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作为新型大麻素受体配体的 BAY 59-3074 的构象限制类似物。

Conformationally constrained analogs of BAY 59-3074 as novel cannabinoid receptor ligands.

机构信息

Center for Drug Discovery, 116 Mugar Life Sciences Building, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, United States.

出版信息

Bioorg Med Chem Lett. 2011 Oct 1;21(19):5999-6002. doi: 10.1016/j.bmcl.2011.07.017. Epub 2011 Jul 23.

DOI:10.1016/j.bmcl.2011.07.017
PMID:21880487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3693451/
Abstract

To obtain information on the pharmacophoric requirements of the CB1/CB2 partial agonist BAY 59-3074 we have synthesized a series of new conformationally constrained dibenzofuran (4a-d) and dibenzopyran analogs (5). All constrained analogs exhibited reduced binding affinity at both cannabinoid receptor subtypes, suggesting that planar conformations of these ligands are less favored by both receptors. We also found that 4c, 4d, and 5 exhibited 3- to 12-fold selectivity for hCB2 over rCB1 receptors and may serve as new chemotypes for the development of CB2-selective cannabinergics.

摘要

为了获取 CB1/CB2 部分激动剂 BAY 59-3074 的药效团需求信息,我们合成了一系列新的刚性二苯并呋喃(4a-d)和二苯并吡喃类似物(5)。所有的刚性类似物在两种大麻素受体亚型上的结合亲和力都降低了,这表明这些配体的平面构象对两种受体的亲和力都较低。我们还发现 4c、4d 和 5 对 hCB2 受体相对于 rCB1 受体具有 3 至 12 倍的选择性,它们可能成为开发 CB2 选择性大麻素受体激动剂的新型化学型。

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本文引用的文献

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Latest advances in cannabinoid receptor agonists.大麻素受体激动剂的最新进展。
Expert Opin Ther Pat. 2009 Dec;19(12):1647-73. doi: 10.1517/13543770903436505.
2
Emerging strategies for exploiting cannabinoid receptor agonists as medicines.将大麻素受体激动剂开发为药物的新兴策略。
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Emerging role of the cannabinoid receptor CB2 in immune regulation: therapeutic prospects for neuroinflammation.大麻素受体CB2在免疫调节中的新作用:神经炎症的治疗前景
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Should peripheral CB(1) cannabinoid receptors be selectively targeted for therapeutic gain?外周CB(1)大麻素受体是否应被选择性靶向以获得治疗益处?
Trends Pharmacol Sci. 2009 Jan;30(1):1-7. doi: 10.1016/j.tips.2008.10.001. Epub 2008 Nov 29.
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Cannabilactones: a novel class of CB2 selective agonists with peripheral analgesic activity.大麻内酯:一类具有外周镇痛活性的新型CB2选择性激动剂。
J Med Chem. 2007 Dec 27;50(26):6493-500. doi: 10.1021/jm070441u. Epub 2007 Nov 27.
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Cannabinoid CB2 receptors: a therapeutic target for the treatment of inflammatory and neuropathic pain.大麻素CB2受体:治疗炎症性和神经性疼痛的治疗靶点。
Br J Pharmacol. 2008 Jan;153(2):319-34. doi: 10.1038/sj.bjp.0707531. Epub 2007 Nov 12.
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The endocannabinoid system as an emerging target of pharmacotherapy.内源性大麻素系统作为药物治疗的一个新兴靶点。
Pharmacol Rev. 2006 Sep;58(3):389-462. doi: 10.1124/pr.58.3.2.
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Identification and functional characterization of brainstem cannabinoid CB2 receptors.脑干大麻素CB2受体的鉴定与功能表征
Science. 2005 Oct 14;310(5746):329-32. doi: 10.1126/science.1115740.
9
Discriminative stimulus effects of the structurally novel cannabinoid CB1/CB2 receptor partial agonist BAY 59-3074 in the rat.结构新颖的大麻素CB1/CB2受体部分激动剂BAY 59-3074对大鼠的辨别性刺激作用。
Eur J Pharmacol. 2004 Nov 28;505(1-3):127-33. doi: 10.1016/j.ejphar.2004.10.012.
10
3-[2-cyano-3-(trifluoromethyl)phenoxy]phenyl-4,4,4-trifluoro-1-butanesulfonate (BAY 59-3074): a novel cannabinoid Cb1/Cb2 receptor partial agonist with antihyperalgesic and antiallodynic effects.3-[2-氰基-3-(三氟甲基)苯氧基]苯基-4,4,4-三氟-1-丁烷磺酸盐(BAY 59-3074):一种具有抗痛觉过敏和抗异常性疼痛作用的新型大麻素Cb1/Cb2受体部分激动剂。
J Pharmacol Exp Ther. 2004 Aug;310(2):620-32. doi: 10.1124/jpet.103.062836. Epub 2004 May 12.