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Understanding the structural requirements of 4-anilidopiperidine analogues for biological activities at μ and δ opioid receptors
New 4-anilidopiperidine analogues in which the phenethyl group of fentanyl was replaced by several aromatic ring-contained amino acids (or acids) were synthesized to study the biological effect of the substituents on μ and δ opioid receptor interactions. These analogues showed broad (47 nM–76 μM) bu...
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| Hlavní autoři: | , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2007
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2274923/ https://ncbi.nlm.nih.gov/pubmed/17329100 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2007.01.114 |
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