Design, Synthesis and Evaluation of a Series of 1,5-Diaryl-1,2,3-triazole-4-carbohydrazones as Inhibitors of the YAP-TAZ/TEAD Complex

被引:14
作者
Gibault, Floriane [1 ]
Sturbaut, Manon [1 ]
Coevoet, Mathilde [1 ]
Pugniere, Martine [5 ]
Burtscher, Ashley [2 ,3 ,4 ]
Allemand, Frederic [6 ]
Melnyk, Patricia [1 ]
Hong, Wanjin [7 ]
Rubin, Brian P. [2 ,3 ,4 ]
Pobbati, Ajaybabu V. [2 ,3 ,4 ]
Guichou, Jean-Francois [6 ]
Cotelle, Philippe [1 ,8 ]
Bailly, Fabrice [1 ]
机构
[1] Univ Lille, INSERM, UMR S 1172, Lille Neurosci & Cognit, F-59000 Lille, France
[2] Cleveland Clin, Lerner Res Inst, Robert J Tomsich Pathol & Lab Med Inst, Cleveland, OH 44195 USA
[3] Cleveland Clin, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
[4] Taussig Canc Ctr, Cleveland, OH 44195 USA
[5] Univ Montpellier, Inst Reg Canc Montpellier ICM, Inst Rech Cancerol Montpellier IRCM, 208 Rue Apothicaires, F-34298 Montpellier 5, France
[6] Univ Montpellier, CNRS, INSERM, UMR5048,U1054,Ctr Biol Struct, 29 Rue Navacelles, F-34090 Montpellier, France
[7] ASTAR, Inst Mol & Cell Biol, 61 Biopolis Dr, Singapore 138673, Singapore
[8] Ecole Cent Lille, F-59000 Lille, France
关键词
antitumor agents; Hippo pathway; protein-protein interaction; TEAD binding; YAP-TEAD inhibition; HIPPO SIGNALING PATHWAY; STRUCTURAL INSIGHTS; TEAD; YAP/TAZ;
D O I
10.1002/cmdc.202100153
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Starting from our previously reported hit, a series of 1,5-diaryl-1,2,3-triazole-4-carbohydrazones were synthesized and evaluated as inhibitors of the YAP/TAZ-TEAD complex. Their binding to hTEAD2 was confirmed by nanodifferential scanning fluorimetry, and some of the compounds were also found to moderately disrupt the YAP-TEAD interaction, as assessed by a fluorescence polarization assay. A TEAD luciferase gene reporter assay performed in HEK293T cells and RTqPCR measurements in MDA-MB231 cells showed that these compounds inhibit YAP/TAZ-TEAD activity to cells in the micromolar range. In spite of the cytotoxic effects displayed by some of the compounds of this series, they are still good starting points and can be suitably modified into an effective and viable YAP-TEAD disruptor in the future.
引用
收藏
页码:2823 / 2844
页数:22
相关论文
共 49 条
[1]   SYNTHESIS, CHARACTERIZATION, AND IN VITRO ANTIMICROBIAL EVALUATION OF HYDRAZONE AND BISHYDRAZONE DERIVATIVES OF ISATIN [J].
Adibi, Hadi ;
Khodaei, Mohammad Mehdi ;
Pakravan, Parvaneh ;
Abiri, Ramin .
PHARMACEUTICAL CHEMISTRY JOURNAL, 2010, 44 (04) :219-227
[2]   Titanium mediated olefination of aldehydes with α-haloacetates: an exceptionally stereoselective and general approach to (Z)-α-haloacrylatest [J].
Augustine, John Kallikat ;
Bombrun, Agnes ;
Venkatachaliah, Srinivasa ;
Jothi, Anandh .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2013, 11 (46) :8065-8072
[3]   The Hippo signaling pathway provides novel anti-cancer drug targets [J].
Bae, June Sung ;
Kim, Sun Mi ;
Lee, Ho .
ONCOTARGET, 2017, 8 (09) :16084-16098
[4]  
Barth M., 2017, patent, Patent No. 2017064277
[5]   Synthesis of new 1,2,3-triazolo[1,2-a]benzotriazoles or 2,3-benzo-1,3a,6,6a-tetraazapentalenes [J].
Biagi, G ;
Giorgi, I ;
Livi, O ;
Scartoni, V ;
Barili, PL .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1995, 32 (06) :1709-1714
[6]  
Buckman B. O., 2014, US Pat., Patent No. [2014/0200215, 20140200215]
[7]   Structural Insights into the Regulation of Hippo Signaling [J].
Cairns, Leah ;
Thao Tran ;
Kavran, Jennifer M. .
ACS CHEMICAL BIOLOGY, 2017, 12 (03) :601-610
[8]  
Chan P, 2016, NAT CHEM BIOL, V12, P282, DOI [10.1038/NCHEMBIO.2036, 10.1038/nchembio.2036]
[9]   Control of Proliferation and Cancer Growth by the Hippo Signaling Pathway [J].
Ehmer, Ursula ;
Sage, Julien .
MOLECULAR CANCER RESEARCH, 2016, 14 (02) :127-140
[10]   Repurposing of Drugs Targeting YAP-TEAD Functions [J].
Elisi, Gian Marco ;
Santucci, Matteo ;
D'Arca, Domenico ;
Lauriola, Angela ;
Marverti, Gaetano ;
Losi, Lorena ;
Scalvini, Laura ;
Bolognesi, Maria Laura ;
Mor, Marco ;
Costi, Maria Paola .
CANCERS, 2018, 10 (09)