Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors-Reference-Cited by-同舟云学术

Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors

Published:2019-08 Issue:16 Volume:27 Page:3692-3706
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Chino Ayaka,Honda Shugo,Morita Masataka,Yonezawa Koichi,Hamaguchi Wataru,Amano Yasushi,Moriguchi Hiroyuki,Yamazaki Mayako,Aota Masaki,Tomishima Masaki,Masuda Naoyuki

Publisher

Elsevier BV

Subject

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

Reference40 articles.

1. A Systematic Review of the Prevalence of Schizophrenia

2. Schizophrenia, “just the facts” 4. Clinical features and conceptualization

3. Isolation and characterization of a dual-substrate phosphodiesterase gene family: PDE10A

4. Isolation and characterization of PDE10A, a novel human 3′, 5′-cyclic nucleotide phosphodiesterase

5. Cloning and Characterization of a Novel Human Phosphodiesterase That Hydrolyzes Both cAMP and cGMP (PDE10A)

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