3-(ALPHA, ALPHA-DIMETHYLALLYL)-PSORALEN - LINEAR FUROCOUMARIN FORMING MAINLY 4',5'-MONOFUNCTIONAL ADDUCTS WITH DNA

被引:22
作者
VEDALDI, D [1 ]
DALLACQUA, F [1 ]
CAFFIERI, S [1 ]
RODIGHIERO, G [1 ]
机构
[1] UNIV PADUA, INST PHARMACEUT CHEM, CNR, CTR STUDIO CHIM FARM & PRODOTTI BIOLOGICAMENTE ATT, I-35100 PADUA, ITALY
关键词
D O I
10.1111/j.1751-1097.1979.tb07049.x
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
Abstract— 3‐(α,αdimethylallyl)‐psoralen, a furocoumarin derivative recently isolated from Hortia arborea. has been studied with regard to its photoreacting (365 nm) capacity with native DNA. This compound photobinds to DNA to a much lower extent than psoralen, forming mainly 4.5′‐monofunc‐tional adducts, due to the presence in the 3‐position of α.α‐dimethylallyl group. which exerts a considerable hindrance both for the formation of a molecular complex with native DNA and for the photoreaction of the3,4‐double bond. This site of the molecule photoreacts, and, only 2.5% of the bound substance forms cross‐linkages. Therefore. 3‐(α,α‐dimethylallyl).psoralen behaves as a fairly pure mono‐functional reagent. Copyright © 1979, Wiley Blackwell. All rights reserved
引用
收藏
页码:277 / 281
页数:5
相关论文
共 25 条
[1]  
[Anonymous], [No title captured]
[2]   STRUCTURAL SPECIFICITY IN LETHAL AND MUTAGENIC ACTIVITY OF FUROCOUMARINS IN YEAST-CELLS [J].
AVERBECK, D ;
CHANDRA, P ;
BISWAS, RK .
RADIATION AND ENVIRONMENTAL BIOPHYSICS, 1975, 12 (03) :241-252
[3]  
AVERBECK D, 1976, 7 INT C PHOT ROM, P137
[4]  
BACCICHETTI F, 1976, Z NATURFORSCH C, V31, P207
[5]  
BORDIN F, 1975, ITAL J BIOCHEM, V24, P258
[7]   FLUORIMETRIC DETERMINATION OF 4',5'-CYCLOADDUCTS IN DNA-PSORALEN PHOTOREACTION [J].
DALLACQUA, F ;
CAFFIERI, S ;
RODIGHIERO, G .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1978, 27 (01) :77-79
[8]  
DALLACQUA F, 1971, Z NATURFORSCH PT B, VB 26, P561
[9]  
DALLACQUA F, 1974, Z NATURFORSCH C, VC 29, P635
[10]  
DALLACQUA F, 1977, RES PHOTOBIOLOGY, P245