Luteinizing hormone-releasing hormone antagonists containing very hydrophobic amino acids
- 31 August 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 27 (9) , 1170-1174
- https://doi.org/10.1021/jm00375a015
Abstract
Note: In lieu of an abstract, this is the article's first page.This publication has 14 references indexed in Scilit:
- Synthesis and biological activity of some very hydrophobic superagonist analogs of luteinizing hormone-releasing hormoneJournal of Medicinal Chemistry, 1982
- PEPTIDE ANTAGONISTS OF LH-RH: LARGE INCREASES IN ANTIOVULATORY ACTIVITIES PRODUCED BY BASIC D-AMINO ACIDS IN THE SIX POSITIONEndocrinology, 1982
- A study of the applicability of QSAR calculation for peptide hormonesBiochemical and Biophysical Research Communications, 1981
- RADIOLIGAND ASSAY FOR GONADOTROPIN-RELEASING HORMONE - RELATIVE POTENCIES OF AGONISTS AND ANTAGONISTS1980
- New analogs of luliberin which inhibit ovulation in the ratBiochemical and Biophysical Research Communications, 1979
- An antiovulatory decapeptide of higher potency which has an -amino acid (Ac-Pro) in position 1Biochemical and Biophysical Research Communications, 1978
- Pituitary receptor binding activity of active, inactive, superactive and inhibitory analogs of gonadotropin-releasing hormoneBiochemical and Biophysical Research Communications, 1978
- [4‐Amino‐D‐phenylalanine6]luliberin. A biologically active abalog of the luteinizing hormone‐releasing factor suitable for affinity labelingBiopolymers, 1976
- An in Vivo Assay for Anti-LH-RH and Anti-FSH-RH Activity of Inhibitory Analogues of LH-RH∗Endocrinology, 1975
- Synthesis of 1-L-Penicillamine-oxytocin, 1-D-Penicillamine-oxytocin, and 1-Deaminopenicillamine-oxytocin, Potent Inhibitors of the Oxytocic Response of Oxytocin1Journal of Medicinal Chemistry, 1966