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从不同角度看类固醇、类固醇领域以及优普强公司:创新概况

Steroids, the steroid community, and Upjohn in perspective: a profile of innovation.

作者信息

Hogg J A

机构信息

Experimental Sciences and Therapeutics, Upjohn Company, Kalamazoo, Michigan.

出版信息

Steroids. 1992 Dec;57(12):593-616. doi: 10.1016/0039-128x(92)90013-y.

Abstract

The announcement in 1949 at the Mayo Clinic of the dramatic effect of cortisone in alleviating the symptoms of rheumatoid arthritis triggered a competitive worldwide research and development effort directed toward a single goal, the practical synthesis of the rare corticosteroids. The confluence of an extraordinary coalescence of multiple events and circumstances in the growth of the Upjohn Company with the Mayo discovery, inclusive of a pioneering role in the steroid field, conspired to create an environment ripe for innovation. The breakthrough, which gave Upjohn an early competitive edge, followed with startling swiftness. A common mold of the genus Rhizopus was found to introduce enzymatically an 11 alpha-hydroxyl group directly into the female hormone progesterone, which had just been synthesized from the soybean sterol stigmasterol--a one-step solution to the known multistep alternatives for 11-oxygenation. Retrospective analysis of this event in perspective with other key developments before and after at Upjohn and in the steroid community reveals a striking profile of ongoing innovation. A parallel scenario in kind was repeated at Upjohn a quarter century later. The sister soybean sterol sitosterol was radically degraded microbiologically and concurrently oxygenated in ring C to produce 9 alpha-hydroxyandrostenedione, an alternative key intermediate for corticoid synthesis. New chemical processes, highly integrated with existing processes, assured the continuation of Upjohn's leading role in steroid hormone production.

摘要

1949年,梅奥诊所宣布可的松在缓解类风湿性关节炎症状方面具有显著效果,这引发了一场全球范围内的竞争性研发努力,目标只有一个,即实现稀有皮质类固醇的实际合成。在Upjohn公司的发展过程中,多种事件和情况的非凡融合,再加上在类固醇领域的开拓性作用,与梅奥诊所的这一发现共同营造了一个利于创新的成熟环境。Upjohn公司迅速取得了突破,获得了早期竞争优势。人们发现一种常见的根霉属霉菌能够通过酶促反应将11α-羟基直接引入刚刚由大豆甾醇豆甾醇合成的雌性激素孕酮中,这为已知的多步11-氧化替代方法提供了一步解决方案。从Upjohn公司以及类固醇领域前后的其他关键发展情况来回顾这一事件,可以发现持续创新的显著特征。四分之一世纪后,Upjohn公司又出现了类似的情况。大豆甾醇的姊妹甾醇谷甾醇通过微生物方法被彻底降解,同时在C环中被氧化,生成9α-羟基雄烯二酮,这是皮质激素合成的另一种关键中间体。与现有工艺高度整合的新化学工艺确保了Upjohn公司在类固醇激素生产中继续占据领先地位。

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