Synthesis and Biological Activity of Various Derivatives of a Novel Class of Potent, Selective, and Orally Active Prostaglandin D2 Receptor Antagonists. 1. Bicyclo[2.2.1]heptane Derivatives-Reference-Cited by-同舟云学术

Synthesis and Biological Activity of Various Derivatives of a Novel Class of Potent, Selective, and Orally Active Prostaglandin D2 Receptor Antagonists. 1. Bicyclo[2.2.1]heptane Derivatives

Published:2003-05-10 Issue:12 Volume:46 Page:2436-2445
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mitsumori Susumu¹,Tsuri Tatsuo¹,Honma Tsunetoshi¹,Hiramatsu Yoshiharu¹,Okada Toshihiko¹,Hashizume Hiroshi¹,Inagaki Masanao¹,Arimura Akinori¹,Yasui Kiyoshi¹,Asanuma Fujio¹,Kishino Junji¹,Ohtani Mitsuaki¹

Affiliation:

1. Shionogi Research Laboratories, Shionogi & Co., Ltd., 12-4, Sagisu 5-chome, Fukushima-ku, Osaka 553-0002, Japan

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm020517g

Reference57 articles.

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3. Prostacyclin-analogs

4. Prostaglandins and congeners. 7. Synthesis of simplified prostaglandins. Inhibition of gastric acid secretion by 2-(.omega.-carboxyalkyl)-3-alkylcycloalkanones

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