Solid-phase synthesis of 16 potent (selective and nonselective) in vivo antagonists of oxytocin
- 1 February 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 32 (2) , 382-391
- https://doi.org/10.1021/jm00122a016
Abstract
Note: In lieu of an abstract, this is the article's first page.This publication has 20 references indexed in Scilit:
- DESIGN AND SYNTHESIS OF POTENT IN VIVO ANTAGONISTS OF OXYTOCINInternational Journal of Peptide and Protein Research, 1980
- [1-(.beta.-mercapto-.beta.,.beta.-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine]arginine-vasopressin and [1-(.beta.-mercapto-.beta.,.beta.-cyclopentamethylenepropionic acid)]arginine-vasopressin, two highly potent antagonists of the vasopressor response to arginine-vasopressinJournal of Medicinal Chemistry, 1980
- The Design of Effectivein VivoAntagonists of Rat Uterus and Milk Ejection Responses to Oxytocin*Endocrinology, 1980
- Synthetic antagonists of in vivo responses by the rat uterus to oxytocinJournal of Medicinal Chemistry, 1979
- [1-Deaminopenicillamine,4-threonine]oxytocin, a potent inhibitor of oxytocinJournal of Medicinal Chemistry, 1978
- 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
- Solid-Phase Peptide Synthesis. III. An Improved Synthesis of Bradykinin*Biochemistry, 1964
- A Highly Potent Analogue of Oxytocin, Desamino-oxytocinJournal of Biological Chemistry, 1962
- EFFECT OF MAGNESIUM ION ON THE RESPONSE OF THE RAT UTERUS TO NEUROHYPOPHYSIAL HORMONES AND ANALOGUES1Endocrinology, 1960
- DIFFERENCES IN THE ANTIDIURETIC RESPONSES OF RATS TO THE INTRAVENOUS ADMINISTRATIONOF LYSINE AND ARGININE VASOPRESSINS1Endocrinology, 1958