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雷洛昔芬:一种具有多靶点系统效应的选择性雌激素受体调节剂(SERM)。

Raloxifene: A selective estrogen receptor modulator (SERM) with multiple target system effects.

作者信息

Muchmore D B

机构信息

Lilly Research Laboratories, Indianapolis, Indiana, USA.

出版信息

Oncologist. 2000;5(5):388-92. doi: 10.1634/theoncologist.5-5-388.

Abstract

Selective estrogen receptor modulators (SERMs) exhibit a pharmacologic profile characterized by estrogen agonist activity in some tissues with estrogen antagonist activity in other tissues. These compounds were initially called "antiestrogens," but it was subsequently recognized that this inadequately described their spectrum of activities. The first widely used SERM, tamoxifen, has estrogen antagonist activity in breast tissue but shows estrogen-like activity in other tissues. Raloxifene is another SERM in clinical use, and it was developed to avoid some of the undesirable estrogen agonist actions of other SERMs to improve the drug safety profile. Raloxifene has been introduced for clinical use in treatment and prevention of postmenopausal osteoporosis. This review will explore the preclinical and clinical pharmacology of raloxifene, and compare it to other SERMs currently available for clinical use.

摘要

选择性雌激素受体调节剂(SERM)具有一种药理学特性,其特点是在某些组织中表现出雌激素激动剂活性,而在其他组织中表现出雌激素拮抗剂活性。这些化合物最初被称为“抗雌激素”,但后来人们认识到这并不能充分描述它们的活性谱。第一种广泛使用的SERM他莫昔芬,在乳腺组织中具有雌激素拮抗剂活性,但在其他组织中表现出雌激素样活性。雷洛昔芬是另一种临床使用的SERM,它的研发是为了避免其他SERM一些不良的雌激素激动剂作用,以改善药物安全性。雷洛昔芬已被引入临床用于治疗和预防绝经后骨质疏松症。本综述将探讨雷洛昔芬的临床前和临床药理学,并将其与目前临床使用的其他SERM进行比较。

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