6 Results for "

SJF620

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "SJF620" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-133143
CAS No.: 36839-55-1
Purity:  98.66%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

1,2-Bis(2-iodoethoxy)ethane is a PEG-based PROTAC linker. 1,2-Bis(2-iodoethoxy)ethane can be used in the synthesis of MT802 (HY-122562) and SJF620 (HY-133137). MT-802 and SJF620 are potent PROTAC BTK degraders with DC50s of 1 nM and 7.9 nM, respectively .
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Cat. No.: HY-133137
CAS No.: 2376187-16-3
Purity:  98.01%
Target:  

PROTACs Btk

Research Areas:  

Cancer

SJF620 is a PROTAC connected by ligands for Cereblon and Btk with a DC50 of 7.9 nM. SJF620 contains a Lenalidomide analog for recruiting CRBN .
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Cat. No.: HY-133144
CAS No.: 1416990-08-3
Purity:  99.48%
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

Lenalidomide-OH is an analog of cereblon (CRBN) ligand Lenalidomide for E3 ubiquitin ligase, and is used in the recruitment of CRBN protein. Lenalidomide-OH can be connected to the ligand for protein by a linker to form PROTACs, such as the PROTAC BTK degrader SJF620 (HY-133137) .
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Cat. No.: HY-133137A
CAS No.: 2821938-05-8
Target:  

PROTACs Btk

Research Areas:  

Cancer

SJF620 hydrochloride is a PROTAC connected by ligands for Cereblon and Btk with a DC50 of 7.9 nM. SJF620 contains a Lenalidomide analog for recruiting CRBN .
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Cat. No.: HY-130983
CAS No.: 2231747-18-3
Purity:  98.06%
Research Areas:  

Cancer

N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC50s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively . N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC50 of 7.9 nM .
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Cat. No.: HY-130982
CAS No.: 2738934-13-7
Research Areas:  

Cancer

Lenalidomide-PEG3-iodine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Lenalidomide based cereblon ligand and a 3-unit PEG linker. Lenalidomide-PEG3-iodine can be used in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC50 of 7.9 nM .
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