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Proteasome Inhibitors
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Proteasome Activators
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Proteasome Substrates
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Proteasome Ligands
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Proteasome Related Products (293)
Related Products (293)
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Antibodies (22)
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Baceridin
0 ImagesCat. No.: HY-P4910CAS No.: 1622872-91-6Baceridin is a proteasome inhibitor and a cyclic hexapeptide. Baceridin can be isolated from the culture medium of Epiphytic Bacillus. Baceridin can inhibit cell cycle progression and induce tumor cell apoptosis through a p53-independent pathway. Baceridin can be used in cancer research. -
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Suc-Ala-Ala-Pro-Phe-SBzl
0 ImagesCat. No.: HY-P4580CAS No.: 80651-95-2Suc-Ala-Ala-Pro-Phe-SBzl can be used as the substrate of rat intestinal mast cell protease (RMCP I), rat skeletal muscle mast cell protease (RMCP II) and Chymotrypsin (HY-108910). Suc-Ala-Ala-Pro-Phe-SBzl can be hydrolyzed by glycine (R208G). -
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Suc-Leu-Leu-Val-Tyr-AMC (solution)
0 ImagesCat. No.: HY-DY1060CAS No.: 94367-21-2Suc-Leu-Leu-Val-Tyr-AMC (solution) is a membrane-permeable calpain-specific fluorogenic substrate (Ex/Em = 390/480 nm) .
Solvent and concentration: DMSO: 20 mM -
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Sadopeptins A
0 ImagesCat. No.: HY-N11620Sadopeptins A is a nature product that could be isolated from Streptomyces sp. Sadopeptins A is a potent proteasome inhibitor. -
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Proteasome-activating peptide 1
0 ImagesCat. No.: HY-P3414CAS No.: 1565763-62-3Proteasome-activating peptide 1 is a peptide, which increases the chymotrypsin-like proteasomal catalytic activity and, consequently, proteolytic rates both in vitro and in culture. Proteasome-activating peptide 1 prevents protein aggregation in a cellular model of amyotrophic lateral sclerosis. -
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RC-106
0 ImagesCat. No.: HY-158197CAS No.: 1346216-50-9RC-106 is a proteasome inhibitor (IC50: 35 μM) and Sigma receptor modulator with anticancer activity. RC-106 has antiproliferative activity against cancer cells including glioblastoma (GB) and multiple myeloma (MM). -
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LMP7-IN-1
0 ImagesCat. No.: HY-142920CAS No.: 2671040-07-4LMP7-IN-1, a Boronic acid derivative, is a potent and selective immunoproteasome subunit LMP7 (β5i) inhibitor with an IC50 of 1.83 nM (WO2021143923A1; compound 20). -
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Z-Leu-Tyr-Chloromethylketone
0 ImagesCat. No.: HY-P4293CAS No.: 56979-35-2Z-Leu-Tyr-Chloromethylketone is a calpain inhibitor. -
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RAPRMT5
0 ImagesCat. No.: HY-181521CAS No.: 2721998-42-9 -
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Bortezomib (GMP)
0 ImagesCat. No.: HY-10227GSynonyms: PS-341 (GMP); LDP-341 (GMP); NSC 681239 (GMP)Bortezomib (GMP) (PS-341 (GMP)) is Bortezomib (HY-10227) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. Bortezomib (PS-341) is a reversible and selective proteasome inhibitor, and potently inhibits 20S proteasome (Ki=0.6 nM) by targeting a threonine residue. Bortezomib disrupts the cell cycle, induces apoptosis, and inhibits NF-κB. Bortezomib is the first proteasome inhibitor anticancer agent. Bortezomib can be used for the study of multiple myeloma (MM). Bortezomib effectively inhibits TREM2 expression in tumor-associated macrophages (TAMs). -
