9 Results for "

Rpn13

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "Rpn13" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-100739
CAS No.: 1617495-03-0
Purity:  99.04%
Target:  

Proteasome

Research Areas:  

Cancer

RA190, a bis-benzylidine piperidon, inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.
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Cat. No.: HY-136563
CAS No.: 2649154-57-2
Purity:  99.31%
Research Areas:  

Cancer

RA375 is a RPN13 (26S proteasome regulatory subunit) inhibitor. RA375 activates UPR signaling, ROS production and apoptosis. RA375 exhibits ten-fold greater activity against cancer lines than RA190, reflecting its nitro ring substituents and the addition of a chloroacetamide warhead .
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Cat. No.: HY-172822
Target:  

ByeTAC Btk

Research Areas:  

Cancer

TLT8 is a ByeTAC protein degrader targeting BTK. TLT8 non-covalently binds to Rpn-13 and BTK, thereby inducing BTK degradation. TLT8 can be used in chronic lymphocytic leukemia research. (Rpn-13 ligand: HY-159808; BTK ligand: HY-Z3101; linker: HY-172823) .
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Cat. No.: HY-159808
CAS No.: 875165-39-2
Target:  

Proteasome

Research Areas:  

Cancer

TCL1 is a selective non-covalent inhibitor targeting the Pru domain of the Rpn-13 subunit in the 19S regulatory particle (19S RP) of the proteasome with an IC50 value of approximately 26 μM. TCL1 interferes with the recognition and transport of ubiquitinated proteins by Rpn-13, inhibits the degradation of proteins by the proteasome, and thus affects the balance of intracellular protein metabolism. TCL1 is promising for research of hematological malignancies .
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Cat. No.: HY-176071
Research Areas:  

Cancer

TEC 4 is a ByeTAC (Bypassing E-Ligase-Targeting Chimera) BRD4 degrader, with 33% BRD4 remaining at 500 nM in Ramos B-cells. TEC 4 shows toxicity for Ramos B-cells, with an IC50 of 30.5 nM. ByeTACs directly recruits a protein to the proteasome via interactions with Rpn-13 for degradation. Pink: BRD4 lignad (HY-78695); Blue: Rpn-13 ligand (HY-159808); Black: linker (HY-W008352) .
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Cat. No.: HY-187439
Target:  

PROTACs ByeTAC Proteasome

Research Areas:  

Cancer

Truly-4 is a bifunctional Rpn13 PROTAC and CRBN ByeTAC degrader. Degradation of Rpn13 relies on CRBN-mediated E3 ubiquitin ligase activity, while degradation of CRBN itself proceeds via a ByeTAC mechanism of action. Truly-4 induces selective cytotoxicity in hematological cancer cells and solid cancer cells, but not in healthy cells, despite comparable levels of Rpn13 depletion in both cell types. Truly-4 can be used in studies related to B-cell lymphoma and triple-negative breast cancer .
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Cat. No.: HY-187440
CAS No.: 3119089-68-5
TCL1-PEG4-C2-NH2 (Compound 3) is a conjugate of a Rpn13 ligand and a linker, which can be used to synthesize PROTACs such as Truly-4 (HY-187439) .
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Cat. No.: HY-100739R
CAS No.: 1617495-03-0
Research Areas:  

Cancer

RA190 (Standard) is the analytical standard of RA190 (HY-100739). This product is intended for research and analytical applications. RA190, a bis-benzylidine piperidon, inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.
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Cat. No.: HY-181495
CAS No.: 2375455-53-9
RAJQ14 is a BRD4 PROTAC-like CAP-TAC (Proteasome Cap Targeting Chimeras) degrader. RAJQ14 binds to 19S proteasome cap subunits RPN1, RPN10, RPN13, and USP14 to recruit target proteins to the proteasome for ubiquitination-independent, proteasome-dependent degradation. RAJQ14 can be used for the research of cancer (Pink: BRD4 Ligand (HY-181496); Blue: Proteasome Ligand (HY-128978); Black: Linker).
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