Tetrahydroquinoline and tetrahydroisoquinoline derivatives as potential selective PDE4B inhibitors-Reference-Cited by-同舟云学术

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Tetrahydroquinoline and tetrahydroisoquinoline derivatives as potential selective PDE4B inhibitors

Published:2018-10 Issue:19 Volume:28 Page:3271-3275
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Li Ya-Sheng,Liu Xing-Yu,Zhao Dong-Sheng,Liao Yi-Xian,Zhang Lian-Hui,Zhang Feng-Zhi,Song Gao-Peng,Cui Zi-Ning

Funder

National Key Research and Development Program of China

National Key Project for Basic Research

Special Fund for the Research and Construction of Public Service Ability

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. O’ Donnell;Raghavan;Curr Opin Pharmacol,2011

2. Phosphodiesterase: overview of protein structures, potential therapeutic applications and recent progress in drug development

3. The Next Generation of Phosphodiesterase Inhibitors: Structural Clues to Ligand and Substrate Selectivity of Phosphodiesterases

4. Primary sequence of cyclic nucleotide phosphodiesterase isozymes and the design of selective inhibitors

5. Localized Effects of cAMP Mediated by Distinct Routes of Protein Kinase A

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1. Targeting next-generation PDE4 inhibitors in search of potential management of rheumatoid arthritis and psoriasis;Bioorganic Chemistry;2024-10

2. Design, synthesis, and in vitro biological evaluation of novel HDAC inhibitors bearing C-1 phenyl substituted tetrahydroisoquinoline Cap moiety as anti-tumor therapeutic agents;Medicinal Chemistry Research;2024-03-27

3. Synthesis, In Silico, and In Vitro Biological Evaluation of New Furan Hybrid Molecules;Processes;2022-10-02

4. Influence of heat processing on the anti-inflammatory activity of fresh Smilax glabra based on PDE4 inhibition;Food Chemistry: X;2022-10

5. Convenient synthesis of 8‐aryl‐6‐aryl‐1,2,3,4‐tetrahydroisoquinoline‐5,7‐dicarbonitriles via a cascade Michael/cyclization reaction;Journal of the Chinese Chemical Society;2022-03-30

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