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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LIAO, S., SHENDEROVICH, M. D., ZHANG, Z., MALETÍNSKÁ, L., SLANINOVÁ, J., 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. 1998, 120(29), 7393-7394. ISSN 0002-7863. E-ISSN 1520-5126.

Number of the records: 1