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用于DNA的新型单功能试剂作为银屑病光化学疗法的可能药物:4,5'-二甲基白芷素的衍生物

New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin.

作者信息

Dall'Acqua F, Vedaldi D, Caffieri S, Guiotto A, Rodighiero P, Baccichetti F, Carlassare F, Bordin F

出版信息

J Med Chem. 1981 Feb;24(2):178-84. doi: 10.1021/jm00134a010.

Abstract

With the aim of obtaining new agents for the photochemotherapy of psoriasis, we have prepared monofunctional reagents for DNA by starting from 4,5'-dimethylangelicin (2), an angular furocoumarin, and introducing in a 4'-(hydroxymethyl) (3), 4'-(methoxymethyl) (4), or 4'-(aminomethyl) group (5), in way analogous to what other authors have done previously on trioxsalen, a DNA bifunctional reagent. These new compounds form complexes with DNA in the ground state and by successive irradiation (UV-A) undergo monofunctional photoaddition to the macromolecule. Photobinding to DNA was highest for 3 and gradually lower for 4 and 5, respectively. These compounds do not form interstrand photocross-linkages in DNA and do not show any skin phototoxicity. Fluorimetric studies show that their 4',5' double bond is involved in the photoaddition to DNA. Their photobiological activity evaluated on Ehrlich ascites tumor cells and on T2 phages was strictly connected with their photobinding to DNA. The effect of the introduction of hydroxymethyl and methoxymethyl groups in angular 2 is somewhat similar to that previously described for trioxsalen: the introduction of an aminomethyl group in 2 markedly increases the affinity in the dark for DNA but under UV-A irradiation strongly inhibits photobinding to the macromolecule. By contrast, in the analogous derivative of trioxsalen both the affinity for DNA in the dark and the photobinding to DNA increased.

摘要

为了获得用于银屑病光化学疗法的新试剂,我们从角型呋喃香豆素4,5'-二甲基白芷素(2)出发,以类似于其他作者先前对DNA双功能试剂三氧沙林所做的方式,引入4'-(羟甲基)(3)、4'-(甲氧基甲基)(4)或4'-(氨甲基)基团(5),制备了用于DNA的单功能试剂。这些新化合物在基态下与DNA形成复合物,并通过连续照射(UV-A)对大分子进行单功能光加成。3与DNA的光结合最高,4和5的光结合则分别逐渐降低。这些化合物不会在DNA中形成链间光交联,也不显示任何皮肤光毒性。荧光研究表明,它们的4',5'双键参与了与DNA的光加成。在艾氏腹水瘤细胞和T2噬菌体上评估的它们的光生物活性与它们与DNA的光结合密切相关。在角型2中引入羟甲基和甲氧基甲基基团的效果与先前描述的三氧沙林有些相似:在2中引入氨甲基基团显著增加了在黑暗中对DNA的亲和力,但在UV-A照射下强烈抑制与大分子的光结合。相比之下,在三氧沙林的类似衍生物中,在黑暗中对DNA的亲和力和与DNA的光结合都增加了。

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