Design and synthesis of novel 3-substituted-indole derivatives as selective H3 receptor antagonists and potent free radical scavengers-Reference-Cited by-同舟云学术

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Design and synthesis of novel 3-substituted-indole derivatives as selective H3 receptor antagonists and potent free radical scavengers

Published:2013-10 Issue:19 Volume:21 Page:5936-5944
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Tang Li,Zhao Liying,Hong Lingjuan,Yang Fenyan,Sheng Rong,Chen Jianzhong,Shi Ying,Zhou Naimin,Hu Yongzhou

Funder

National Natural Science Foundation of China

Ministry of Science and Technology

Zhejiang Provincial Natural Foundation of China

Pharmaceutical Informatics Institute, Zhejiang University

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor

2. Cloning and Functional Expression of the Human Histamine H3Receptor

3. Increase of acetylcholine release from cortex of freely moving rats by administration of histamine into the nucleus basalis magnocellularis

4. Histamine inhibits dopamine release in the mouse striatum via presynaptic H3 receptors

5. The histamine H3 receptor as a therapeutic drug target for CNS disorders

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1. -Proline catalyzed synthesis of biologically promising heterocycles under sustainable conditions;Tetrahedron Chem;2024-08

2. Synthesis and structure-activity optimization of hydroxypyridinones against rhabdomyolysis-induced acute kidney injury;European Journal of Medicinal Chemistry;2024-01

3. Benzimidazole-derived Compounds Designed for Different Targets of Alzheimer’s Disease;Current Medicinal Chemistry;2019-09-02

4. Histamine H 3 receptor ligands by hybrid virtual screening, docking, molecular dynamics simulations, and investigation of their biological effects;Chemical Biology & Drug Design;2019-01-24

5. Application and comparison of the catalytic activity of Fe3O4 MNPs, Kaolin and Montmorillonite K10 for the synthesis of indole derivatives;EURASIAN CHEM COMMUN;2019

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