SYNTHESIS OF SOME SYMMETRICAL CURCUMIN DERIVATIVES AND THEIR ANTIINFLAMMATORY ACTIVITY

Citation
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
Citations number
15
Categorie Soggetti
Chemistry Medicinal
ISSN journal
02235234
Volume
32
Issue
4
Year of publication
1997
Pages
321 - 328
Database
ISI
SICI code
0223-5234(1997)32:4<321:SOSSCD>2.0.ZU;2-5
Abstract
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.