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Structure−Activity Relationships of Bisphosphate Nucleotide Derivatives as P2Y1Receptor Antagonists and Partial Agonists

机译：二磷酸核苷酸衍生物作为p2Y（1）受体拮抗剂和部分激动剂的活性结构关系

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Erathodiyil Nandanan; Emidio Camaioni; Soo-Yeon Jang; Yong-Chul Kim; Gloria Cristalli; Piet Herdewijn; John A. Secrist; Kamal N. Tiwari; Arvind Mohanram; T. Kendall Harden; José L. Boyer; Kenneth A. Jacobson;
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年度 1999
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1. Structure-activity relationships of bisphosphate nucleotide derivatives as P2Y1 receptor antagonists and partial agonists. [J] . Nandanan E, Camaioni E, Jang SY, Journal of Medicinal Chemistry . 1999,第9期

机译：二磷酸核苷酸衍生物作为P2Y1受体拮抗剂和部分激动剂的构效关系。
2. 2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with selective affinity for the 5-HT(4) receptor: synthesis and structure-affinity and structure-activity relationships of a new series of partial agonist and antagonist derivatives. [J] . Tapia I, Alonso Cires-L, Lopez Tudanca-PL, Journal of Medicinal Chemistry . 1999,第15期

机译：对5-HT（4）受体具有选择性亲和力的2,3-二氢-2-羰基-1H-苯并咪唑-1-羧酰胺：一系列新的部分激动剂和拮抗剂衍生物的合成，结构亲和力和结构活性关系。
3. Structure-activity relationships of peptides incorporating a bioactive reverse-turn heterocycle at the melanocortin receptors: Identification of a 5800-fold mouse melanocortin-3 receptor (mMC3R) selective antagonist/partial agonist versus the mouse melanocortin-4 receptor (mMC4R) [J] . Singh A., Dirain M., Witek R., Journal of Medicinal Chemistry . 2013,第7期

机译：在黑皮质素受体上结合有生物活性反向杂环的肽的结构活性关系：鉴定5800倍小鼠黑皮质素-3受体（mMC3R）选择性拮抗剂/部分激动剂对小鼠黑皮质素4受体（mMC4R）
4. Synthesis and pharmacological activity of Dmt-Tic analogs with highly potent agonist and antagonist/agonist opioid activity [C] . Remo Guerrini, Gianfranco Balboni, Daniela Girolamo Calo, the International Peptide Symposium . 2001

机译：具有高效激动剂和拮抗剂/激动剂阿片类能活性DMT-TIC类似物的合成与药理活性
5. Selective GLP-1 receptor antagonists and glucagon/GLP-1 co-agonists discovered through an investigation into the structure-activity relationship in glucagon-related peptides. [D] . Patterson, James T. 2011

机译：通过研究胰高血糖素相关肽的结构-活性关系，发现了选择性的GLP-1受体拮抗剂和胰高血糖素/ GLP-1共激动剂。
6. Structure-Activity Relationships of Bisphosphate Nucleotide Derivatives as P2Y1 Receptor Antagonists and Partial Agonists [O] . Erathodiyil Nandanan, Emidio Camaioni, Soo-Yeon Jang, -1

机译：双磷酸核苷酸衍生物作为P2Y1受体拮抗剂和部分激动剂的结构-活性关系。
7. Synthesis and Structure-Activity Relationships of Uracil Nucleotide Derivatives and Analogues as Agonists at Human P2Y2, P2Y4, and P2Y6 Receptors [O] . -1

机译：尿嘧啶核苷酸衍生物和类似物作为人P2Y2，P2Y4和P2Y6受体的激动剂的合成和结构 - 活性关系

Structure−Activity Relationships of Bisphosphate Nucleotide Derivatives as P2Y1Receptor Antagonists and Partial Agonists

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