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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
Proc R Soc Med. 1974 January; 67(1): 41–42.
PMCID: PMC1645685

Pharmacology of hydroxy-analogues of oxytocin.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Dean CR, Hope DB. The isolation of neurophysin-I and-II from bovine pituitary neurosecretory granules separated on a large scale from other subcellular organelles. Demonstration of slow equilibration of neurosecretory granules during centrifugation in a sucrose density gradient. Biochem J. 1968 Jan;106(2):565–573. [PubMed]
  • Ferrier BM, Jarvis D, Du Vigneaud V. Deamino-oxytocin. Its isolation by partition chromatography on Sephadex and crystallization from water, and its biological activities. J Biol Chem. 1965 Nov;240(11):4264–4266. [PubMed]
  • HOPE DB, MURTI VV, DU VIGNEAUD V. A highly potent analogue of oxytocin, desamino-oxytocin. J Biol Chem. 1962 May;237:1563–1566. [PubMed]
  • Hope DB, Wälti M. (1-(1-2-Hydroxy-3-mercaptopropanoic acid))-oxytocin, a highly potent analogue of oytocin not bound by neurophysin. Biochem J. 1971 Dec;125(3):909–911. [PubMed]
  • Manning M, Coy E, Sawyer WH. Solid-phase synthesis of (4-threonine)-oxytocin. A more potent and specific oxytocic agent than oxytocin. Biochemistry. 1970 Sep 29;9(20):3925–3930. [PubMed]
  • PFEIFFER CC. Optical isomerism and pharmacological action, a generalization. Science. 1956 Jul 6;124(3210):29–31. [PubMed]
  • Wälti M, Hope DB. Synthesis of (1-(L-2-hydroxy-3-mercaptopropanoic acid))oxytocin, a highly potent analogue of oxytocin. J Chem Soc Perkin 1. 1972;15:1946–1950. [PubMed]
  • Yamashiro D, Gillessen D, Du Vigneaud V. Simultaneous synthesis of 1-hemi-D-cystine-oxytocin and oxytocin and separation of the diastereoisomers by partition chromatography on sephadex and by countercurrent distribution. J Am Chem Soc. 1966 Mar 20;88(6):1310–1313. [PubMed]

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