Substitution of the side-chain-constrained amino acids á-methyl-2',6'-dimethyl-4'-methoxytyrosine in position 2 of a bicyclic oxytoxin analogue provides unique insights into the bioactive topography of oxytocin antagonists

Name: Substitution of the side-chain-constrained amino acids á-methyl-2',6'-dimethyl-4'-methoxytyrosine in position 2 of a bicyclic oxytoxin analogue provides unique insights into the bioactive topography of oxytocin antagonists
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Liao, S.; Shenderovich, M. D.; Zhang, Z.; Maletínská, Lenka; Slaninová, Jiřina; Hruby, J. V.

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Substitution of the side-chain-constrained amino acids á-methyl-2',6'-dimethyl-4'-methoxytyrosine in position 2 of a bicyclic oxytoxin analogue provides unique insights into the bioactive topography of oxytocin antagonists

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0193105 - UOCHB-X 980133 RIV US eng J - Journal Article
Liao, S. - Shenderovich, M. D. - Zhang, Z. - Maletínská, Lenka - Slaninová, Jiřina - Hruby, J. V.
Substitution of the side-chain-constrained amino acids á-methyl-2',6'-dimethyl-4'-methoxytyrosine in position 2 of a bicyclic oxytoxin analogue provides unique insights into the bioactive topography of oxytocin antagonists.
Journal of the American Chemical Society. Roč. 120, č. 29 (1998), s. 7393-7394. ISSN 0002-7863. E-ISSN 1520-5126
Grant - others:Public Health Service(US) DK-17420
Subject RIV: CE - Biochemistry
Impact factor: 5.725, year: 1998
Permanent Link: http://hdl.handle.net/11104/0088819

Number of the records: 1