✦ LIBER ✦

New piperidinyl- and 1,2,3,6-tetrahydropyridinyl-pyrimidine derivatives as selective 5-HT1A receptor agonists with highly potent anti-ischemic effects

✍ Scribed by Katsuhide Kamei; Noriko Maeda; Ryoko Katsuragi-Ogino; Makoto Koyama; Mika Nakajima; Toshio Tatsuoka; Tomochika Ohno; Teruyoshi Inoue

Book ID: 108073660
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 226 KB
Volume: 15
Category: Article
ISSN: 0960-894X
DOI: 10.1016/j.bmcl.2005.04.059

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

New Piperidinyl- and 1,2,3,6-Tetrahydrop

New Piperidinyl- and 1,2,3,6-Tetrahydropyridinyl-pyrimidine Derivatives as Selective 5-HT1A Receptor Agonists with Highly Potent anti-Ischemic Effects.

✍ Katsuhide Kamei; Noriko Maeda; Ryoko Katsuragi-Ogino; Makoto Koyama; Mika Nakaji 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

ChemInform Abstract: New 5-HT1A Receptor

ChemInform Abstract: New 5-HT1A Receptor Agonists Possessing 1,4-Benzoxazepine Scaffold Exhibit Highly Potent Anti-Ischemic Effects.

✍ Katsuhide Kamei; Noriko Maeda; Ryoko Ogino; Makoto Koyama; Mika Nakajima; Toshio 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Discovery of N1-(6-Chloroimidazo[2,1-b][

Discovery of N1-(6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonyl)tryptamine as a Potent, Selective, and Orally Active 5-HT6 Receptor Agonist

✍ Stock, Joseph R.; Lennox, William J.; Bernotas, Ronald C.; Ellingboe, John W.; B 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 168 KB

ChemInform Abstract: 2-Substituted 5,6-D

ChemInform Abstract: 2-Substituted 5,6-Dimethyl-3-phenylsulfonyl-pyrazolo[1,5-a]pyrimidines: New Series of Highly Potent and Specific Serotonin 5-HT6 Receptor Antagonists.

✍ Alexandre V. Ivachtchenko; Elena S. Golovina; Madina G. Kadieva; Angela G. Korya 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 22 KB 👁 1 views

## Abstract Synthesis, biological evaluation, and SAR for novel title compounds (I) are disclosed.

Synthesis of (1S,3aS)-8-(2,3,3a,4,5,6-he

Synthesis of (1S,3aS)-8-(2,3,3a,4,5,6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like properties

✍ Jürgen Wichmann; Geo Adam; Stephan Röver; Michael Hennig; Michelangelo Scalone; 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 363 KB

Structure–Activity Relationship Study of

Structure–Activity Relationship Study of N 6 -(2-(4-(1 H -Indol-5-yl)piperazin-1-yl)ethyl)- N 6 -propyl-4,5,6,7-tetrahydrobenzo[ d ]thiazole-2,6-diamine Analogues: Development of Highly Selective D3 Dopamine Receptor Agonists along with a Highly Potent D2/D3 Agonist and Their Pharmacological Characterization

✍ Johnson, Mark; Antonio, Tamara; Reith, Maarten E. A.; Dutta, Aloke K. 📂 Article 📅 2012 🏛 American Chemical Society 🌐 English ⚖ 918 KB