Suzuki Toshinori, Kitabatake Akihiko, Koide Yuki
School of Pharmacy, Shujitsu University.
Chem Pharm Bull (Tokyo). 2016;64(8):1235-8. doi: 10.1248/cpb.c16-00138.
When thymidine was treated with hypobromous acid (HOBr) in 100 mM phosphate buffer at pH 7.2, two major product peaks appeared in the HPLC chromatogram. The products in each peak were identified by NMR and MS as two isomers of 5-hydroxy-5,6-dihydrothymidine-6-phosphate (a novel compound) and two isomers of 5,6-dihydroxy-5,6-dihydrothymidine (thymidine glycol) with comparable yields. 5-Hydroxy-5,6-dihydrothymidine-6-phosphate was relatively stable, and decomposed with a half-life of 32 h at pH 7.2 and 37°C generating thymidine glycol. The results suggest that 5-hydroxy-5,6-dihydrothymidine-6-phosphate in addition to thymidine glycol may have importance for mutagenesis by the reaction of HOBr with thymine residues in nucleotides and DNA.
当胸腺嘧啶核苷在pH 7.2的100 mM磷酸盐缓冲液中用次溴酸(HOBr)处理时,高效液相色谱图中出现了两个主要产物峰。通过核磁共振(NMR)和质谱(MS)鉴定每个峰中的产物为5-羟基-5,6-二氢胸腺嘧啶核苷-6-磷酸(一种新型化合物)的两种异构体以及5,6-二羟基-5,6-二氢胸腺嘧啶核苷(胸腺嘧啶二醇)的两种异构体,产率相当。5-羟基-5,6-二氢胸腺嘧啶核苷-6-磷酸相对稳定,在pH 7.2和37°C下以32小时的半衰期分解生成胸腺嘧啶二醇。结果表明,除了胸腺嘧啶二醇外,5-羟基-5,6-二氢胸腺嘧啶核苷-6-磷酸可能在HOBr与核苷酸和DNA中的胸腺嘧啶残基反应导致的诱变中具有重要作用。