Design and synthesis of tri-substituted pyrimidine derivatives as bifunctional tumor immunotherapeutic agents targeting both A2A adenosine receptors and histone deacetylases-Reference-Cited by-同舟云学术

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Design and synthesis of tri-substituted pyrimidine derivatives as bifunctional tumor immunotherapeutic agents targeting both A2A adenosine receptors and histone deacetylases

Published:2024-01 Issue:1 Volume:35 Page:108136
ISSN:1001-8417
Container-title:Chinese Chemical Letters
language:en
Short-container-title:Chinese Chemical Letters

Author:

Liu Ruiquan,Duan Wenwen,Yan Wenzhong,Zhang Jinfeng,Cheng Jianjun^ORCID

Publisher

Elsevier BV

Subject

General Chemistry

Reference30 articles.

1. Targeting immunosuppressive adenosine in cancer

2. International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and Classification of Adenosine Receptors—An Update

3. Role of G-protein-coupled adenosine receptors in downregulation of inflammation and protection from tissue damage

4. A2A adenosine receptor protects tumors from antitumor T cells

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1. Interaction of Purine and its Derivatives with A1, A2-Adenosine Receptors and Vascular Endothelial Growth Factor Receptor-1 (Vegf-R1) as a Therapeutic Alternative to Treat Cancer;Drug Research;2024-08-22

2. A highly sensitive ratiometric fluorescence immunoassay based on bioorthogonal nanozymes;Chemical Communications;2024

3. Discovery of the ((diaryl)methyl)phosphonic acid derivatives as novel CD73 inhibitors;Journal of Heterocyclic Chemistry;2023-08-28

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