E3 Ligase Ligand-Linker Conjugate
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E3 Ligase Ligand-Linker Conjugate, which is one part of Proteolysis Targeting Chimeric Molecules (PROTACs), incorporates a ligand for the E3 ubiquitin ligase and a linker. After linked to the ligand for target protein (such as JQ1 for BRD4 protein, Molibresib for BET protein), those conjugates can be used for constituting PROTACs that targetprotein for ubiquitination and degradation. Currently, several PROTACs have been found to show good biological activity by specifically targeting BET, estrogen receptor (ER), androgen receptor, etc.MedChemExpress (MCE) offers a wide range of high quality E3 Ligase Ligand-Linker Conjugates including von Hippel-Lindau (VHL) ligands, MDM2 ligands, Cereblon (CRBN) ligands and cIAP1 ligands conjugating with different linkers (PEGs, Alkyl-Chain, Alkyl/ether, etc.). It’s convenient and time-saving for designing and synthesizinga wide variety of novel PROTACs (ARV-825, dBET1,MT-802, etc.), which can expand the application of PROTACs in the treatment of cancer, autoimmunity, inflammation and other diseases.
Products Related to E3 Ligase Ligand-Linker Conjugate(201)
- GC35956E3 ligase Ligand-Linker Conjugates 49CAS: 2351103-63-2Purity: >98%
E3 ligase Ligand-Linker Conjugates 49 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology.
- GC38095Thalidomide-O-amido-C3-NH2 (TFA)CAS: 2022182-58-5Purity: >98.00%
Thalidomide-O-amido-C3-NH2 (TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
- GC38381Pomalidomide-C2-NH2 hydrochlorideCAS: 2305369-00-8Purity: >98%
Pomalidomide-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology.
- GC38808Lenalidomide-propargyl-C2-NH2 hydrochlorideCAS: 2489242-23-9Purity: >99.00%
Lenalidomide-propargyl-C2-NH2 hydrochloride incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Lenalidomide-propargyl-C2-NH2 hydrochloride can be used to design the PROTAC MD-224.
- GC38861Thalidomide-O-PEG2-propargylCAS: 2098487-52-4Purity: >98%
Thalidomide-O-PEG2-propargyl (E3 ligase Ligand-Linker Conjugates 32) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology.
- GC38870VH032-PEG3-acetyleneCAS: 2098799-80-3Purity: >98%
VH032-PEG3-acetylene is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in PROTAC technology.
- GC38949Thalidomide-NH-PEG2-C2-NH2 TFACAS: 2097509-36-7Purity: >98.50%
Thalidomide-NH-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology.
- GC39171Pomalidomide-amido-C1-BrCAS: 2351106-38-0Purity: >98%
Pomalidomide-amido-C1-Br is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker. Pomalidomide-amido-C1-Br can be used to design a B-Raf PROTAC degrader PROTAC B-Raf degrader 1. PROTAC B-Raf degrader 1 has anti-cancer activity.
- GC39513Thalidomide-NH-C6-NH2 TFACAS: 2093386-51-5Purity: >99.50%
Thalidomide-NH-C6-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
- GC50463Thalidomide 4'-oxyacetamide-PEG4-amineCAS: 2245697-85-0Purity: >98%
Thalidomide 4'-oxyacetamide-PEG4-amine, 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.
- GC50466A 410099.1, amineCAS: 2374122-37-7Purity: >98%
A 410099.1, amine is afunctionalizedIAP ligand and can be used for the synthesis of PROTACs, such as PROTACs targeting BTK (PROTACs 4 and 5).
- GC50528Thalidomide 4'-ether-alkylC6-amineCAS: 2245697-88-3Purity: >98.50%
Thalidomide 4'-ether-alkylC6-amine is a synthesized E3 ligase ligand-linker conjugate used in the PROTAC dTAG-13, a degrader of FKBP12F36V and BET.
- GC50545Pomalidomide 4'-PEG3-acidCAS: 2138440-82-9Purity: >98.50%
Pomalidomide 4'-PEG3-acid is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
- GC50583Thalidomide 4'-ether-alkylC2-amineCAS: 2341840-99-9Purity: >98%
Thalidomide 4'-ether-alkylC2-amine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
- GC50584VH 032 amide-alkylC2-amineCAS: 2341796-73-2Purity: >98.50%
VH 032 amide-alkylC2-amine incorporates a VHL ligand for the E3 ubiquitin ligase, and a PROTAC linker. (S,R,S)-AHPC-OH can be used in the synthesis of a series of PROTACs.
- GC50585VH 032 amide-alkylC6-amineCAS: 2341796-77-6Purity: >98%
VH 032 amide-alkylC6-amine (VH032-C6-NH2 dihydrochloride) is a synthesizedE3 ligase ligand-linker conjugatethat incorporates the VH032 based VHL ligand and a linker used forAKTPROTAC degrader.
- GC50592VH 032 amide-alkylC10-amineCAS: 2341796-75-4Purity: >98%
VH 032 amide-alkylC10-amine (VH032-C10-NH2 dihydrochloride) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and a linker used for BET-Targeted PROTAC.
- GC50620Thalidomide 4'-oxyacetamide-alkylC2-amineCAS: 2341841-02-7Purity: >98%
Thalidomide 4'-oxyacetamide-alkylC2-amine incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Thalidomide 4'-oxyacetamide-alkylC2-amine can be used to design the PROTACs.
