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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1998-5-1
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pubmed:abstractText |
One unsubstituted and one stereoselectively prepared 3-(S)-substituted-2-oxopiperazine have been used as dipeptide templates to generate tetrapeptide analogues. NMR analysis shows that these tetrapeptide analogues present an inverse gamma-turn conformation in chloroform.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1397-002X
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
116-20
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9516046-Alkylation,
pubmed-meshheading:9516046-Chloroform,
pubmed-meshheading:9516046-Dipeptides,
pubmed-meshheading:9516046-Hydrogen Bonding,
pubmed-meshheading:9516046-Magnetic Resonance Spectroscopy,
pubmed-meshheading:9516046-Mass Spectrometry,
pubmed-meshheading:9516046-Molecular Structure,
pubmed-meshheading:9516046-Oligopeptides,
pubmed-meshheading:9516046-Piperazines,
pubmed-meshheading:9516046-Protein Conformation,
pubmed-meshheading:9516046-Templates, Genetic
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pubmed:year |
1998
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pubmed:articleTitle |
Synthesis and conformational analysis of two 2-oxopiperazine-containing tetrapeptide analogues.
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pubmed:affiliation |
Laboratoire de Chimie Thérapeutique, Faculté des Sciences Pharmaceutiques et Biologiques, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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