- 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)
(94)
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MDM2
(8)
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Cereblon
(931)
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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
(18)
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Ligands for E3 Ligase Related Products (1209)
Related Products (1209)
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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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(R)-BMS-986470
0 ImagesCat. No.: HY-175742APurity: 99.93%(R)-BMS-986470 is the enantiomer of BMS-986470 (HY-175742). BMS-986470, a HbF-activating CRBN E3 ligase modulator (CELMoD), is an orally active dual molecular glue degrader targeting ZBTB7A and WIZ. -
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Lenalidomide-d5
0 ImagesSynonyms: CC-5013-d5Lenalidomide-d5 (CC-5013-d5) is the d5-labeled Lenalidomide (HY-A0003). 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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- E3 ligase Ligand 8
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Thalidomide-5-methyl
0 ImagesThalidomide-5-methyl is the Thalidomide (HY-14658)-based cereblon (CRBN) ligand used in the recruitment of CRBN protein. Thalidomide-5-methyl can be used to synthesize PROTAC. -
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- CRBN ligand-9
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VH032 thiol
0 ImagesCat. No.: HY-111823CAS No.: 2098836-54-3Synonyms: VHL ligand 6VH032 thiol (VHL ligand 6) is a VHL ligand, which binds to pan-BET inhibitor JQ1 via a linker to form PROTAC. -
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- DCAF1 ligand 2
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PROTAC PLK1 Degrader-2
0 ImagesCat. No.: HY-180989Purity: 99.48%PROTAC PLK1 Degrader-2 is a peptide-based N-end rule PLK1 mini-PROTAC. PROTAC PLK1 Degrader-2 utilizes Arg12 as dual-function cell-permeable N-degron to recruit UBR1/UBR2 E3 ligases, mediates PLK1 ubiquitination and proteasome-dependent degradation. PROTAC PLK1 Degrader-2 suppresses cervical cancer cell proliferation, induces G2/M cell cycle arrest and tumor cell apoptosis, and exerts potent in vivo anti-tumor efficacy in mice and can be applied to research on PLK1-driven cervical carcinoma (PLK1 ligand: POI ligand-3 (HY-180990); E3 ligase ligand: Arg12 (HY-P11631); PROTAC linker: 6-Aminocaproic acid (HY-B0236)). -
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SJF-0661
0 ImagesCat. No.: HY-157512CAS No.: 2413035-43-3SJF-0661 is a variant of the von Hippel-Lindau (VHL) protein ligand with no targeted degradation ability and can be used as a control reagent for the VHL ubiquitin ligase ligand. SJF-0661 is a variant obtained by inverting the stereocenter of the key hydroxyproline group in the VHL ligand. -
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VL285 Phenol
0 ImagesCat. No.: HY-151227CAS No.: 1448188-69-9VL285 Phenol is a phenol-based VL285 analog. VL285 is an E3 ubiquitin ligase VHL ligand and can be used in the synthesis of HaloPROTAC3, degrading HaloTag7 fusion protein (IC50=0.34 μM). -
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- CRBN ligand-187
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Pomalidomide-15N,13C5
0 ImagesCat. No.: HY-10984S3Synonyms: CC-4047-15N,13C5Pomalidomide-15N,13C5 is 15N and 13C labeled Pomalidomide (HY-10984). Pomalidomide, the third-generation immunomodulatory agent, acts as molecular glue. Pomalidomide interacts with the E3 ligase cereblon and induces degradation of essential Ikaros transcription factors. -
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CRBN ligand-789
0 ImagesCat. No.: HY-W873806CAS No.: 2304754-82-1 -
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- (R)-Desamino lenalidomide-5-Br
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CRBN ligand-206
0 ImagesCat. No.: HY-W998252CAS No.: 1486115-10-9 -
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5-Fluoro-lenalidomide
0 ImagesCat. No.: HY-W875713CAS No.: 1918158-58-3 -
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Pomalidomide-COCH2Cl
0 ImagesPomalidomide-COCH2Cl is a derivative of Pomalidomide with an chloroacetamide group on the benzyl ring. -
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- Thalidomide-iodo
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Desamino lenalidomide-6-propyne
0 ImagesCat. No.: HY-W589407CAS No.: 2412439-22-4 -
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- Thalidomide-1-Me-5-NH2
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