专利号:US-2004110228-A1 优先权日:2002-04-01 标 题:Combinatorial organic synthesis of unique biologically active compounds 发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M 摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.
参考文献:10.1007/s00216-025-05834-y 摘要:Li W, Gao B, Yang T, Tang L, Song D, Li H, Sun K, Xiao P. Development and validation of an isotope dilution-liquid chromatography-tandem mass spectrometry (ID-LC-MS/MS)-based candidate reference measurement procedure for total 3,3′,5-Triiodothyronine in human serum. Anal Bioanal Chem. 2025 Mar 22;417(13):2923–33. doi: 10.1007/s00216-025-05834-y. 参考文献:10.1007/s12032-025-02745-x 摘要:Hatim MS, Al-Saffar AZ, Al-Aadhami MAWS. 5-Bromouracil-gracillin (5BrU-G) complex: an APOBEC3-activated therapeutic strategy exploiting cancer-specific enzymatic activity for selective cytotoxicity. Med Oncol. 2025 May 08;42(6):203. doi: 10.1007/s12032-025-02745-x.