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Interactions of befunolol, a beta-adrenergic partial agonist, and its derivatives with high and low affinity sites in beta-adrenoceptors.

机译：Befunolol，β-肾上腺素能部分激动剂及其衍生物在β-肾上腺素受体中具有高和低亲和力点的衍生物的相互作用。

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KATSUO KOIKE; ISSEI TAKAYANAGI;
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年度 1987
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1. A Beta-Adrenergic Partial Agonist (Befunolol) Discriminates Two Different Affinity Sites [J] . Issei TAKAYANAGI, Katsuo KOIKE Japanese Journal of Pharmacology . 1986,第2期

机译：β-肾上腺素部分激动剂（贝芬洛尔）区分两个不同的亲和力站点。
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. 11 beta-alkyl-Delta(9)-19-nortestosterone derivatives: High-affinity ligands and potent partial agonists of the androgen receptor [J] . Muddana SS, Price AM, MacBride MM, Journal of Medicinal Chemistry . 2004,第21期

机译：11β-烷基-Delta（9）-19-睾丸激素衍生物：雄激素受体的高亲和力配体和强效部分激动剂
4. GENERALIZED CONCENTRATION ADDITION MODEL PREDICTS INTERACTIONS OF TCDD WITH PARTIAL AGONIST AhR LIGANDS [C] . Gregory J.Howard, Jennifer J.Schlezinger, Thomas F.Webster American Chemical Society National Meeting . 2007

机译：广义浓度添加模型预测TCDD与部分激动剂AHR配体的相互作用
5. Studies on the Survival of Ovarian Cancer Cells Following Treatment with Beta-Adrenergic Receptor Agonists and Antagonists [D] . Horan, Noah Patrick. 2020

机译：用β-肾上腺素能受体激动剂和拮抗剂治疗卵巢癌细胞存活的研究
6. Site-directed mutagenesis of human beta-adrenergic receptors: substitution of aspartic acid-130 by asparagine produces a receptor with high-affinity agonist binding that is uncoupled from adenylate cyclase. [O] . C M Fraser, F Z Chung, C D Wang, 1988

机译：人β-肾上腺素受体的定点诱变：天冬酰胺取代天冬氨酸130产生具有高亲和力激动剂结合的受体该受体与腺苷酸环化酶脱钩。
7. Site-directed mutagenesis of human beta-adrenergic receptors: substitution of aspartic acid-130 by asparagine produces a receptor with high-affinity agonist binding that is uncoupled from adenylate cyclase. [O] . Fraser, C M, Chung, F Z, Wang, C D, 1988

机译：人β-肾上腺素受体的定点诱变：天冬酰胺取代天冬氨酸130产生具有高亲和力激动剂结合的受体，该受体与腺苷酸环化酶脱钩。
8. Short-Term Desensitization of Muscarinic Cholinergic Receptors in Mouse Neuroblastoma Cells: Selective Loss of Agonist Low-Affinity and Pirenzepine High-Affinity Binding Sites [R] . Cioffi, C. L., El-Fakahany, E. E. 1986

机译：小鼠神经母细胞瘤细胞中毒蕈碱胆碱能受体的短期脱敏：激动剂低亲和力和哌仑西平高亲和力结合位点的选择性丧失

Interactions of befunolol, a beta-adrenergic partial agonist, and its derivatives with high and low affinity sites in beta-adrenoceptors.

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