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9-cis-UAB30
0 ImagesCat. No.: HY-129108CAS No.: 205252-57-9Synonyms: (9Z)-UAB-309-cis-UAB30 is a rexinoid agonist. 9-cis-UAB30 significantly decreases the proliferation, viability, and motility of both patient-derived xenografts (PDXs). 9-cis-UAB30 induced cell-cycle arrest as demonstrated by the significant increase in the percentage of cells in G1 and a decrease in the percentage of cells in S phase by downregulating SKP2 and/or 20S proteasome activity, which leads to increased p27kip1 protein stability. 9-cis-UAB30 downregulates the abundance of stem cell marker mRNAs (Oct4, Nanog, Sox2, nestin) and upregulates the abundance of differentiation marker mRNAs (β3-tubulin, NSE, HOXC9, GAP43). 9-cis-UAB30 has no adverse effects on the central nervous system and cardiovascular system at the tested dose. 9-cis-UAB30 can be used for the study of neuroblastoma, cutaneous T-cell lymphomas, and breast cancer. -
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Proteasome-IN-4
0 ImagesCat. No.: HY-144369CAS No.: 3033388-83-6Proteasome-IN-4 is an excellent and non-covalent proteasome inhibitor (IC50=8.39 nM). Proteasome-IN-4 has potent antiproliferative activities against RPMI-8226, MM-1S and MV-4-11 cell lines. Proteasome-IN-4 can be used for cancer research. -
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BC-05
0 ImagesCat. No.: HY-149514CAS No.: 2260717-73-3BC-05 is an orally active and potent inhibitor of CD13 and proteasome. BC-05 has an IC50 value of 0.13 μM for human CD13 and an IC50 value of 1.39 μM for the 20S proteasome. BC-05 can be used in multiple myeloma research. -
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PSI TFA
0 ImagesCat. No.: HY-P1258ASynonyms: Proteasome Inhibitor 1 TFA; Z-Ile-Glu(OtBu)-Ala-Leu-CHO TFAPSI (TFA) is a potent proteasome inhibitor. PSI (TFA) inhibits the proliferation of primary effusion lymphoma (PEL) cells. PSI (TFA) can be used for the research of Kaposi’s sarcoma-associated herpesvirus (KSHV) infection and KSHV-associated lymphomas. -
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Leptosphaerodione
0 ImagesCat. No.: HY-N10332CAS No.: 138039-33-5Leptosphaerodione, isolated from Remotididymella sp. Fungus, is a potent ubiquitin-proteasome system (UPS) inhibitor. Leptosphaerodione exhibits cytotoxicity in HeLa cells with IC50 value of 3.2 μM. Anti-tumor agent. -
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- Crocapeptin C
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Proteasome-IN-1
0 ImagesCat. No.: HY-100172CAS No.: 374080-21-4Proteasome-IN-1 is a proteasome inhibitor extracted from patent WO 2013142376 A1. -
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Tyropeptin A-4
0 ImagesCat. No.: HY-126874CAS No.: 688737-89-5Synonyms: TP-101Tyropeptin A-4 (TP-101) is a potent proteasome inhibitor with the ability to inhibit mammalian 20S proteasome activity. Tyropeptin A-4 exerts its inhibitory effect by binding to the site responsible for trypsin-like activity. Tyropeptin A-4 derivative TP-104 has a 20-fold increase in inhibitory activity over Tyropeptin A. TP-110 specifically inhibits trypsin-like activity without affecting PGPH and trypsin-like activity. -
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RAJQ14
0 ImagesCat. No.: HY-181495CAS No.: 2375455-53-9RAJQ14 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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Ac-RLR-AMC TFA
0 ImagesCat. No.: HY-135070BSynonyms: Ac-Arg-Leu-Arg-AMC TFAAc-RLR-AMC (Ac-Arg-Leu-Arg-AMC) TFA is a fluorogenic substrate for the 26S proteasome (Ex/Em: 380/440-460 nm). AMC is released upon cleavage, and its fluorescence can be used to quantify the trypsin-like activity of 26S proteasomes. -
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