PROTAC
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The PROTAC molecule itself contains three distinct portions: a ligand for binding to the target protein, a ligand for binding to an E3 ligase, and a linker joining these two ligands.
PROTACs (proteolysis-targeting chimaeras) are bifunctional molecules that bring a target protein into spatial proximity with an E3 ubiquitin ligase to trigger target ubiquitination and subsequent proteasomal degradation. Effective redirection of ligase poly-ubiquitination activity toward a new substrate protein requires formation of a ligase:PROTAC:target ternary complex, an intermediate species that is crucial to the cellular activity of degrader molecules. A characteristic feature of PROTACs mode of action is their sub-stoichiometric catalytic activity that alleviates the requirement for target engagement and occupancy of traditional inhibitors. New PROTAC molecules designed guided by the crystal structure show exquisite selectivity for inducing cellular depletion of Brd4 over its BET family members Brd2 and Brd3.
Products Related to PROTAC(294)
- GC91582Pomalidomide 4'-PEG5-amine (hydrochloride)CAS: 2357117-23-6Purity: >95.00%
Pomalidomide 4’-PEG5-amine is a PEGylated form of the cereblon (CRBN) inhibitor pomalidomide .
- GC91584Pomalidomide 4'-alkylC6-amine (hydrochloride)CAS: 2375194-37-7Purity: >98.00%
Pomalidomide 4'-alkylC6-amine is a building block in the synthesis of proteolysis-targeting chimeras (PROTACs) and a derivative of the cereblon inhibitor pomalidomide .
- GC91586PROTAC RAF Degrader 1CAS: 2413035-41-1Purity: >98.00%
PROTAC RAF degrader 1 is a proteolysis-targeting chimera (PROTAC) that contains the inhibitor of mutant V600E and wild-type B-RAF vemurafenib (PLX4032; ) conjugated to VHL ligand 1 .
- GF04054PROTAC CDK9 degrader-4CAS: 2411021-01-5Purity: >95.00%
PROTAC CDK9 degrader-4 is a PROTAC protein degrader that targets CDK9 (cyclin-dependent kinase 9).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC91440 | Dth | - | >95.00% | |
Dth es una quimera dirigida a la proteólisis (PROTAC) compuesta por la sonda fluorescente para ARN DFHBI y el compuesto inmunomodulador talidomida. | ||||
| GC91442 | C-02 | - | >95.00% | |
C-02 es una quimera dirigida a la proteólisis (PROTAC) compuesta por el inhibidor de hexoquinasa lonidamina unido al ligando cereblón talidomida. | ||||
| GC91582 | Pomalidomide 4'-PEG5-amine (hydrochloride) | 2357117-23-6 | >95.00% | |
Pomalidomide 4’-PEG5-amine is a PEGylated form of the cereblon (CRBN) inhibitor pomalidomide . | ||||
| GC91584 | Pomalidomide 4'-alkylC6-amine (hydrochloride) | 2375194-37-7 | >98.00% | |
Pomalidomide 4'-alkylC6-amine is a building block in the synthesis of proteolysis-targeting chimeras (PROTACs) and a derivative of the cereblon inhibitor pomalidomide . | ||||
| GC91586 | PROTAC RAF Degrader 1 | 2413035-41-1 | >98.00% | |
PROTAC RAF degrader 1 is a proteolysis-targeting chimera (PROTAC) that contains the inhibitor of mutant V600E and wild-type B-RAF vemurafenib (PLX4032; ) conjugated to VHL ligand 1 . | ||||
| GF04054 | PROTAC CDK9 degrader-4 | 2411021-01-5 | >95.00% | |
PROTAC CDK9 degrader-4 is a PROTAC protein degrader that targets CDK9 (cyclin-dependent kinase 9). | ||||
