✦ LIBER ✦

ChemInform Abstract: Synthesis and Structure-Activity Relationships of 1,2,3,4- Tetrahydroquinoline-2,3,4-trione 3-Oximes: Novel and Highly Potent Antagonists for NMDA Receptor Glycine Site.

✍ Scribed by S. X. CAI; Z.-L. ZHOU; J.-C. HUANG; E. R. WHITTEMORE; Z. O. EGBUWOKU; Y. LUE; J. E. HAWKINSON; R. M. WOODWARD; E. WEBER; J. F. W. KEANA

Book ID: 112041062
Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199649166

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Structure−Activity Relatio

Synthesis and Structure−Activity Relationships of 1,2,3,4-Tetrahydroquinoline-2,3,4-trione 3-Oximes: Novel and Highly Potent Antagonists for NMDA Receptor Glycine Site

✍ Cai, Sui Xiong; Zhou, Zhang-Lin; Huang, Jin-Cheng; Whittemore, Edward R.; Egbuwo 📂 Article 📅 1996 🏛 American Chemical Society 🌐 English ⚖ 267 KB

ChemInform Abstract: Synthesis and Struc

ChemInform Abstract: Synthesis and Structure-Activity Relationships of Substituted 1,4- Dihydroquinoxaline-2,3-diones: Antagonists of N-Methyl-D-aspartate ( NMDA) Receptor Glycine Sites and Non-NMDA Glutamate Receptors.

✍ J. F. W. KEANA; S. M. KHER; S. X. CAI; C. M. DINSMORE; A. G. GLENN; J. GUASTELLA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: Novel 5-Hydroxytryp

ChemInform Abstract: Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. Synthesis and Structure-Activity Relationships of 9-Methyl-2,3,4,9- tetrahydrothiopyrano(2,3-b)indol-4-one Derivatives.

✍ T. SUZUKI; A. MATSUHISA; K. MIYATA; I. YANAGISAWA; M. OHTA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

ChemInform Abstract: Synthesis of 8-Chlo

ChemInform Abstract: Synthesis of 8-Chloro-4,5-dihydro-1H-benzo[e][1,4]-diazepine-2,3-diones as Potential NMDA Receptor Glycine Site Antagonists.

✍ Ki-Jun Hwang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Synthesis and structure–Activity relatio

Synthesis and structure–Activity relationships of thieno[2,3-d]pyrimidine-2,4-dione derivatives as potent GnRH receptor antagonists

✍ Zhiqiang Guo; Yongsheng Chen; Dongpei Wu; Yun-Fei Zhu; R.Scott Struthers; John S 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 221 KB

The synthesis and SAR studies of thieno [2,3-d]pyrimidine-2,4-diones as human GnRH receptor antagonists to treat reproductive diseases are discussed. It was found that the 2-(2-pyridyl)ethyl group on the 5-aminomethyl functionality of the core structure was a key feature for good receptor binding ac

Synthesis and Structure—Activity Relatio

Synthesis and Structure—Activity Relationships of Thieno[2,3-d]pyrimidine-2,4-dione Derivatives as Potent GnRH Receptor Antagonists.

✍ Zhiqiang Guo; Yongsheng Chen; Dongpei Wu; Yun-Fei Zhu; R. Scott Struthers; John 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 92 KB 👁 2 views