ]
Hassan, Ghaneya S. [1 ,2 ]
Serya, Rabah A. T. [3 ]
Jaballah, Maiy Y. [3 ]
Abouzid, Khaled A. M. [3 ]
机构
[1] Badr Univ Cairo, Sch Pharm, Pharmaceut Chem Dept, Cairo, Egypt
[2] Cairo Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo, Egypt
[3] Ain Shams Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo, Egypt
关键词
TGF-beta; ALK5; inhibitors; Binding interactions; Structure-activity relationship; TGF-BETA RECEPTOR; TO-MESENCHYMAL TRANSITION; SMALL-MOLECULE INHIBITOR; I RECEPTOR; BIOLOGICAL EVALUATION; DOMAIN INHIBITORS; POTENT; DESIGN; FIBROSIS; DERIVATIVES;
D O I
10.1016/j.bioorg.2024.107332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activin receptor-like kinase-5 (ALK5) is an outstanding member of the transforming growth factor-beta (TGF-beta) family. (TGF-beta) signaling pathway integrates pleiotropic proteins that regulate various cellular processes such as growth, proliferation, and differentiation. Dysregulation within the signaling pathway can cause variety of diseases, such as fibrosis, cardiovascular disease, and especially cancer, rendering ALK5 a potential drug target. Hence, various small molecules have been designed and synthesized as potent ALK5 inhibitors. In this review, we shed light on the current ATP-competitive inhibitors of ALK5 through diverse heterocyclic based scaffolds that are in clinical or pre-clinical phases of development. Moreover, we focused on the binding interactions of the compounds to the ATP binding site and the structure-activity relationship (SAR) of each scaffold, revealing new scopes for designing novel candidates with enhanced selectivity and metabolic profiles.
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页数:16
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共 108 条
  • [81] LY3200882, a novel, highly selective TGFβRI small molecule inhibitor
    Pei, Huaxing
    Parthasarathy, Saravanan
    Joseph, Sajan
    McMillen, William
    Xu, Xiaohong
    Castaneda, Stephen
    Inigo, Ivan
    Britt, Karen
    Anderson, Bryan
    Zhao, Gaiying
    Sawyer, Scott
    Beight, Douglas
    Kaoudi, Talbi
    Iyer, Chandrasekar
    Bian, Huimin
    Pappas, Amy
    Surguladze, David
    Schaer, David
    Benhadji, Karim
    Kalos, Michael
    Driscoll, Kyla
    [J]. CANCER RESEARCH, 2017, 77
  • [82] IMMUNOHISTOCHEMICAL LOCALIZATION OF TGF-BETA-1, TGF-BETA-2, AND TGF-BETA-3 IN THE MOUSE EMBRYO - EXPRESSION PATTERNS SUGGEST MULTIPLE ROLES DURING EMBRYONIC-DEVELOPMENT
    PELTON, RW
    SAXENA, B
    JONES, M
    MOSES, HL
    GOLD, LI
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 115 (04) : 1091 - 1105
  • [83] Local Release of TGF-ß Inhibitor Modulates Tumor-Associated Neutrophils and Enhances Pancreatic Cancer Response to Combined Irreversible Electroporation and Immunotherapy
    Peng, Huiming
    Shen, Jian
    Long, Xin
    Zhou, Xiaoqi
    Zhang, Jiaqi
    Xu, Xina
    Huang, Teng
    Xu, Hui
    Sun, Shuguo
    Li, Chun
    Lei, Ping
    Wu, Heshui
    Zhao, Jun
    [J]. ADVANCED SCIENCE, 2022, 9 (10)
  • [84] ALK5 kinase inhibitory activity and synthesis of 2,3,4-substituted 5,5-dimethyl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazoles
    Reznickova, Eva
    Tenora, Lukas
    Pospisilova, Pavlina
    Galeta, Juraj
    Jorda, Radek
    Berka, Karel
    Majer, Pavel
    Potacek, Milan
    Krystof, Vladimir
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 127 : 632 - 642
  • [85] Design, Synthesis, and Evaluation of Indolinones as Inhibitors of the Transforming Growth Factor β Receptor I (TGFβRI)
    Roth, Gerald J.
    Heckel, Armin
    Brandl, Trixi
    Grauert, Matthias
    Hoerer, Stefan
    Kley, Joerg T.
    Schnapp, Gisela
    Baum, Patrick
    Mennerich, Detlev
    Schnapp, Andreas
    Park, John E.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (20) : 7287 - 7295
  • [86] Design, synthesis and optimization of 7-substituted-pyrazolo[4,3-b] pyridine ALK5 (activin receptor-like kinase 5) inhibitors
    Sabat, Mark
    Wang, Haixia
    Scorah, Nick
    Lawson, J. David
    Atienza, Joy
    Kamran, Ruhi
    Hixon, Mark S.
    Dougan, Douglas R.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 27 (09) : 1955 - 1961
  • [87] ALK5 promotes tumor angiogenesis by upregulating matrix metalloproteinase-9 in tumor cells
    Safina, A.
    Vandette, E.
    Bakin, A. V.
    [J]. ONCOGENE, 2007, 26 (17) : 2407 - 2422
  • [88] Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain
    Sawyer, JS
    Beight, DW
    Britt, KS
    Anderson, BD
    Campbell, RM
    Goodson, T
    Herron, DK
    Li, HY
    McMillen, WT
    Mort, N
    Parsons, S
    Smith, ECR
    Wagner, JR
    Yan, L
    Zhang, FM
    Yingling, JM
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (13) : 3581 - 3584
  • [89] Synthesis and activity of new aryl- and heteroaryl- substituted pyrazole inhibitors of the transforming growth factor-b type I receptor kinase domain
    Sawyer, JS
    Anderson, BD
    Beight, DW
    Campbell, RM
    Jones, ML
    Herron, DK
    Lampe, JW
    McCowan, JR
    McMillen, WT
    Mort, N
    Parsons, S
    Smith, ECR
    Vieth, M
    Wier, LC
    Yan, L
    Zhang, FM
    Yingling, JM
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (19) : 3953 - 3956
  • [90] TGF-β1 induces erlotinib resistance in non-small cell lung cancer by down-regulating PTEN
    Shen, Hua
    Guan, Dan
    Shen, Jianxin
    Wang, Min
    Chen, Xiaofeng
    Xu, Tongpeng
    Liu, Lianke
    Shu, Yongqian
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2016, 77 : 1 - 6