Prenylated flavonoids: Pharmacology and biotechnology

被引:275
作者
Botta, B
Vitali, A
Menendez, P
Misiti, D
Delle Monache, G
机构
[1] Univ Roma La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biologi, I-00185 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Ist Chim Riconoscimento Mol, I-00168 Rome, Italy
[3] Catedra Farmacognosia & Prod Nat, Fac Quim, Montevideo, Uruguay
关键词
D O I
10.2174/0929867053202241
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within the flavonoid class of natural products the prenylated sub-class is quite rich in structural variety and pharmacological activity. In the last twenty years a huge number of new structures has been reported, mostly from Leguminosae and Moraceae, with few coining from other genera. The presence, in different forms, of the isoprenoid chain can lead to impressive changes in biological activity, mostly attributed to an increased affinity for biological membranes and to an improved interaction with proteins. Molecules, such as xanthohumol and sophoraflavarione G, while being very structurally simple, show numerous pharmacological applications and are ideal candidates for SAR aimed to the discovery of new drugs.
引用
收藏
页码:713 / 739
页数:27
相关论文
共 155 条
[11]   Steroid transport, accumulation, and antagonism of P-glycoprotein in multidrug-resistant cells [J].
Barnes, KM ;
Dickstein, B ;
Cutler, GB ;
Fojo, T ;
Bates, SE .
BIOCHEMISTRY, 1996, 35 (15) :4820-4827
[12]   Prenyl flavonoids and membrane permeability [J].
Barron, D ;
Balland, C ;
Possety, F ;
Ravanel, P ;
Desfougeres, A .
ACTA BOTANICA GALLICA, 1996, 143 (06) :509-520
[13]   Isoprenylated flavonoids - A survey [J].
Barron, D ;
Ibrahim, RK .
PHYTOCHEMISTRY, 1996, 43 (05) :921-982
[14]   THE CLINICAL RELEVANCE OF MULTIDRUG RESISTANCE [J].
BELLAMY, WT ;
DALTON, WS ;
DORR, RT .
CANCER INVESTIGATION, 1990, 8 (05) :547-562
[15]   DIMETHYLALLYLPYROPHOSPHATE-3,9-DIHYDROXYPTEROCARPAN 10-DIMETHYLALLYL TRANSFERASE FROM PHASEOLUS-VULGARIS - IDENTIFICATION OF THE REACTION-PRODUCT AND PROPERTIES OF THE ENZYME [J].
BIGGS, DR ;
WELLE, R ;
VISSER, FR ;
GRISEBACH, H .
FEBS LETTERS, 1987, 220 (01) :223-226
[16]  
BOEDDEKER P, 1995, PHARM PHARM LETT, V5, P91
[17]   Synthesis and biological activity of 4-alkoxy chalcones: Potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance [J].
Bois, F ;
Boumendjel, A ;
Mariotte, AM ;
Conseil, G ;
Di Petro, A .
BIOORGANIC & MEDICINAL CHEMISTRY, 1999, 7 (12) :2691-2695
[18]   Recent advances in the discovery of flavonoids and analogs with high-affinity binding to P-glycoprotein responsible for cancer cell multidrug resistance [J].
Boumendjel, A ;
Di Pietro, A ;
Dumontet, C ;
Barron, D .
MEDICINAL RESEARCH REVIEWS, 2002, 22 (05) :512-529
[19]   B-ring substituted 5,7-dihydroxyflavonols with high-affinity binding to P-glycoprotein responsible for cell multidrug resistance [J].
Boumendjel, A ;
Bois, F ;
Beney, C ;
Mariotte, AM ;
Conseil, G ;
Di Pietro, A .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (01) :75-77
[20]  
BOURGESSEVENIER C, 2002, Patent No. 2002085393