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PEG-based PROTAC linker that can be used in the synthesis of PROTACs
InChiKey: XUARBCHSPWMKRC-UHFFFAOYSA-N
Bollmann A
LY3000328 is a Cathepsin S inhibitor with excellent in vitro potency and selectivity against other cysteine proteases
Lithocholic acid analogues
(R)-FT671 e-1 3-dione PEG-based PROTAC linker that can(R) FT671 is the R isomer of FT671. FT671 is a potent, non covalent and selective USP7 inhibitor with an IC50 of 52 nM and binds to the USP7 catalytic domain with a Kd of 65 nM. Product information CAS Number: 1959551 27 9 Molecular Weight: 533. 48 Formula: C24H23F4N7O3 Chemical Name: 5 ({1 [(3R) 4,4 difluoro 3 (3 fluoro 1H pyrazol 1 yl)butanoyl] 4 hydroxypiperidin 4 yl}methyl) 1 (4 fluorophenyl) 1H,4H,5H pyrazolo[3,4 d]pyrimidin 4 one Smiles:
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