Abstract
Very high affinity for opioid receptors (e.g., K(i)=0.052nM for mu) has been observed in the rationally designed naltrexone analogue 5. SAR and physical data supports the hypothesis that the 4-OH group of 5 stabilizes the 3-carboxamido group in the putative bioactive conformation.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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CHO Cells
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Cricetinae
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Humans
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Naltrexone / analogs & derivatives*
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Naltrexone / chemical synthesis
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Naltrexone / metabolism*
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Protein Binding / physiology
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Receptors, Opioid / metabolism*
Substances
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Receptors, Opioid
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Naltrexone