Three Candesartan Salts with Enhanced Oral Bioavailability-Reference-Cited by-同舟云学术

Three Candesartan Salts with Enhanced Oral Bioavailability

Published:2015-07-10 Issue:8 Volume:15 Page:3707-3714
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Chi Yingnan¹,Xu Wenting¹,Yang Yan²,Yang Zhichao²,Lv Hongjin³,Yang Song¹,Lin Zhengguo¹,Li Jikun¹,Gu Jingkai²,Hill Craig L.³,Hu Changwen¹

Affiliation:

1. Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic, School of Chemistry, Beijing Institute of Technology, Beijing 100081, P. R. China

2. Research Center for Drug Metabolism, Jilin University, Changchun 130012, P. R. China

3. Department of Chemistry, Emory University, 1515 Dickey Drive, Atlanta, Georgia 30322, United States

Funder

National Natural Science Foundation of China

Ministry of Education of the People's Republic of China

Ministry of Science and Technology of the People's Republic of China

State Administration of Foreign Experts Affairs

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.cgd.5b00297

Reference48 articles.

1. Candesartan

2. Clinical Pharmacokinetics of Candesartan

3. Nonpeptide angiotensin II receptor antagonists. Synthesis and biological activity of benzimidazolecarboxylic acids

4. Inhibition of rabbit aortic angiotensin II (AII) receptor by CV-11974, a new nonpeptide AII antagonist

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