Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives-Reference-Cited by-同舟云学术

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Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives

Published:2015-08 Issue:16 Volume:25 Page:3368-3372
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Suzuki Shinya,Okano Tsubasa,Horiuchi Rie,Hareyama Nana,Amikura Kazutoshi,Yamamoto Naoyoshi,Yoshizawa Yoshitaka,Yagi Mai,Serizawa Kanako,Hayashi Ryoji

Publisher

Elsevier BV

Subject

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

Reference12 articles.

1. Ligand design for α 1 adrenoceptor subtype selective antagonists

2. The α1L -adrenoceptor is an alternative phenotype of the α1A -adrenoceptor

3. Identification of Cysteine-Rich Epidermal Growth Factor–Like Domain 1α (CRELD1α) as a Novel α1A-Adrenoceptor–Down-Regulating Protein and Establishment of an α1L-Adrenoceptor–Expressing Cell Line

4. Native profiles of α1A -adrenoceptor phenotypes in rabbit prostate

5. α1L-Adrenoceptors mediate contractions of the isolated mouse prostate

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. What makes the α 1A ‐adrenoceptor gene product assume an α 1L ‐adrenoceptor phenotype?;British Journal of Pharmacology;2019-03-27

2. Ene reactions of 2-borylated α-methylstyrenes: a practical route to 4-methylenechromanes and derivatives;Organic & Biomolecular Chemistry;2019

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