- Signaling Pathways
- PROTAC
- Ligands for Target Protein for PROTAC
Ligands for Target Protein for PROTAC
Target Protein-binding Moiety
The PROTAC molecule consists of a target protein ligand and an E3 ubiquitin ligase ligand, with a linker binds them together. The ligand for target protein will lead to attachment of a PROTAC to the proteins of interest for ubiquitin and subsequent degradation.
Target proteins are usually proteins whose overexpression or accumulation may play important roles in the progress of diseases. Numbers of PROTACs have been developed to degrade kinases (such as MEK, KRAS, CDK and Bcr/Abl), transcription factors (such as p53, STAT, RAR, ER and AR), epigenetic tools (such as HDAC and BET bromodomain) and E3 ligase themselves (such as MDM2).
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Ligands for Target Protein for PROTAC Inhibitors
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Ligands for Target Protein for PROTAC Chemicals
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Ligands for Target Protein for PROTAC Degrader
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Ligands for Target Protein for PROTAC Controls
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Ligands for Target Protein for PROTAC Ligands
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Ligands for Target Protein for PROTAC Related Products (688)
Related Products (688)
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Related Compound Screening Libraries (1)
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Temozolomide-amino hydrochloride
0 ImagesCat. No.: HY-169439CAS No.: 449187-98-8Temozolomide-amino hydrochloride (compound 8) is an activity control for the target protein ligand of Naph-Se-TMZ (HY-169433). -
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- HDAC6 ligand-3
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AR antagonist 14
0 ImagesCat. No.: HY-172624CAS No.: 2757424-54-5 -
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- ERK5 ligand-2
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Naproxen Gilteritinib
0 ImagesCat. No.: HY-169374CAS No.: 1373410-40-2Naproxen Gilteritinib is the active reference substance of Gilteritinib (HY-12432). Gilteritinib is the target protein ligand of PROTAC degrader LWY713 (HY-157213). -
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KAL-21404358
0 ImagesCat. No.: HY-164326CAS No.: 1065573-84-3KAL-21404358 is a ligand for target protein for pROTAC. -
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- UNC0642-C3-COOH
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- POI-4
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SPRT
0 ImagesCat. No.: HY-161394SPRT is a short peptide of RB transcriptional corepressor 1 (RB), serving as a fragment of RB-CO-PEG5-C2-CO-VH032 (HY-161393) for the synthesis of PROTAC. -
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- BI 7271
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- SMARCA2 ligand-10
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Axl ligand-1
0 ImagesCat. No.: HY-184184CAS No.: 3033401-32-7Axl ligand-1 is a highly selective ligand for AXL kinase, exhibiting higher selectivity for AXL over 72 human kinases. Axl ligand-1 serves as a Ligand for Target Protein for PROTAC, which is applied to develop PROTAC degraders with anti-tumor activity, such as PROTAC Axl Degrader 1 (HY-144624). Axl ligand-1 is applicable to breast cancer-related research. -
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CBP/EP300 ligand-1
0 ImagesCat. No.: HY-175898CAS No.: 3054145-02-4CBP/EP300 ligand-1 is a ligands for target protein for PROTAC. CBP/EP300 ligand-1 can be used to synthesize PROTAC Pomalidomide-NH-PEG6-amide-C2-CPI-1612 (HY-161250). -
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OBHSA
0 ImagesCat. No.: HY-167701CAS No.: 1404508-27-5OBHSA is a selective estrogen receptor (ERα) degrader. OBHSA blocks the cell cycle by degrading cyclin D1, thereby overcoming Tamoxifen (HY-13757A) resistance. OBHSA also triggers excessive activation of the unfolded protein response (UPR) by inducing an increase in intracellular reactive oxygen species, ultimately leading to cell apoptosis. In addition, OBHSA can also be used as an ERα ligand to synthesize PROTAC degraders. -
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- BCL6 ligand-9
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BET-IN-30
0 ImagesCat. No.: HY-181735BET-IN-30 (Compound 11d) is a BTE family protein inhibitor, which can act as a BRD2/BRD3/BRD4 target protein ligand and be used for the synthesis of PROTACs, such as PROTAC BET Degrader-15 (HY-181729). BET-IN-30 exhibits potent anti-proliferative activity against acute myeloid leukemia (AML) cells such as MV4-11. BET-IN-30 can be used for the study of AML. -
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- KRAS ligand 1
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ALK protein ligand-1
0 ImagesCat. No.: HY-169482CAS No.: 2764870-80-4 -
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- IDO1 ligand-2
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- RIPK1-IN-37
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