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通过 BGLation 合成高水溶性贝特衍生物。

Synthesis of highly water-soluble fibrate derivatives via BGLation.

机构信息

Department of Pharmaceutical Chemistry, Institute of Health Biosciences, Graduate School of The University of Tokushima, Tokushima, Japan.

出版信息

Bioorg Med Chem Lett. 2012 Oct 15;22(20):6425-8. doi: 10.1016/j.bmcl.2012.08.057. Epub 2012 Aug 23.

Abstract

Three water-soluble fibrates (fenofibrate, bezafibrate and chlofibrate) conjugated with a symmetrically branched glyceryl trimer (BGL003) were synthesized, and an evaluation of the fenofibrate-BGL003 conjugate as a candidate for anti-hyperlipemia drug was carried out using rats. The water-solubility of the fenofibrate-BGL003 conjugate was several thousand times greater than that of the original fenofibrate. The lipid-lowering effects of the fenofibrate-BGL003 conjugate were as strong as those of the same grams of fenofibrate. The actual active species of fenofibrate, fenofibric acid, was detected in rats' blood, but neither the fenofibrate-BGL003 conjugate nor fenofibrate was detected, probably due to enzymatic hydrolysis of the ester bond. The plasma concentration of fenofibric acid derived from the fenofibrate-BGL003 conjugate was five times higher than that derived from fenofibrate 4h after administration.

摘要

合成了三种水溶性纤维酸酯(非诺贝特、苯扎贝特和氯贝特)与对称支化甘油三酯(BGL003)的缀合物,并使用大鼠对非诺贝特-BGL003 缀合物作为抗高脂血症药物候选物进行了评估。非诺贝特-BGL003 缀合物的水溶性比原始非诺贝特高几千倍。非诺贝特-BGL003 缀合物的降血脂作用与相同克数的非诺贝特一样强。在大鼠血液中检测到了非诺贝特的实际活性物质非诺贝特酸,但未检测到非诺贝特-BGL003 缀合物或非诺贝特,这可能是由于酯键的酶水解。非诺贝特-BGL003 缀合物衍生的非诺贝特酸的血浆浓度在给药后 4 小时是源自非诺贝特的五倍。

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