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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1994-7-19
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pubmed:abstractText |
The new decapeptide SB-75 (INN: Cetrorelix) has been characterized as a potent antagonist of luteinizing-hormone releasing hormone (LH-RH). Such derivatives are of great medicinal interest owing to their potential application in areas such as hormone-dependent tumors, uterine fibroids, and in diseases and conditions which result from inappropriate hormone levels or which can be treated by suppression of estrogens. SB-75 is the subject of intensive ongoing clinical evaluation and is an accepted standard for the design of new LH-RH antagonists. We characterized SB-75 by means of modern MS and NMR techniques to demonstrate the significance of both sequencing methods on a complicated unnatural decapeptide. Our structural elucidations with nuclear Overhauser (NOE) experiments revealed clear evidence for a highly flexible molecule with no single predominant conformation even in sodium dodecyl sulfate (SDS) mimicking a cellular membrane.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0367-8377
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
264-70
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8005749-Amino Acid Sequence,
pubmed-meshheading:8005749-Gonadotropin-Releasing Hormone,
pubmed-meshheading:8005749-Magnetic Resonance Spectroscopy,
pubmed-meshheading:8005749-Mass Spectrometry,
pubmed-meshheading:8005749-Molecular Sequence Data,
pubmed-meshheading:8005749-Protein Conformation,
pubmed-meshheading:8005749-Receptors, LHRH,
pubmed-meshheading:8005749-Solvents
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pubmed:year |
1994
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pubmed:articleTitle |
Structural investigation of Cetrorelix, a new potent and long-acting LH-RH antagonist.
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pubmed:affiliation |
Degussa AG, Hanau-Wolfgang, Germany.
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pubmed:publicationType |
Journal Article
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