- Signaling Pathways
- Metabolic Enzyme/Protease
- E1/E2/E3 Enzyme
E1/E2/E3 Enzyme
E1 activating enzyme; E2 conjugating enzyme; E3 ligating enzyme; Ubiquitin activating enzyme; Ubiquitin conjugating enzyme; Ubiquitin ligase
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E1/E2/E3 Enzyme Inhibitors
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E1/E2/E3 Enzyme Agonists
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E1/E2/E3 Enzyme Antagonist
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E1/E2/E3 Enzyme Activators
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E1/E2/E3 Enzyme Modulators
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E1/E2/E3 Enzyme Inducer
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E1/E2/E3 Enzyme Degraders
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E1/E2/E3 Enzyme Control
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E1/E2/E3 Enzyme Ligands
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Ubiquitin Enzymes Proteins
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E1/E2/E3 Enzyme Related Products (320)
Related Products (320)
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Recombinant Proteins (116)
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Antibodies (88)
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Related Compound Screening Libraries (1)
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Keap1-Nrf2-IN-4
0 ImagesCat. No.: HY-144099CAS No.: 2851480-01-6Keap1-Nrf2-IN-4 is a potent neddylation inhibitor. Keap1-Nrf2-IN-4 exhibits potent anti-proliferation activity against MGC-803 cells (IC50=2.55 µM). Keap1-Nrf2-IN-4 blocks the migration ability and induces apoptosis of gastric cancer cells. Keap1-Nrf2-IN-4 inhibits tumor growth without obvious toxicity. -
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- PRC1 ligand 1
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- EN10
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Ginkgolic Acid (Standard)
0 ImagesCat. No.: HY-N0077RCAS No.: 22910-60-7Synonyms: Ginkgolic acid (15:1) (Standard); Ginkgolic acid I (Standard); Romanicardic acid (Standard)Ginkgolic Acid (Standard) is the analytical standard of Ginkgolic Acid. This product is intended for research and analytical applications. Ginkgolic Acid is a natural compound that inhibits SUMOylation with an IC50 of 3.0 μM in in vitro assay. -
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Leucettamol A
0 ImagesCat. No.: HY-125660CAS No.: 151124-32-2Leucettamol A is an inhibitor of Ubc13 (ubiquitin E2 enzyme)-Uev1A interaction, with an IC50 of 50 μg/mL. Leucettamol A can potentially activate the expression of cancer suppressor p53 and is a precursor of anticancer agents. Leucettamol A can be isolated from a marine sponge, Leucetta aff. Microrhaphis. -
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CRBN ligand-12
0 ImagesCat. No.: HY-170058CAS No.: 2820501-20-8 -
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Hakin-1
0 ImagesCat. No.: HY-176861CAS No.: 346660-34-2Hakin-1 is a E3 Ubiquitin-Ligase Hakai inhibitor. Hakin-1 blocks Hakai-mediated global ubiquitination and specific ubiquitination of E-cadherin and inhibits epithelial-mesenchymal transition (EMT) progression. Hakan-1 inhibits tumor progression and cancer metastasis. Hakin-1 can be used for the study of carcinoma such as colorectal cancer. -
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- Cbl-b-IN-19
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p62-ZZ ligand 1
0 ImagesCat. No.: HY-168293CAS No.: 2409960-13-8p62-ZZ ligand 1 (Compound 7) is an p62-ZZ ligand. p62-ZZ ligand 1 can be used for synthesis of VinclozolinM2-2204 (HY-161741). -
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Obudanersen
0 ImagesCat. No.: HY-177651CAS No.: 2834724-31-9Synonyms: ION-582Obudanersen is an antisense oligonucleotide targeted to ubiquitin protein ligase E3A-antisense transcript (UBE3A-ATS). It is used for the study of Angelman syndrome. -
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LO-3-62
0 ImagesCat. No.: HY-175186LO-3-62 is a SMARCA2/4 degrader. LO-3-62 incorporates a truncated fumaramide linker and conjugates it to a SMARCA2/4 inhibitor. LO-3-62 binds covalently to the CUL4DCAF16 E3 ubiquitin ligase, inducing proteasome-dependent degradation of SMARCA2/4. LO-3-62 can be used in studies of monocytic leukemia. -
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Pomalidomide-β-D-glucose
0 ImagesCat. No.: HY-189288CAS No.: 2894135-13-6Pomalidomide-β-D-glucose is an orally active Molecular glue degrader of IKZF1 and CK1α. Pomalidomide-β-D-glucose forms a ternary complex with CRBN and substrate proteins, inducing ubiquitination and proteasomal degradation of IKZF1 and CK1α. Pomalidomide-β-D-glucose undergoes GLUT1-mediated cellular uptake. Pomalidomide-β-D-glucose can be used for research on multiple myeloma. -
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- PROTAC MDM2 Degrader-4
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MCULE-3064932370
0 ImagesCat. No.: HY-181772CAS No.: 315698-78-3MCULE-3064932370 is a covalent and allosteric SUMO E1 (heterodimer of Aos1 and Uba2) inhibitor with IC50 values ranging from 16.66 μM to 2.96 μM. MCULE-3064932370 inhibits SUMOylation of Uba2. MCULE-3064932370 has anti-cancer activity against breast cancer. -
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Smurf-1-IN-3
0 ImagesCat. No.: HY-157195CAS No.: 1825312-08-0Smurf-1-IN-3 is a selective Smurf-1 inhibitor with an IC50 value of 2.2 nM. Smurf-1-IN-3 can be used for the research of pulmonary arterial hypertension. -
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Cbl-b-IN-31
0 ImagesCat. No.: HY-P11479CAS No.: 3029912-63-5Cbl-b-IN-31 (Compound Pep 1) is a Cbl-b inhibitor with a Kd of 0.42 μM. Cbl-b-IN-31 is inactive in cellular assays. Cbl-b-IN-31 can be used in the research of immune-mediated diseases. -
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Rugonersen sodium scrambled negative control
0 ImagesCat. No.: HY-148130CRugonersen sodium scrambled negative control is the sequence scrambled negative control of Rugonersen sodium. -
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NAMPT activator-9
0 ImagesCat. No.: HY-182062CAS No.: 931366-46-0NAMPT activator-9 (Compound DIPM) is an allosteric, non-competitive NAMPT activator, with an EC50 of 3.366 μM against hNAMPT. NAMPT activator-9 enhances the enzymatic activity of NAMPT via an allosteric, non-competitive mechanism. NAMPT activator-9 increases intracellular NAD+ levels. NAMPT activator-9 restores myotube diameter and reduces the expression of atrophy markers Atrogin-1 and MuRF1. NAMPT activator-9 is applicable to research related to muscle atrophy. -
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DCN1-UBC12-IN-2
0 ImagesCat. No.: HY-142694CAS No.: 2374827-47-9DCN1-UBC12-IN-2 is a potent and specific DCN1-UBC12 inhibitor (IC50=9.55 nM). DCN1-UBC12-IN-2 could specifically target DCN1-UBC12 interaction and relieve Ang II-induced cardiac fibroblast activation. -
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Cbl-b-IN-6
0 ImagesCat. No.: HY-156762CAS No.: 2815221-33-9Cbl-b-IN-6 (Compound 246) is a casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl inhibitor with IC50s of 6.7 nM and 5.2 nM, respectively. -
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