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Proteasome Related Products (291)
Related Products (291)
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Antibodies (22)
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Phepropeptin A
0 ImagesCat. No.: HY-N14927CAS No.: 396729-23-0Phepropeptin A, a microbial secondary metabolite, is a proteasome inhibitor with an IC50 of 21 μg/mL. -
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Phepropeptin C
0 ImagesCat. No.: HY-N14929CAS No.: 396729-25-2Phepropeptin C, a microbial secondary metabolite, is a proteasome inhibitor with an IC50 of 12.5 μg/mL. -
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BI-1942
0 ImagesCat. No.: HY-168904CAS No.: 1236524-95-0BI-1942, a chemical probe, is a chymase inhibitor and has an IC50 of 0.4 nM for human chymase. BI-1942 can be used in the research of ophthalmic diseases. -
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KZR-504 (Standard)
0 ImagesCat. No.: HY-101786RCAS No.: 1629052-78-3KZR-504 (Standard) is the analytical standard of KZR-504 (HY-101786). This product is intended for research and analytical applications. KZR-504 is a highly selective inhibitor of immunoproteasome low molecular mass polypeptide 2 (LMP2), with IC50s of 51 nM, 4.274 μM for LMP2 and LMP7, respectively. KZR-504 is of interest for the treatment of autoimmune disease. -
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SARS-CoV-2 3CLpro-IN-34
0 ImagesCat. No.: HY-179612SARS-CoV-2 3CLpro-IN-34 (Compound 55) is a highly efficient non-covalent inhibitor of the SARS-CoV-2 3CLpro protease (b. SARS-CoV-2 3CLpro protease) with an IC50 of 1.9 μM. SARS-CoV-2 3CLpro-IN-34 can inhibit the 3CLpro protein of SARS-CoV-1, with its IC50 being 3.2 μM, and it shows high selectivity towards host cysteine proteases (such as cathepsins L/K and calpain). SARS-CoV-2 3CLpro-IN-34 exhibits antiviral activity in cells infected with SARS-CoV-2, with its EC50 being 25 μM, and it is not affected by P-gp inhibitors and shows no significant cytotoxicity. SARS-CoV-2 3CLpro-IN-34 can be used for research on SARS-CoV-2 infection. -
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RA190 (Standard)
0 ImagesCat. No.: HY-100739RCAS No.: 1617495-03-0RA190 (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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PD150606 (Standard)
0 ImagesCat. No.: HY-100529RCAS No.: 179528-45-1PD150606 (Standard) is the analytical standard of PD150606 (HY-100529). This product is intended for research and analytical applications. PD 150606 is a selective, cell-permeable non-peptide calpain inhibitor with Ki values of 0.21 μM and 0.37 μM for μ- and m-calpains respectively, which is neuroprotective. -
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10-Undecenoic acid (copper)
0 ImagesCat. No.: HY-B0914BCAS No.: 35322-29-3Synonyms: Undecylenic acid (copper)10-Undecenoic acid copper (Undecylenic acid copper) is an antifungal agent. 10-Undecenoic acid copper inhibits Aβ oligomerization, scavenges ROS and inhibits μ-calpain activity. 10-Undecenoic acid copper has neuroprotective effects. 10-Undecenoic acid copper has anticancer effects on a variety of tumors. 10-Undecenoic acid copper inhibits C. albicans biofilm formation and MRSA infection. 10-Undecenoic acid copper inhibits quorum sensing signals of Bacillus subtilis and Pseudomonas aeruginosa. -
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RID-F
0 ImagesCat. No.: HY-113824CAS No.: 1020853-03-5Synonyms: Ridaifen-FRID-F (Ridaifen-F), a Tamoxifen (HY-13757A) derivative, is a nonpeptidic proteasome inhibitor. RID-F inhibits human 20S proteasome activity, with IC50s of 0.64, 0.34, and 0.43 μM for CT-L, T-L, and PGPH, respectively. -
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Chymase-IN-2
0 ImagesCat. No.: HY-U00282CAS No.: 936366-22-2Chymase-IN-2 is a chymase modulator which is useful in the treatment of inflammatory and serine protease mediated disorders. -
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Neurodegenerative Disorder-Targeting Compound 1
0 ImagesCat. No.: HY-U00362CAS No.: 1254698-39-9Neurodegenerative Disorder-Targeting Compound 1 is a calpain inhibitor extracted from patent WO2010128102A1, compound example 63. -
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