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6-氧代-N-环丙基甲基吗啡喃类化合物20681-S和20682-S作为麻醉性拮抗镇痛药的药理学研究

The pharmacology of 20681-S and 20682-S, 6-oxo-N-cyclopropylmethylmorphinans, as narcotic antagonist analgesics.

作者信息

Hirose K, Matsushita A, Kojima Y, Eigyo M, Jyoyama H, Shiomi T, Tsukinoki Y, Hatakeyama H, Matsubara K, Kawasaki K

出版信息

Arch Int Pharmacodyn Ther. 1979 Sep;241(1):79-91.

PMID:43119
Abstract

It has been demonstrated that L-3hydroxy-6-oxo-N-cyclopropylmethylmorphinan methansulfonate (20681-S) and L-3,14-dihydroxy-6-oxo-N-cyclopropylmethylmorphinan methansulfonate (20682-S), have antinociceptive and narcotic antagonistic properties. In the rodent antinociceptive test, the action of 20681-S was more potent and of longer duration than that of morphine and of cyclazocine after subcutaneous or oral administration. The antinociceptive effect of 20682-S ranked between that of morphine and that of pentazocine in the mouse acetic acid-writhing test. Both compounds possessed potent narcotic antagonistic activities, 20682-S being more active than naloxone and oxilorphan and 20681-S being equipotent with cyclazocine. The latent side effects (respiratory depression and fall in blood pressure) and the acute toxicity of 20681-S and 20682-S, were less than those of reference narcotic antagonists or of narcotic antagonist analgesics.

摘要

已证明L-3-羟基-6-氧代-N-环丙基甲基吗啡烷甲磺酸盐(20681-S)和L-3,14-二羟基-6-氧代-N-环丙基甲基吗啡烷甲磺酸盐(20682-S)具有抗伤害感受和麻醉拮抗特性。在啮齿动物抗伤害感受试验中,皮下或口服给药后,20681-S的作用比吗啡和环唑辛更强且持续时间更长。在小鼠醋酸扭体试验中,20682-S的抗伤害感受作用介于吗啡和喷他佐辛之间。两种化合物均具有强效的麻醉拮抗活性,20682-S比纳洛酮和氧吗啡酮更具活性,20681-S与环唑辛等效。20681-S和20682-S的潜在副作用(呼吸抑制和血压下降)以及急性毒性均低于参考麻醉拮抗剂或麻醉拮抗镇痛药。

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