PROTACs

Proteolysis-targeting chimera (PROTAC) has been developed to be a useful technology for targeted protein degradation.E3 Ligase Binder, Linker, and Target Binder are the components of PROTACs. The Target Binder is a ligand (often a small-molecule inhibitor) for the protein of interest. When the PROTACs attach to the target protein, they can recruit E3 for target protein ubiquitination, which results in proteasome-mediated destruction of the protein. Because of this, PROTACs work by destroying the target proteins rather than blocking them, which is far more effective at overcoming resistance brought on by target mutation or overexpression. In order to overcome resistance, PROTAC technology has been used on a number of targets, including AR, ER, BTK, BET, and BCR-ABL.

PROTACs related products

Structure Cat No. Product Name CAS No. Product Description
V37536 E3 ligase Ligand-Linker Conjugates 15 E3 ligase Ligand-Linker Conjugates 15comprises of a cereblon ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37537 E3 Ligase Ligand-Linker Conjugates 23 TFA E3 Ligase Ligand-Linker Conjugates 23 TFAcomprises of a cereblon ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37529 E3 ligase Ligand-Linker Conjugates 30 TFA E3 ligase Ligand-Linker Conjugates 30 TFAcomprises of a cereblon ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37559 E3 ligase Ligand-Linker Conjugates 32 hydrochloride E3 ligase Ligand-Linker Conjugates 32 hydrochloride is a lenalidomide-based ligand used in the recruitment of CRBN protein.
V37531 E3 ligase Ligand-Linker Conjugates 33 E3 ligase Ligand-Linker Conjugates 33comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37535 E3 ligase Ligand-Linker Conjugates 35 Hydrochlride E3 ligase Ligand-Linker Conjugates 35 Hydrochlridecomprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37527 E3 ligase Ligand-Linker Conjugates 37 Hydrochloride E3 ligase Ligand-Linker Conjugates 37 Hydrochloridecomprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37534 E3 ligase Ligand-Linker Conjugates 42 E3 ligase Ligand-Linker Conjugates 42comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37525 E3 ligase Ligand-Linker Conjugates 43 E3 ligase Ligand-Linker Conjugates 43comprises of an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37533 E3 ligase Ligand-Linker Conjugates 44 E3 ligase Ligand-Linker Conjugates 44comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37530 E3 ligase Ligand-Linker Conjugates 45 E3 ligase Ligand-Linker Conjugates 45comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37532 E3 ligase Ligand-Linker Conjugates 46 E3 ligase Ligand-Linker Conjugates 46comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37528 E3 ligase Ligand-Linker Conjugates 47 E3 ligase Ligand-Linker Conjugates 47comprises of an cIAP1 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V37526 E3 ligase Ligand-Linker Conjugates 48 E3 ligase Ligand-Linker Conjugates 48comprises of a MDM2 ligand for the E3 ubiquitin ligase and a PROTAC linker.
V31331 ERD-308 2320561-35-9 ERD-308 (ERD308) is a highly potent PROTAC degrader of estrogen receptor (ER) with the potential for treating ER positive breast cancer treatment (DC50: 0.17 nM (ER in MCF-7 cells)).
V67694 ERD-3111 2832865-25-3 ERD-3111 (Compound 44) is an orally bioactive PROTAC ERα degrader (DC50= 0.5 nM).
V83042 Ethyl acetate-PEG1 2093-20-1 Ethyl acetate-PEG1 is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders.
V83034 FmocNH-PEG3-CH2CH2NH2 hydrochloride 906079-91-2 FmocNH-PEG3-CH2CH2NH2 (HCl) is a PROTAC (PROteolysis TArgeting Chimera) linker, which belongs to the Polyethylene glycol (PEG) category and may be utilized to prepare PROTAC protein degraders.
V83057 galactonic acid 13382-27-9 Galactonic acid is a sugar acid, a product of the metabolic breakdown of galactose.
V69656 GBD-9 2864408-92-2 GBD-9 is a dual-mechanism degrader that efficiently degrades BTK and GSPT1 by recruiting the E3 ligase cereblon (CRBN).
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