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Figure 3.8 Chemical structures for amylase inhibitors, compounds 57-59, 5-caffeoyl
quinic acid, and 4,5-dicaffeoyl quinic acid.
using DNSA assay to be 10 times (EC 50 of
2.0 m M) stronger than aca-
rbose (EC 50 of 19 m M). Such a high activity is quite rarely seen in poly-
phenolic compounds and warrants further investigation particularly on
its inhibition mechanism and selectivity when these compounds are chal-
lenged with complex food matrix. Myricetin is a strong radical scavenger
and thus the stability of
is also a concern. The authors reported
that quercetin had comparable EC 50 (17 m M) as that of acarbose (19 m M).
Using the turbidity assay we developed in our lab, we could not detect any
inhibition activity of quercetin against pancreatic a -amylase using acarbose
as the reference standard (Huang et al., unpublished results). Therefore, it
needs to be verified if the EC 50 reported is method dependent to rule out
potential artifact ( Manaharan et al., 2012 ) . Cleistocalyx operculatus also
9
and
10
 
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