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100
124
OH
C17
+
HO
CH 2
HH
OH
%
+
HO
123
137
348
166
0
m/z
0
100
200
300
400
500
C19
124
100
OH
+
HO
CH 2
HH
OH
%
+
HO
123
137
376
166
0
m/z
0
100
200
300
400
500
C25
100
124
OH
+
HO
CH 2
OH
HH
%
+
HO
123
137
166
460
0
m/z
0
100
200
300
400
500
Fig. 10.6. Mass spectra of 5-n-alkylresorcinols homologues differing in the length of the alkyl chain.
The typical fragmentation pattern is observed, including the base fragment at m / z 124 (McLafferty
rearrangement of the phenolic ring) and fragments at m / z 123 (dihydroxytropylium ion).
10.7.2
Effects on proteins
hydrophobic regions of the proteins, par-
ticularly near tryptophan residues (Sikorski
et al., 1987). Another possibility could be
the incorporation of ARs to a biological
membrane, which can decrease the lipid
ARs are able to inhibit the activity of sev-
eral enzymes. This effect may be mediated
by direct binding of these compounds to the
 
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