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Cat. No. Product Name Target Signaling Pathways
T18681 SJFα

Others Others
SJFα is a 13-atom linker PROTAC. SJFα degrades p38α with a DC50 of 7.16 nM, but is far less effective at degrading p38δ (DC50=299 nM) and does not degrade the other p38 isoforms (β and γ) at concentrations up to 2.5 μM[1].
T36244 SJF 1521

Selective EGFR Degrader. Comprises the EGFR inhibitor lapatinib (Cat. No. 6811) joined by a linker to a von Hippel-Lindau (VHL) recruiting ligand. Exhibits selectivity for EGFR, including mutant forms, over HER2. Induces degradation of EGFR in OVCAR8 cells.
T36245 SJF 1528

Potent EGFR Degrader (DC50 values are 39.2 nM for wild-type EGFR in OVCAR8 cells and 736 nM for Exon20Ins mutated EGFR in HeLa cells). Also degrades HER2. Comprises the EGFR inhibitor lapatinib (Cat. No. 6811) joined by a linker to a von Hippel-Lindau (VHL) recruiting ligand. Inhibits proliferation of HER2-driven breast cancer cell lines (IC50 = 102 nM for SKBr3 cells).
T41168 SJF 0661

SJF 0661 is the negative control for SJF 0628. Binds BRAF without inducing degradation.
T36246 SJF 8240

c-MET degrader. Comprises MET inhibitor foretinib (GSK 1363089; Cat. No. 6056) joined by a linker to a von Hippel-Lindau (VHL) recruiting ligand. Degrades c-MET within 6 hours in vitro. Inhibits agonist-driven AKT phosphorylation and GTL16 cell proliferation (IC50 = 66.7 nM). Also degrades exon-14-deleted c-MET in Hs746T cells.
T74002 SJF620 hydrochloride

PROTACs PROTAC
SJF620 hydrochloride,作为一种连接Cereblon配体和Btk配体的PROTAC,具备DC50值为7.9 nM。该化合物含Lenalidomide类似物,能有效募集CRBN。

化合物

SJFα
Cat.No: T18681
Synonym:
Target: Others
SJF 1521
Cat.No: T36244
Synonym:
Target:
SJF 1528
Cat.No: T36245
Synonym:
Target:
SJF 0661
Cat.No: T41168
Synonym:
Target:
SJF 8240
Cat.No: T36246
Synonym:
Target:
SJF620 hydrochloride
Cat.No: T74002
Synonym:
Target: PROTACs
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