- GC50622Thalidomide 4'-ether-PEG5-amineCAS: 2341841-01-6Purity: >98%
Cereblon ligand with PEG linker and terminal amine for onward chemistry
- GC50626Thalidomide 4'-oxyacetamide-PEG1-amineCAS: 2204226-02-6Purity: >98.50%
Thalidomide 4'-oxyacetamide-PEG1-amine, 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.
- GC50657Thalidomide 4'-ether-alkylC2-acidCAS: 2369068-42-6Purity: >95.00%
Thalidomide 4'-ether-alkylC2-acid is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC35955 | E3 ligase Ligand-Linker Conjugates 48 | - | >98% | |
| GC35956 | E3 ligase Ligand-Linker Conjugates 49 | 2351103-63-2 | >98% | |
E3 ligase Ligand-Linker Conjugates 49 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
| GC35957 | E3 ligase Ligand-Linker Conjugates 50 | - | >98% | |
| GC35958 | E3 ligase Ligand-Linker Conjugates 51 | - | >98% | |
| GC38095 | Thalidomide-O-amido-C3-NH2 (TFA) | 2022182-58-5 | >98.00% | |
Thalidomide-O-amido-C3-NH2 (TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
| GC38381 | Pomalidomide-C2-NH2 hydrochloride | 2305369-00-8 | >98% | |
Pomalidomide-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
| GC38808 | Lenalidomide-propargyl-C2-NH2 hydrochloride | 2489242-23-9 | >99.00% | |
Lenalidomide-propargyl-C2-NH2 hydrochloride incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Lenalidomide-propargyl-C2-NH2 hydrochloride can be used to design the PROTAC MD-224. | ||||
| GC38861 | Thalidomide-O-PEG2-propargyl | 2098487-52-4 | >98% | |
Thalidomide-O-PEG2-propargyl (E3 ligase Ligand-Linker Conjugates 32) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology. | ||||
| GC38870 | VH032-PEG3-acetylene | 2098799-80-3 | >98% | |
VH032-PEG3-acetylene is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in PROTAC technology. | ||||
| GC38949 | Thalidomide-NH-PEG2-C2-NH2 TFA | 2097509-36-7 | >98.50% | |
Thalidomide-NH-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology. | ||||
| GC39171 | Pomalidomide-amido-C1-Br | 2351106-38-0 | >98% | |
Pomalidomide-amido-C1-Br is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker. Pomalidomide-amido-C1-Br can be used to design a B-Raf PROTAC degrader PROTAC B-Raf degrader 1. PROTAC B-Raf degrader 1 has anti-cancer activity. | ||||
| GC39513 | Thalidomide-NH-C6-NH2 TFA | 2093386-51-5 | >99.50% | |
Thalidomide-NH-C6-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
| GC50463 | Thalidomide 4'-oxyacetamide-PEG4-amine | 2245697-85-0 | >98% | |
Thalidomide 4'-oxyacetamide-PEG4-amine, 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. | ||||
| GC50466 | A 410099.1, amine | 2374122-37-7 | >98% | |
A 410099.1, amine is afunctionalizedIAP ligand and can be used for the synthesis of PROTACs, such as PROTACs targeting BTK (PROTACs 4 and 5). | ||||
| GC50528 | Thalidomide 4'-ether-alkylC6-amine | 2245697-88-3 | >98.50% | |
Thalidomide 4'-ether-alkylC6-amine is a synthesized E3 ligase ligand-linker conjugate used in the PROTAC dTAG-13, a degrader of FKBP12F36V and BET. | ||||
| GC50545 | Pomalidomide 4'-PEG3-acid | 2138440-82-9 | >98.50% | |
Pomalidomide 4'-PEG3-acid is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology. | ||||
| GC50583 | Thalidomide 4'-ether-alkylC2-amine | 2341840-99-9 | >98% | |
Thalidomide 4'-ether-alkylC2-amine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
| GC50584 | VH 032 amide-alkylC2-amine | 2341796-73-2 | >98.50% | |
VH 032 amide-alkylC2-amine incorporates a VHL ligand for the E3 ubiquitin ligase, and a PROTAC linker. (S,R,S)-AHPC-OH can be used in the synthesis of a series of PROTACs. | ||||
| GC50585 | VH 032 amide-alkylC6-amine | 2341796-77-6 | >98% | |
VH 032 amide-alkylC6-amine (VH032-C6-NH2 dihydrochloride) is a synthesizedE3 ligase ligand-linker conjugatethat incorporates the VH032 based VHL ligand and a linker used forAKTPROTAC degrader. | ||||
| GC50592 | VH 032 amide-alkylC10-amine | 2341796-75-4 | >98% | |
VH 032 amide-alkylC10-amine (VH032-C10-NH2 dihydrochloride) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and a linker used for BET-Targeted PROTAC. | ||||
| GC50620 | Thalidomide 4'-oxyacetamide-alkylC2-amine | 2341841-02-7 | >98% | |
Thalidomide 4'-oxyacetamide-alkylC2-amine incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Thalidomide 4'-oxyacetamide-alkylC2-amine can be used to design the PROTACs. | ||||
| GC50622 | Thalidomide 4'-ether-PEG5-amine | 2341841-01-6 | >98% | |
Cereblon ligand with PEG linker and terminal amine for onward chemistry | ||||
| GC50626 | Thalidomide 4'-oxyacetamide-PEG1-amine | 2204226-02-6 | >98.50% | |
Thalidomide 4'-oxyacetamide-PEG1-amine, 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. | ||||
| GC50657 | Thalidomide 4'-ether-alkylC2-acid | 2369068-42-6 | >95.00% | |
Thalidomide 4'-ether-alkylC2-acid is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. | ||||
