Inhibitor
| Cat.No. | Name | Information |
|---|---|---|
| M57091 | (S,R,S)-AHPC-C3-NH2 dihydrochloride | (S,R,S)-AHPC-C3-NH2 (dihydrochloride) is the dihydrochloride form of (S,R,S)-AHPC-C3-NH2. |
| M57090 | (S,R,S)-AHPC-C7-amine hydrochloride | (S,R,S)-AHPC-C7-amine (VH032-C7-amine) hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used for estrogen-related receptor α (ERRα) PROTAC degrader. |
| M57089 | (S,R,S)-AHPC-C8-NH2 dihydrochloride | (S,R,S)-AHPC-C8-NH2 dihydrochloride (VH032-C8-NH2 dihydrochloride) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used for AKT PROTAC degrader. |
| M57088 | Boc-A 410099.1 amide-alkylC4-amine | Boc-A 410099.1 amide-alkylC4-amine is a functionalized IAP ligand for PROTACs that incorporates an IAP ligand and an amide-alkylC4 linker with terminal amine. |
| M57087 | (S,R,S)-AHPC-C7-amine dihydrochloride | (S,R,S)-AHPC-C7-amine dihydrochloride is the dihydrochloride form of (S,R,S)-AHPC-C7-amine. |
| M57086 | Thalidomide-O-amido-PEG4-C2-NH2 hydrochloride | Thalidomide-O-amido-PEG4-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker, can be used in the synthesis of PROTACs. |
| M57085 | (S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride | (S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and an alkyl linker used for PROTAC degrader. |
| M43410 | Cereblon inhibitor 2 | Cereblon inhibitor 2 is a Cereblon inhibitor useful in solid tumor research, especially breast cancer. |
| M43409 | Pomalidomide-C7-NH2 hydrochloride | Pomalidomide-C7-NH2 (Pomalidomide 4'-alkylC7-amine) hydrochloride is an E3 ligase ligand-linker conjugate. |
| M31273 | Thalidomide-NH-PEG2-C2-NH-Boc | Thalidomide-NH-PEG2-C2-NH-Boc is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a PEG linker used for dBRD9 synthesis. dBRD9 is a selective BRD9 probe PROTAC degrader for the study of BAF complex biology. |
| M31272 | Thalidomide-C2-amido-C2-COOH | Thalidomide-C2-amido-C2-COOH incorporates a CRBN ligand for the E3 ubiquitin ligase, and a linker. Thalidomide-C2-amido-C2-COOH can be used to design PROTAC CDK2/9 Degrader-1. |
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