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Fmoc protected peptide mimetic based on a cyclohexane framework and incorporation into angiotensin II
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Medicinal Chemistry, Organic Pharmaceutical Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Medicinal Chemistry, Organic Pharmaceutical Chemistry.
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1997 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 53, no 37, 12497-12504 p.Article in journal (Refereed) Published
Abstract [en]

1,3,5-syn substituted cyclohexane based amino acids have been prepared and incorporated into synthetic peptides to serve as scaffold mimicking the Val-Tyr-Ile sequence of angiotensin II. The conformationally constrained tripeptide mimetic holds potential use as a γ-turn replacement.

Place, publisher, year, edition, pages
1997. Vol. 53, no 37, 12497-12504 p.
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Medical and Health Sciences
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URN: urn:nbn:se:uu:diva-51173DOI: 10.1016/S0040-4020(97)00779-5OAI: oai:DiVA.org:uu-51173DiVA: diva2:79082
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2017-12-04Bibliographically approved

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Gogoll, Adolf

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