An. Nurfina et al., SYNTHESIS OF SOME SYMMETRICAL CURCUMIN DERIVATIVES AND THEIR ANTIINFLAMMATORY ACTIVITY, European journal of medicinal chemistry, 32(4), 1997, pp. 321-328
Curcumin is not only a frequently used food additive, but it is also a
well-known constituent of Indonesian traditional medicines. Several b
eneficial effects are ascribed to curcumin, eg, its antiinflammatory p
roperties. In order to study the antiinflammatory activity, a series o
f curcumin derivatives were prepared and the inhibition of the carrage
enin-induced oedema by these compounds was established. It appeared th
at the pam hydroxy groups in curcumin are important for antiinflammato
ry activity. This activity is enhanced when, in combination with the p
ara hydroxy groups, the meta positions are occupied with alkyl groups.
Since the methyl derivatives are more active than the corresponding e
thyl and tert-butyl derivatives, it is suggested that sterical hindran
ce is involved.