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Guanidine-acylguanidine bioisosteric approach to address peptidergic receptors: pharmacological and diagnostic tools for the NPY Y1 receptor and versatile building blocks based on arginine substitutes

机译：胍基-酰基胍生物立体异构方法解决肽能受体：NPY Y1受体的药理学和诊断工具以及基于精氨酸替代物的通用构建基块

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Keller Max;
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年度 2009
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正文语种 {"code":"de","name":"German","id":7}
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1. Application of the Guanidine-Acylguanidine Bioisosteric Approach to Argininamide-Type NPY Y2 Receptor Antagonists [J] . Nikola Pluym, Albert Brennauer, Max Keller ChemMedChem . 2011,第9期

机译：胍基-酰基胍生物立体异构方法在精氨酸酰胺型NPY Y2受体拮抗剂中的应用
2. Red-fluorescent argininamide-type NPY Y1 receptor antagonists as pharmacological tools. [J] . Keller M, Erdmann D, Pop N, Bioorganic and medicinal chemistry . 2011,第9期

机译：红色荧光精氨酸酰胺型NPY Y1受体拮抗剂作为药理学工具。
3. Guanidine-Acylguanidine Bioisosteric Approach in the Design of Radioligands: Synthesis of a Tritium-Labeled N-G-Propionylargininamide ([H-3]-UR-MK114) as a Highly Potent and Selective Neuropeptide Y Y-1 Receptor Antagonist [J] . Keller M, Pop N, Hutzler C, Journal of Medicinal Chemistry . 2008,第24期

机译：放射性配体设计中的胍基-酰基胍基生物立体方法：Tri标记的N-G-丙二酰精氨酰胺（[H-3] -UR-MK114）的合成作为高强度和选择性神经肽Y Y-1受体拮抗剂。
4. Cellular and pharmacological characterization of NPY Y1 receptor expression in cultured rat hippocampal neurons and astrocytes. [D] . St. Pierre, Jacques-Andre. 2000

机译：培养的大鼠海马神经元和星形胶质细胞中NPY Y1受体表达的细胞和药理学表征。
5. Small-Molecule Lysophosphatidic Acid Receptor 5 (LPAR5) Antagonists: Versatile Pharmacological Tools to Regulate Inflammatory Signaling in BV-2 Microglia Cells [O] . Ioanna Plastira, Lisha Joshi, Eva Bernhart, 2019

机译：小分子溶血磷脂酸受体5（LPAR5）拮抗剂：通用药理学工具用于调节BV-2微胶质细胞中的炎症信号
6. Synthesis and characterization of subtype-selective estrogen receptor ligands and their application as pharmacological tools - Cross-talk between estrogen and NPY Y1 receptors in human breast cancer cells [O] . Memminger Martin 2009

机译：亚型选择性雌激素受体配体的合成，表征及其作为药理学工具的应用-人类乳腺癌细胞中雌激素和NPY Y1受体之间的串扰

Guanidine-acylguanidine bioisosteric approach to address peptidergic receptors: pharmacological and diagnostic tools for the NPY Y1 receptor and versatile building blocks based on arginine substitutes

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