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Luteinizing Hormone-releasing Hormone Antagonists in Gynecology

  • J. B. Engel
  • K. Diedrich
Conference paper

Abstract

The elucidation of the structure of LHRH in 1971 (Serially et al., 1971), a major breakthrough in endocrinology, was soon followed by the synthesis of LHRH superagonists (Karten and Rivier, 1986), which were more stable to cleavage and showed greater affinity to the LHRH receptor, mainly through amino acid substitutions at positions 6 and 10 of the native LHRH (Koch et al., 1977). These analogs were originally synthesized to mimic the action of LHRH but it was soon discovered that the compounds, after a flare-up of FSH and LH, led to pharmacological hypophysectomy via LHRH receptor depletion of the pituitary (Emons and Schally, 1994).

Keywords

Luteinizing Hormone Ovarian Stimulation Uterine Fibroid GnRH Antagonist LHRH Agonist 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Italia 2003

Authors and Affiliations

  • J. B. Engel
  • K. Diedrich

There are no affiliations available

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