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E1/E2/E3 Enzyme
| 货号 | 产品名 | CAS号 | 信息 |
|---|---|---|---|
| CSN23792 | VL285 | 1448188-57-5 | VL285 is a potent VHL ligand, degrading HaloTag7 fusion proteins. |
| CSN20606 | VH-298 | 2097381-85-4 | VH-298 is a highly affinity inhibitor of E3 ubiquitin ligase VHL inhibitor (Kd = 80-90 nM) which can block the interaction of VHL and HIF-α, thus initiating hypoxic response. |
| CSN17382 | TZ9 | 1002789-86-7 | TZ9 is an inhibitor of Rad6 ubiquitin conjugating enzyme (E2 enzyme) and inhibits MDA-MB-231 cell proliferation with IC50 of ~6 μM. |
| CSN22266 | E3 Ligand-Linker Conjugate 10 | 1957236-22-4 | Thalidomide-O-amido-PEG4-C2-Amine is a PROTAC block consist of Thalidomide and a linker with Amine functional group for conjugation reactions. |
| CSN22271 | E3 Ligand-Linker Conjugate 7 | 2022182-59-6 | Thalidomide-O-amido-PEG-C2-Amine is a PROTAC block consist of Thalidomide and a linker with Amine functional group for conjugation reactions. |
| CSN22272 | E3 Ligand-Linker Conjugate 6 | 2022182-57-4 | Thalidomide-O-amido-C3-Amine is a PROTAC block consist of Thalidomide linked to alkyl with Amine functional group for conjugation reactions. |
| CSN24768 | Thalidomide-linker 2 | 2245697-85-0 | Thalidomide-linker 2 is a PROTAC block consist of Thalidomide and a linker with Amine functional group for conjugation reactions. |
| CSN21424 | E3 ligase Ligand 3 | 1061605-21-7 | TC E3 5031 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component. |
| CSN17260 | SZL P1-41 | 222716-34-9 | SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes. |
| CSN25714 | SMER 3 | 67200-34-4 | SMER 3 is a selective inhibitor of yeast SCF family E3 ubiquitin ligase (SCFMet30) in vitro and in vivo. |
| CSN18199 | PRT4165 | 31083-55-3 | PRT4165, an inhibitor of bim1 and ring1A, could block PRC1 (Polycomb-repressive complex 1)-mediated H2A ubiquitylation. |
| CSN22492 | PROTAC Linker 1 | 1835705-53-7 | PROTAC Linker 1 is a linker used to link the warhead and the E3 ligase ligand. |
| CSN19741 | PK11195 | 85532-75-8 | PK11195 is a 2‑Phenylindolylglyoxylyldipeptide Murine Double Minute2 (MDM2)/Translocator Protein (TSPO)/Human Constitutive Androstane Receptor (hCAR) Inhibitor, and is potentially useful for the Treatment of Gliomas. |
| CSN17303 | NSC 697923 | 343351-67-7 | NSC 697923 is a cell-permeable and selective inhibitor of the Ub-conjugating enzyme (E2) complex Ubc13-Uev1A. |
| CSN27723 | MID-1 | 312608-54-1 | MID-1 is a MG53-IRS-1 interaction disruptor. It abolished MG53-mediated IRS-1 ubiquitination and degradation, as well as sensitized insulin signaling and increased insulin-elicited glucose uptake with an elevated level of IRS-1 in C2C12 myotubes. |
| CSN20357 | MDK7526 | 1448297-52-6 | MDK7526 is a ligand of Von Hippel–Lindau protein, that can be used for making proteolysis targeting chimeras (PROTACs). |
| CSN32744 | EMBL | 445222-91-3 | EMBL is an inhibitor of MuRF1. |
| CSN28743 | E3 ligase Ligand 9 | 87304-15-2 | E3 ligase Ligand 9 is a Bestatin-based E3 ligase ligand. |
| CSN21237 | E3 Ligase Ligand 6 | 1631137-51-3 | E3 Ligase Ligand 6 is used for conjugation reactions of PROTAC, which can hijack VHL as the E3 ubiquitin ligase component. |
| CSN21420 | E3 ligase Ligand 2 | 5054-59-1 | E3 ligase Ligand 2 is a thalidomide derivate for conjugation reactions of PROTAC, which can hijack cereblon as the E3 ubiquitin ligase component. |
| CSN33243 | tert-Butyl 4-(2-(2,6-dioxopiperidin-3-yl)-3-oxoisoindolin-5-yl)piperazine-1-carboxylate | 2229723-91-3 |
