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A 13C-NMR study of the inhibition of papain by a dipeptide-glyoxal inhibitor.
Z-Phe-Ala-glyoxal (where Z is benzyloxycarbonyl) has been synthesized and shown to be a competitive inhibitor of papain with a K(i)=3.30+/-0.25 nM. (13)C-NMR has been used to show that in aqueous media, Z-Phe-[2-(13)C]Ala-glyoxal gives signals at 207.7 p.p.m. and 96.3 p.p.m. showing that both the al...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1222827/ https://ncbi.nlm.nih.gov/pubmed/12061892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20020499 |
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