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Displacement of Estradiol from Estrogen Receptors by Simple Alkyl Phenols*

MUELLER, GERALD C., KIM, UH-HEE·1978·Endocrinology

Abstract

Simple alkyl phenols have been tested for their ability to prevent the binding of [3H]estradiol and to displace the prebound hormone from estrogen receptors of uterine cytosols. Tetrahydronaphthol, an analog of the A and B rings of estradiol, is highly effective in preventing the forward bindng of estradiol. p-sec-Amyl phenol (pSAP) with a flexible alkyl chain corresponding to the B ring of estradiol is highly effective at 0 C in displacing estradiol which had been prebound by the receptor. Both compounds were more effective at 0 C than at 23 C. The data are discussed in terms of sequential conformational changes which might be required for the binding and release of the natural hormones and their possible relevance to receptor action.

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Metadata

Authors
MUELLER, G. C., & KIM, U.-H.
Venue
Endocrinology
Published
1978-05
Volume
102
Issue
5
Pages
1429-1435
ISSN
  • 0013-7227 (ISSN-L)
  • 1945-7170
OpenAlex
W2125590866
Cited by
170
References
0
FWCI
0.86
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Displacement of Estradiol from Estrogen Receptors by Simple Alkyl Phenols*. https://app.cochat.ai/papers/10.1210/endo-102-5-1429
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MUELLER, G. C., & KIM, U.-H. (1978). Displacement of Estradiol from Estrogen Receptors by Simple Alkyl Phenols*. Endocrinology. https://doi.org/10.1210/endo-102-5-1429

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.