8 Results for "

PROTAC Bcl2 degrader-1

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "PROTAC Bcl2 degrader-1" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-125876
CAS No.: 2378801-85-3
Purity:  99.80%
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl2 degrader-1 (Compound C5) is a PROTAC based on Cereblon ligand, which potently and selectively induces the degradation of Bcl-2 (IC50, 4.94 μM; DC50, 3.0 μM) and Mcl-1 (IC50, 11.81 μM) by introducing the E3 ligase cereblon (CRBN)-binding ligand pomalidomide to Mcl-1/Bcl-2 dual inhibitor Nap-1 .
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1
1 Cited Publications
Cat. No.: HY-125877
CAS No.: 2163793-38-0
Purity:  98.13%
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Mcl1 degrader-1 (compound C3), a proteolysis targeting chimera (PROTAC) based on Cereblon ligand, is a potently and selectively Mcl-1 (Bcl-2 family member) inhibitor with an IC50 of 0.78 μM. PROTAC Mcl1 degrader-1 inhibits Bcl-2 with an IC50 of 0.54 μM .
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Cat. No.: HY-131188
CAS No.: 2450351-07-0
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl-xL degrader-1 is a PROTAC that comprises a Bcl-xL (Bcl-2 family member) ligand binding group, a linker and an IAP E3 ligases binding group. PROTAC Bcl-xL degrader-1 is a potent Bcl-xL degrader, and shows toxicity for human platelets and MyLa 1929 cells with IC50 values of 62 nM and 8.5 μM, respectively .
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Cat. No.: HY-178176
Research Areas:  

Cancer

PROTAC CB1R Degrader-1 is a potent and selective CB1R PROTAC degrader that exploits the ubiquitin-proteasome system (UPS) achieving a DC50 of 3.37 μM in MCF-7 cells and showing no impact on CB2R. PROTAC CB1R Degrader-1 reduces CB1R-associated downstream signaling (p-AKT, p-ERK, BCL2, and MCM5), thereby inhibiting breast cancer cell proliferation and inducing apoptosis. PROTAC CB1R Degrader-1 can be used for breast cancer research .
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Cat. No.: HY-178066
Target:  

Bcl-2 Family PROTACs

Research Areas:  

Cancer

PROTAC BCL-xL/BCL-w Degrader 1 is a selective BCL-xL/BCL-w PROTAC degrader. PROTAC BCL-xL/BCL-w Degrader 1 promotes ubiquitination and degradation of BCL-xL and BCL-w, without affecting BCL-2. PROTAC BCL-xL/BCL-w Degrader 1 can be used for the research of Hodgkin lymphoma .
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Cat. No.: HY-176421
CAS No.: 3070438-85-3
PROTAC PI3K/110β degrader-1 is a VHL-recruiting PROTAC degrader targeting PI3K/110β, with DC50 values of 0.416 μM (MCF-7) and 19.66 μM (A549), respectively. PROTAC PI3K/110β degrader-1 recruits VHL to induce proteasomal degradation of PI3K/110β. It activates endoplasmic reticulum stress (ERS)-mediated mitochondrial apoptosis via the PERK/ATF4/CHOP unfolded protein response (UPR) pathway, downregulates p-AKT and Bcl-2, upregulates Bax, cleaved-caspase-9 and cleaved-caspase-3, inhibits the expression and activity of P-gp, and exerts synergistic anti-tumor effects with Doxorubicin (Adriamycin, ADM) (HY-15142A) and Cisplatin (DDP) (HY-17394). PROTAC PI3K/110β degrader-1 can be used in research related to multidrug-resistant cancers .
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Cat. No.: HY-158551
CAS No.: 3034200-49-9
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl-2/Bcl-xL Degrader-1 is a Bcl-2/Bcl-xL PROTAC degrader with a DC50 of 11.28 nM against Bcl-xL. PROTAC Bcl-2/Bcl-xL Degrader-1 promotes ubiquitination and degradation of Bcl-2/Bcl-xL. It exhibits anticancer activity against acute lymphoblastic leukemia. PROTAC Bcl-2/Bcl-xL Degrader-1 can be used in the research of BCL-2-mediated or BCL-2-dependent diseases .
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Cat. No.: HY-158677
CAS No.: 3034202-16-6
Bcl-2/Bcl-xL ligand 1 is a Bcl-2/Bcl-xL ligand that can serve as a PROTAC target protein ligand for studies related to PROTAC synthesis, such as the synthesis of PROTAC Bcl-2/Bcl-xL Degrader-1 (HY-158551) .
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