5 Results for "

proteome-wide selectivity

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "proteome-wide selectivity" in MCE Product Catalog:

Cat. No.: HY-D2910
CAS No.: 2089058-15-9
Ox4 is a selective covalent modifier targeting Methionine residues. Ox4 is promising for research of protein functionalization, antibody-drug conjugate (ADC) synthesis, and proteome-wide identification of reactive methionine sites .
loading...
    loading...
Cat. No.: HY-132975
CAS No.: 2231405-64-2
Target:  

Bacterial

Research Areas:  

Others

PrDiAzK is a bifunctional amino acid. PrDiAzK can be site-selectively incorporated into proteins in both bacterial and mammalian cell culture. PrDiAzK can be used for proteome-wide incorporation via stochastic orthogonal recoding of translation (SORT) . PrDiAzK is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
loading...
    loading...
Cat. No.: HY-179512
CAS No.: 2414478-45-6
Target:  

PROTACs FAK

Research Areas:  

Cancer

BSJ-04-146 is a highly efficient and selective PROTAC targeting focal adhesion kinase (FAK) inhibitor(IC50 = 26 nM). BSJ-04-146 achieves rapid and potent FAK degradation with high proteome-wide specificity in cancer cells and induces durable degradation in mice. BSJ-04-146 binds FAK and requires the ubiquitin-proteasome machinery to achieve FAK degradation. BSJ-04-146 can be used for the study of pancreatic cancer and triple-negative breast cancer .
loading...
    loading...
Cat. No.: HY-182766
CAS No.: 3102636-19-8
Research Areas:  

Cancer

AMX-883 a selective and orally active BRD9 molecular glue degrader that drives differentiation in acute myeloid leukaemia. AMX-883 shows selectivity over all other bromodomain containing proteins and proteome wide. AMX-883 does not employ the commonly used E3 ligases (cereblon, VHL) but instead drives degradation via DCAF16 as a targeted glue. AMX-883 can be used for the study of acute myeloid leukaemia (AML) .
loading...
    loading...
Cat. No.: HY-187694
CAS No.: 2400958-08-7
Target:  

PIN1 Ras

Research Areas:  

Cancer

BJP-06-005-3 is a selective Pin1 inhibitor with a Ki value of 48 nM. BJP-06-005-3 induces the degradation of mutant KRAS. BJP-06-005-3 inhibits pancreatic ductal adenocarcinoma via the Pin1-mediated pathway. BJP-06-005-3 is used in studies related to KRAS-mutant pancreatic ductal adenocarcinoma .
loading...
    loading...