Lead Development of SL-3111 ; Exploration of A Second Generation of Non-peptide Peptide Mimetics for Potent and Selective δ-Opioid Receptor Agonists
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概要
- 論文の詳細を見る
- 2001-03-01
著者
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HRUBY Victor
Department of Chemistry, University of Arizona
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Hruby Victor
Dept. Of Chemistry Univ. Of Arizona
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Hruby Victor
Department Of Chemistry University Of Arizona
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Okayama Toru
Department Of Chemistry University Of Arizona
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DAVIS Peg
Pharmacology, Univ. of Arizona
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YAMAMURA Henry
Pharmacology, Univ. of Arizona
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PORRECA Frank
Pharmacology, Univ. of Arizona
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Davis Peg
Pharmacology Univ. Of Arizona
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WEI Hongbing
Pharmacology, University of Arizona
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Wei Hongbing
Pharmacology University Of Arizona
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Porreca Frank
Pharmacology Univ. Of Arizona
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Yamamura Henry
Pharmacology Univ. Of Arizona
関連論文
- Small and Local Structural Modifications Induced Large Change in Bioactivity and Membrane-bound Conformation of Dual Acting Opioid Agonist/NK1 antagonist
- γ-Functional Prolines Based on Naturally Occurring Hydroxyproline. II
- Biological Evaluations of Cyclic Bifunctional Peptide Derivatives Possessing Opioid Agonist and NK1 Antagonist Activities
- Lead Development of SL-3111 ; Exploration of A Second Generation of Non-peptide Peptide Mimetics for Potent and Selective δ-Opioid Receptor Agonists
- γ-Functional Prolines Based on Naturally Occurring Hydroxyproline.
- APPLICATION OF 4-ALKOXY-2- HYDROXYBENZALDEHYDE (AHB) LINKER TO SOLID PHASE SYNTHESIS OF BIPHALIN ; DIMERIC PEPTIDE CONNECTED AT C-TERMINI THROUGH HYDRAZINE
- Search for Naturally Occurring Substances for Prevention against the Complications of Diabetes : Inhibitory Effect on Aldose Reductase and Platelet Aggregation