Synthesis, Screening, and Molecular Modeling of New Potent and Selective Antagonists at the α1d Adrenergic Receptor-Reference-Cited by-同舟云学术

Synthesis, Screening, and Molecular Modeling of New Potent and Selective Antagonists at the α1d Adrenergic Receptor

Published:2004-03-12 Issue:8 Volume:47 Page:1900-1918
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Leonardi Amedeo¹,Barlocco Daniela¹,Montesano Federica¹,Cignarella Giorgio¹,Motta Gianni¹,Testa Rodolfo¹,Poggesi Elena¹,Seeber Michele¹,De Benedetti Pier G.¹,Fanelli Francesca¹

Affiliation:

1. Pharmaceutical R & D Division, Recordati s.p.a., Via Civitali 1, 20148 Milano, Italy, Pharmaco-Chemistry and Toxicology Institute, University of Milano, V.le Abruzzi 42, 20131 Milano, Italy, Department of Chemistry, University of Modena and Reggio Emilia, Via Campi 183, 41100 Modena, Italy, and Dulbecco Telethon Institute (DTI) and Department of Chemistry, University of Modena and Reggio Emilia, Via Campi 183, 41100 Modena, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm030944%2B

Reference43 articles.

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

2. Vasodilatation elicited by 5-HT1A receptor agonists in constant-pressore-perfused rat kidney is mediated by blockade of α1A-adrenoceptors

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