✦ LIBER ✦

Synthesis and Receptor Binding Studies of (±)l-Iodo-MK-801

✍ Scribed by David J. Yang; Brian J. Ciliax; Marcian E. Van Dort; David L. Gildersleeve; Jean-Luc Pirat; Anne B. Young; Donald M. Wieland

Book ID: 114421002
Publisher: Springer US
Year: 1989
Tongue: English
Weight: 502 KB
Volume: 06
Category: Article
ISSN: 0724-8741
DOI: 10.1023/a:1015912322247

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

(+)-3-[123I]Iodo-MK-801: Synthesis and c

(+)-3-[123I]Iodo-MK-801: Synthesis and characterization of binding to the N-methyl-D-aspartate receptor complex

✍ Richard W. Ransom; Wai-si Eng; H.Donald Burns; Raymond E. Gibson; Howard F. Solo 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 628 KB

P70 synthesis and binding affinities of

P70 synthesis and binding affinities of spacer-coupled (+)-MK-801 derivatives

✍ Dannhardt, G.; von Gruchalla, M. 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 147 KB

Regional potency differences of ifenprod

Regional potency differences of ifenprodil and other NMDA receptor antagonists in [3H]MK801 binding studies

✍ Klarica, M.; Carter, C. 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 153 KB

Rapid visualization of NMDA receptors in

Rapid visualization of NMDA receptors in the brain: characterization of (+)-3-[12I]-iodo-MK-801 binding to thin sections of rat brain

✍ William Jacobson; Georgia A. Cottrell 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 831 KB

Modulation of [3H]MK-801 binding to NMDA

Modulation of [3H]MK-801 binding to NMDA receptors in vivo and in vitro

✍ Fraser Murray; Jeffrey Kennedy; Peter H Hutson; Jason Elliot; Ian Huscroft; Kirs 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 165 KB

ChemInform Abstract: Aromatic Analogues

ChemInform Abstract: Aromatic Analogues of Arcaine Inhibit MK-801 Binding to the NMDA Receptor.

✍ Terre A. Sharma; Andrew J. Carr; Rebecca S. Davis; Ian J. Reynolds; Andrew D. Ha 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

Aromatic Analogues of Arcaine Inhibit MK-801 Binding to the NMDA Receptor. -A novel series of analogues such as (VII) and (IX) are synthesized. The most active compound is a derivative of (IX) without the methoxy substituent. The structure-activity relationships are discussed.