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Mixed μ agonist/ δ antagonist opioid analgesics with reduced tolerance liabilities and uses thereof

机译:具有降低的耐受性的混合μ激动剂/δ拮抗剂阿片类镇痛药及其用途

摘要

An opioid narcotics used for the treatment of moderate-to-severe pain that primarily exert their analgesic effects through μ receptors. Although, traditional μ agonists can cause undesired side effects, including tolerance, addition of δ antagonists can attenuate said side effects. The present invention includes 4a,9-dihydroxy-7a-(hydroxymethyl)-3-methyl-2,3,4,4a,5,6-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7(7aH)-one (UMB 425) a 5,14-bridged morphinan-based orvinol precursor, along with analogs of morphine, dihydromorphine, hydromorphone, codeine, dihydrocodeine, hydrocodone and ethylmorphine. Although UMB 425 lacks δ-specific motifs, conformationally sampled pharmacophore models for μ and δ receptors predict it to have efficacy similar to morphine at μ receptors and similar to naltrexone at δ receptors, due to the compound sampling conformations in which the hydroxyl moiety interacts with the receptors similar to orvinols. UMB 425 exhibits a mixed μ agonist/δ antagonist profile as determined in receptor binding. UMB 425 has mixed μ agonist/δ antagonist properties in vitro that translate to reduced tolerance liabilities in vivo.
机译:阿片类药物,用于治疗中度至重度疼痛,主要通过μ受体发挥镇痛作用。尽管传统的μ受体激动剂会引起不良反应,包括耐受性,但添加δ拮抗剂可以减轻上述副作用。本发明包括4a,9-二羟基-7a-(羟甲基)-3-甲基-2,3,4,4a,5,6-六氢-1H-4,12-甲基苯并呋喃[3,2-e]异喹啉- 7(7aH)-一(UMB 425)一种5,14桥联的吗啡喃基酚乙烯基前体,以及吗啡,二氢吗啡,氢吗啡酮,可待因,二氢可待因,氢可酮和乙基吗啡的类似物。尽管UMB 425缺少δ特异性基元,但由于μ和δ受体的构象采样药效团模型预测,与羟基受体上的吗啡相似,在δ受体上具有类似于纳曲酮的功效,这是由于羟基部分与之相互作用的化合物采样构象受体与酚醛树脂相似。如在受体结合中所确定的,UMB 425展现出混合的μ激动剂/δ拮抗剂特性。 UMB 425在体外具有混合的μ激动剂/δ拮抗剂特性,从而降低了体内的耐受性。

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