- Signaling Pathways
- PROTAC
- Ligands for E3 Ligase
Ligands for E3 Ligase
E3 ligase-recruiting Moiety
A PROTAC (Proteolysis Targeting Chimeric Molecule) is a protein degrader comprised of a ligand for E3 ligase (E3 ligase binder), a linker and a ligand for target protein (target binder). The association between an E3 ligase and a target protein induced by a PROTAC will lead to the transfer of ubiquitin and degradation of the targeted protein.
E3 ligases catalyze the transfer of ubiquitin to targeted proteins and determine the specificity of the proteins. There are hundreds of E3 ligases in cells, but only a limited number of them are successfully used in reported PROTACs, such as VHL (von Hippel-Lindau disease tumor suppressor protein), CRBN (Cereblon), MDM2 (the mouse double minute 2 homologue) and IAP (inhibitor of apoptosis).
Ligands for E3 Ligase Isoform Specific Products
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Ligands for E3 Ligase
(106)
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von Hippel-Lindau (VHL)
(93)
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MDM2
(8)
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Cereblon
(929)
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IAP
(17)
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KLHDC2
(7)
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Fbxo3
(1)
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RNF4
(2)
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DCAF11
(3)
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DCAF1
(5)
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UHRF1
(1)
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TRIM21
(1)
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NEURL1B
(1)
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KLHL41
(1)
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RNF114
(1)
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DDB1
(1)
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FEM1B
(1)
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KEAP1
(1)
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NEDD4
(1)
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GID4
(1)
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Ligands for E3 Ligase Inhibitors
(2)
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Ligands for E3 Ligase Modulators
(2)
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Ligands for E3 Ligase Chemicals
(3)
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Ligands for E3 Ligase Degraders
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Ligands for E3 Ligase Controls
(4)
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Ligands for E3 Ligase Substrate
(1)
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Ligands for E3 Ligase Ligands
(16)
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Ligands for E3 Ligase Related Products (1206)
Related Products (1206)
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Antibodies (2)
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Related Compound Screening Libraries (1)
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Ligands for E3 Ligase Isoform Comparison
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Glutarimide
0 ImagesGlutarimide is a CRBN binder. Glutarimide exerts its function by binding to the thalidomide-binding domain of the CRBN protein. Glutarimide serves as an important structural component of many biologically active compounds. Glutarimide can be used in studies related to anemia, multiple myeloma and cycloheximide. -
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Thalidomide-NH-CH2-COOH
0 ImagesThalidomide-NH-CH2-COOH is the Thalidomide-based cereblon ligand used in the recruitment of CRBN protein. Thalidomide-NH-CH2-COOH can be connected to the ligand for protein by a linker to form PROTACs, such as THAL-SNS-032 (HY-123937). -
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- Lenalidomide-5-Br
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CCW16
0 ImagesCCW16 is a non-selective cysteine-reactive covalent ligand and an RNF4 E3 ubiquitin ligase recruiter with an IC50 of 1.8 μM against human RNF4[. CCW16 covalently modifies accessible cysteine residues on RNF4, PRDX1, PRDX2, and PRDX6, attenuating the peroxide-scavenging activity of peroxiredoxins. CCW16 induces oxidative stress through upregulation of HMOX1 and NRF2, and triggers ferroptosis via lipid peroxidation and ROS signaling pathways in an RNF4-independent manner. CCW16 serves as an RNF4-recruiting moiety; it does not induce RNF4 degradation when used alone and can be used to synthesize protein degraders, such as the PROTAC compound CCW 28-3 (HY-156774). CCW16 can be used for research on acute myeloid leukemia and hepatocellular carcinoma. -
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- Lenalidomide-Br
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- CRBN ligand-880
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VH032-cyclopropane-F
0 ImagesSynonyms: VHL ligand 3; E3 ligase Ligand 19 -
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- (S)-Thalidomide
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- CRBN ligand-397
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PLX-4545
0 ImagesCat. No.: HY-159647CAS No.: 2892065-45-9PLX-4545 is an orally active, selective molecular glue degrader targeting IKZF2. Through a molecular glue mechanism, PLX-4545 binds to CRBN, recruits IKZF2 to form a ternary complex, and promotes its ubiquitination and proteasomal degradation. This further converts inhibitory regulatory T cells (Treg) into effector-like T cells, enhances CD8+ T cell responses, and modulates the Teff:Treg balance. PLX-4545 also increases the production of the inflammatory cytokine IL-2 and reduces the suppressive activity of Treg. PLX-4545 can be used in cancer immunotherapy research, and exhibits a synergistic effect when combined with immune checkpoint inhibitors such as anti-PD1. -
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Lenalidomide (Standard)
0 ImagesSynonyms: CC-5013 (Standard)Lenalidomide (Standard) (CC-5013 (Standard)) is the analytical standard of Lenalidomide (HY-A0003). This product is intended for research and analytical applications. Lenalidomide (CC-5013) is an orally active immunomodulatory agent that binds CRBN as a molecular glue to alter substrate specificity, inducing ubiquitination and proteasome-dependent degradation of IKZF1, IKZF3 and CK1α. Lenalidomide induces apoptosis by degrading IKZF1/3, and activates p53 by degrading CK1α. Lenalidomide promotes IL-2 release and effector functions of CD8+ T/NK cells, while inhibiting TNF-α secretion and M1-type pyroptosis. Lenalidomide can be used in research related to hematological malignancies, acute liver failure and acute kidney injury. -
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- VH 101, acid
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Thalidomide (Standard)
0 ImagesThalidomide (Standard) is the analytical standard of Thalidomide. This product is intended for research and analytical applications. Thalidomide inhibits cereblon (CRBN), a part of the cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1, with a Kd of ∼250 nM, and has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties. Thalidomide can work as molecular glue to potentiate substrate. -
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- MDM2 ligand 5
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- Lenalidomide-I
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NCT02
0 ImagesNCT02 is a molecular glue degrader based on the E3 ubiquitin ligase DDB1 that targets CDK12 and its binding partner CCNK. NCT02 triggers the ubiquitination and proteasomal degradation of CCNK, thereby downregulating CDK12 protein levels and inhibiting its downstream signaling pathways. NCT02 can induce tumor cell apoptosis, arrest the cell cycle, and selectively inhibit the proliferation of colorectal cancer cells carrying TP53 defects or belonging to the consensus molecular subtype CMS4. NCT02 has the potential to inhibit tumor growth in in vitro and in vivo models. -
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Adamantan-1-ylmethanamine
0 ImagesSynonyms: 1-Aminomethyladamantane -
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- 3-(6-Amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione
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- 5,6-Difluoro-desamino lenalidomide
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(S,R,S)-AHPC-propargyl
0 ImagesSynonyms: VH032-propargyl; VHL ligand 7 -
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