Piperazine-Fused Cyclic Disulfides Unlock High-Performance Bioreductive Probes of Thioredoxins and Bifunctional Reagents for Thiol Redox Biology
作者:Lukas Zeisel、Jan G. Felber、Karoline C. Scholzen、Carina Schmitt、Alexander J. Wiegand、Leonid Komissarov、Elias S.J. Arnér、Oliver Thorn-Seshold
DOI:10.1021/jacs.3c11153
日期:2024.2.28
six-membered-cyclic disulfides as redox substrates that unlock best-in-class bioreduction probes for live cell biology, since their self-immolation after reduction is unprecedentedly rapid. We develop scalable, diastereomerically pure, six-step syntheses that access four key cis- and trans-piperazine-fused cyclic dichalcogenides without chromatography. Fluorogenic redox probes using the disulfide piperazines
Alkylating Agents Related to 2,2′-Biaziridine. II.<sup>1</sup> N,N′-Dicarbethoxy-2,2′-biaziridine
作者:Peter W. Feit、Ole Tvaermose. Nielsen
DOI:10.1021/jm00317a039
日期:1967.9
DISULFIDE-BASED PRODRUG COMPOUNDS
申请人:Ludwig-Maximilians-Universität München
公开号:EP4062942A1
公开(公告)日:2022-09-28
The present application relates to a compound having the formula (I)
A-L-B (I)
wherein
A is represented by
L is a bond or a self-immolative spacer;
B is represented by
The compound is capable of releasing molecular cargo in the presence of a reductase and is thus suitable for treating, ameliorating, preventing or diagnosing a disorder selected from a neoplastic disorder; atherosclerosis; an autoimmune disorder; an inflammatory disease; a chronic inflammatory autoimmune disease; ischaemia; and reperfusion injury.