Rational Design, Synthesis, Biological Evaluation, Homology and Docking Studies of Coumarin Derivatives as α1-Adrenoceptor Antagonists-Reference-Cited by-同舟云学术

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Rational Design, Synthesis, Biological Evaluation, Homology and Docking Studies of Coumarin Derivatives as α1-Adrenoceptor Antagonists

Published:2011-06 Issue:6 Volume:8 Page:1052-1064
ISSN:1612-1872
Container-title:Chemistry & Biodiversity
language:en
Short-container-title:Chemistry & Biodiversity

Author:

Zhou Xiang,Chen Ya-Dong,Wang Tao,Wang Xiao-Bing,Kong Ling-Yi

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

Reference23 articles.

1. ?1 Adrenoceptor subtypes: A synopsis of their pharmacology and molecular biology

2. Pharmacological Options in the Treatment of Benign Prostatic Hyperplasia

3. Identification of alpha1A-adrenoceptor selective antagonists for the treatment of benign prostatic hyperplasia

4. .alpha.- and .beta.-Adrenoceptors: From the Gene to the Clinic. 2. Structure-Activity Relationships and Therapeutic Applications

5. .alpha.- and .beta.-Adrenoceptors: From the Gene to the Clinic. Part 1. Molecular Biology and Adrenoceptor Subclassification

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1. Identification of a Novel Subtype-Selective α_1B-Adrenoceptor Antagonist;ACS Chemical Neuroscience;2024-01-18

2. The one-pot synthesis of butyl-1H-indol-3-alkylcarboxylic acid derivatives in ionic liquid as potent dual-acting agent for management of BPH;European Journal of Medicinal Chemistry;2020-11

3. Synthesis, structure elucidation, DNA-PK, PI3K, anti-platelet and anti-bacteria activity of linear 5, 6, and 10-substituted-2-morpholino-chromen-oxazine-dione and angular 3, 4, 6-substituted-8-morpholino-chromen-oxazine-2,10-dione;Journal of Enzyme Inhibition and Medicinal Chemistry;2016-06-02

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