ChemInform Abstract: Modifications of the 4,4′-Residues and SAR Studies of Biphalin, a Highly Potent Opioid Receptor Active Peptide.

ChemInform Abstract: Design and Synthesi

ChemInform Abstract: Design and Synthesis of a Novel Class of Highly Potent Selective and Orally Active Non-peptide Bradykinin B2 Receptor Antagonists

✍ Hiroshi Kayakiri; Yoshito Abe; Teruo Oku 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 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

ChemInform Abstract: Methylated Analogue

ChemInform Abstract: Methylated Analogues of Methyl (R)-4-(3,4-Dichlorophenylacetyl)-3- (pyrrolidin-1-ylmethyl)piperazine-1-carboxylate (GR-89,696) as Highly Potent ϰ-Receptor Agonists: Stereoselective Synthesis, Opioid-Receptor Affinity, Receptor Selectivity, and Functional Studies.

✍ Stella Soukara; Christoph A. Maier; Ursula Predoiu; Andreas Ehret; Rolf Jackisch 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 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

ChemInform Abstract: 2,2-Dicyanovinyl as

ChemInform Abstract: 2,2-Dicyanovinyl as a Nonaromatic Aryl Bioisostere: Synthesis, Binding Experiments, and SAR Studies of Highly Selective Dopamine D4 Receptor Ligands.

✍ Christian Haubmann; Harald Huebner; Peter Gmeiner 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

2,2-Dicyanovinyl as a Nonaromatic Aryl Bioisostere: Synthesis, Binding Experiments, and SAR Studies of Highly Selective Dopamine D4 Receptor Ligands. -Title compounds of type (I) are tested for their dopamine receptor binding activity. Both types of 4-or 5-substituted compounds show selective dopami

ChemInform Abstract: Studies on the Synt

ChemInform Abstract: Studies on the Synthesis of Cholecystokinin A Receptor Antagonists. Part 4. Synthesis and Cholecystokinin A Receptor Inhibitory Activities of Benzimidazole Derivatives

✍ Y. AJISAWA; K. AKAHANE; M. AKAHANE; K. SATO; T. TAMAI; M. SAITO; N. TANAKA; K. K 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

ChemInform Abstract: Design, Synthesis,

ChemInform Abstract: Design, Synthesis, and Antitumor Activity of 4′-Thionucleosides as Potent and Selective Agonists at the Human A3 Adenosine Receptor

✍ Lak Shin Jeong; et al. et al. 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 15 KB 👁 2 views

ChemInform Abstract: 1-(2-Nitrophenyl)th

ChemInform Abstract: 1-(2-Nitrophenyl)thiosemicarbazides: A Novel Class of Potent, Orally Active Non-Peptide Antagonists for the Bradykinin B2 Receptor.

✍ Edward K. Dziadulewicz; et al. et al. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views