| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V104289 | (S)-Deoxy-thalidomide-2,7-diazaspiro[3.5]nonane-C-Pip | (S)-Deoxy-thalidomide-2,7-diazaspiro[3.5]nonane-C-Pip is an E3 ubiquitin ligase ligand + linker conjugate used in the synthesis of PROTAC FHD-609. | |
|
V110411 | (S,R,S)-AHPC-C2-PEG3-NH2 | 2243090-28-8 | (S,R,S)-AHPC-C2-PEG3-NH2 is an E3 ligase ligand-linker conjugate that can be used to synthesize PROTAC USP39 degrader-1. |
|
V87922 | (S,R,S)-AHPC-CO-C9-NH2 | 2349429-71-4 | (S,R,S)-AHPC-CO-C9-NH2 is a Von Hippel-Lindau (VHL) amino building block that can be used to synthesize the E3 ligase ligands required for PROTACs. |
|
V99933 | (S,R,S)-AHPC-CO-cyclohexane-C2 | (S,R,S)-AHPC-CO-cyclohexane-C2 is an E3 ubiquitin ligase ligand-adapter conjugate. | |
|
V99917 | (S,R,S)-AHPC-CO-cyclohexene-Bpin | SMARCA2/4-ligand-adaptor binder-5 is an E3 ubiquitin ligase ligand-adaptor binder. | |
|
V122243 | (S,R,S)-AHPC-CO-PEG-C2-iodine | 3057447-11-4 | (S,R,S)-AHPC-CO-PEG-C2-iodine is an E3 ligase (VHL) ligand-linker conjugate that can be used to synthesize PROTACs, such as PROTAC FAK degrader 1. |
|
V122248 | (S,R,S)-AHPC-Me-amide-C-O-C5-Br | (S,R,S)-AHPC-Me-amide-CO-C5-Br contains a VHL ligand for an E3 ubiquitin ligase and a PROTAC linker. | |
|
V104243 | (S,R,S)-AHPC-Me-amide-C9-acid | 2376139-66-9 | (S,R,S)-AHPC-Me-amide-C9-acid is an E3 ligase ligand-linker conjugate used in the synthesis of PROTAC SMARCA2 degrader-31. |
|
V114022 | (S,R,S)-AHPC-Me-C4-NH2 hydrochloride | 2458219-89-9 | (S,R,S)-AHPC-Me-C4-NH2 hydrochloride is an E3 ligand-linker conjugate comprising a VHL ligand and a linker based on (S,R,S)-AHPC. |
|
V97358 | (S,R,S)-AHPC-O-CF3-CO-cyclohexene-Bpin | (S,R,S)-AHPC-O-CF3-CO-cyclohexene-Bpin is an E3 ubiquitinase ligand + adaptor conjugate. | |
|
V82360 | (−)-N-Hydroxyapiosporamide (NHAP) | 1205676-02-3 | (−)-N-Hydroxyapiosporamide (NHAP) is an alkaloid and an NF-κB inhibitor (antagonist) with potent anticancer effect in vitro and in vivo. |
|
V112588 | 2-(2,6-Dioxopiperidin-3-yl)phthalimidine-O-piperidine | 2222115-81-1 | 2-(2,6-dioxadiazine-3-yl)phthalimide-O-piperidine is an E3 ligand-linker conjugate containing a CRBN ligand and a linker, which can be used to synthesize PROTAC. |
|
V113107 | 2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine dihydrochloride | 2369981-22-4 | 2-(2,6-dioxadiazin-3-yl)phthalimide-piperazine-piperidine dihydrochloride is an E3 ligand-linker conjugate containing a CRBN-based ligand and a linker, which can be used to synthesize PROTAC. |
|
V112965 | 6-(2,6-Dioxopiperidin-3-yl)-2-(piperazin-1-yl)-5H-pyrrolo[3,4-d]pyrimidine-5,7(6H)-dione hydrochloride | 2229738-21-8 | 6-(2,6-dioxadiazin-3-yl)-2-(piperazin-1-yl)-5H-pyrrolo[3,4-d]pyrimidine-5,7(6H)-dione hydrochloride is an E3 ligand-linker conjugate containing a CRBN ligand and a linker, which can be used to synthesize PROTAC. |
|
V97421 | Ac-NH-(S,R,S)-AHPC-CO-cyclohexane-pyrimidine-diazabicyclo | Ac-NH-(S,R,S)-AHPC-CO-cyclohexane-pyrimidine-diazabicyclo is an E3 ligase ligand-linker conjugate. | |
|
V82339 | Alkaline phosphatase (alkaline phosphatase; Apase) | 9001-78-9 | Alkaline phosphatase (Apase) is a membrane-bound glycoprotein that catalyzes the hydrolysis of phosphate monoesters at alkaline pH. |
|
V82346 | ALV2 | 2438124-95-7 | ALV2 is a potent and specific Helios degrader. |
|
V82362 | Amino-PEG7-t-butyl ester | 2428400-07-9 | Amino-PEG7-t-butyl ester is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V82487 | Azido-PEG4-azide | 182760-73-2 | Azido-PEG4-azide is a PROTAC (PROteolysis TArgeting Chimera) linker and belongs to the PEG (Polyethylene glycol) class. |
|
V82469 | Benzyl-PEG12-alcohol | 2218463-17-1 | Benzyl-PEG12-alcohol is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |