| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1369635 | Bioorganic & Medicinal Chemistry Letters | 2012 | 6 Pages |
Abstract
A series of 5-alkylaminolquinolines was designed and synthesized as potential novel CRF1 receptor antagonists. The structure–activity relationships (SARs) of the substituents on each position (R2, R3, R5 and R5′) were investigated.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kunitoshi Takeda, Taro Terauchi, Kogyoku Shin, Mitsuhiro Ino, Hisashi Shibata, Masahiro Yonaga,