Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University.
Chem Pharm Bull (Tokyo). 2021;69(2):155-177. doi: 10.1248/cpb.c20-00820.
The biologically active, naturally occurring 1,2,3,4-tetrahydroisoquinoline-quinone (THIQ) family members isolated from Actinomycetes and marine organisms have been studied thoroughly over the past five decades. Among them, marine natural products along with their reduced compounds, such as renieramycins and ecteinascidins, have attracted interest due to their fantastic structures and meager availability in nature as well as their potent antitumor profiles. As part of our search for new anticancer metabolites through the isolation and characterization of anticancer THIQ compounds from Thai marine animals, we have developed a fascinating THIQ natural product chemistry and medicinal chemistry based on knowledge of the chemistry of saframycin antibiotics as well as their isolation, characterization, transformation, partial synthesis, and total synthesis. This review mainly presents our contributions during 1999-2019 to the field of research on biologically active renieramycin along with ecteinascidin marine natural products.
在过去的五十年中,人们对从放线菌和海洋生物中分离出来的具有生物活性的天然 1,2,3,4-四氢异喹啉-醌(THIQ)家族成员进行了深入研究。其中,海洋天然产物及其还原化合物,如雷尼霉素和海鞘素,因其奇特的结构、在自然界中的稀缺性以及强大的抗肿瘤特性而引起了人们的兴趣。作为通过从泰国海洋动物中分离和鉴定抗癌 THIQ 化合物来寻找新抗癌代谢物的一部分,我们在 saframycin 抗生素化学及其分离、鉴定、转化、部分合成和全合成知识的基础上,发展了一种引人入胜的 THIQ 天然产物化学和药物化学。这篇综述主要介绍了我们在 1999-2019 年期间在生物活性雷尼霉素和海鞘素海洋天然产物研究领域的贡献。