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6β-N-Heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists

机译：6β-N-杂环取代的纳丙胺衍生物午间作为潜在的导致外周Mu阿片受体选择性拮抗剂

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Yunyun Yuan; David L. Stevens; Amanda Braithwaite; Krista L. Scoggins; Edward J. Bilsky; Hamid I. Akbarali; William L. Dewey; Yan Zhang;
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1. 6β-N-Heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists [J] . YuanY., StevensD.L., BraithwaiteA., Bioorganic and Medicinal Chemistry Letters . 2012,第14期

机译：6β-N-杂环取代的纳丙胺衍生物午间作为潜在的导致外周Mu阿片受体选择性拮抗剂
2. 6β-N-Heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists [J] . YuanY., StevensD.L., BraithwaiteA., Bioorganic and Medicinal Chemistry Letters . 2012,第14a15期

机译：6β-N-杂环取代的纳曲胺衍生物NAP可能导致开发外周μ阿片受体选择性拮抗剂
3. 6β-N-Heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists [J] . YuanY., StevensD.L., BraithwaiteA., Bioorganic and Medicinal Chemistry Letters . 2012,第14a15期

机译：6β-N-杂环取代的纳曲胺衍生物NAP可能导致开发外周μ阿片受体选择性拮抗剂
4. Design and synthesis of bifunctional peptides:antagonists at CCKA/CCKB receptors and agonists as mu/delta opioid receptors [C] . Richard S.Agnes, Yeon Sun Lee, Peg Davis, the International Peptide Symposium . 2001

机译：双官能肽的设计与合成：Ccka / Cckb受体的拮抗剂和穆/δ阿片受体的激动剂
5. Promoting peripheral opioid analgesia: The role of interactions between mu- and delta-opioid receptor agonists. [D] . Schramm, Cicely L. 2010

机译：促进外周阿片类镇痛：mu和delta阿片类受体激动剂之间相互作用的作用。
6. 6β-N-Heterocyclic Substituted Naltrexamine Derivative NAP as a Potential Lead to Develop Peripheral Mu Opioid Receptor Selective Antagonists [O] . Yunyun Yuan, David L. Stevens, Amanda Braithwaite, -1

机译：6β-N-杂环取代的纳丙胺衍生物午间作为潜在的导致外周Mu阿片受体选择性拮抗剂
7. Design, Synthesis, and Biological Evaluation of 14-Heteroaromatic-Substituted Naltrexone Derivatives: Pharmacological Profile Switch from Mu Opioid Receptor Selectivity to Mu/Kappa Opioid Receptor Dual Selectivity [O] . Yunyun Yuan, Saheem A. Zaidi, Orgil Elbegdorj, 2013

机译：14-杂芳族取代的纳曲酮衍生物的设计，合成和生物学评价：来自Mu阿片受体的药理学剖面开关对亩/κ阿片类药物受体双重选择性的选择性

6β-N-Heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists

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