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- W2034298924 abstract "In the present research, chitooligosaccharides (COS) with molecular weight 800–3000 Da and 90% of deacetylation were chemically modified by grafting 2-chloroethylamino hydrochloride at C-6 position to synthesize angiotensin I converting enzyme (ACE) inhibitory chitin derivatives based on the properties of ACE inhibitors. The synthetic product was designated as aminoethyl chitooligosaccharide (AE-COS) with molecular weight 800.79–4765 Da. Its IC50 value on ACE was 0.8017 μg/mL. Furthermore, Lineweaver-Burk plots revealed that the inhibition was competitive via obligatory binding site of ACE. Therefore, these results exhibited that substitution of the hydrogen atom at the C-6 position of pyranose residue by the aminoethyl group promotes ACE inhibitory effects of COS." @default.
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- W2034298924 date "2008-01-01" @default.
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- W2034298924 title "Aminoethyl chitooligosaccharides inhibit the activity of angiotensin converting enzyme" @default.
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- W2034298924 doi "https://doi.org/10.1016/j.procbio.2007.10.018" @default.
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