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Results for "
boc nh peg3
" in TargetMol Product Catalog- Inhibitors & Agonists20
- PROTAC Products19
Boc-NH-PEG3
PROTAC Linker 10
T7701139115-92-7
Boc-NH-PEG3 (PROTAC Linker 10) is a PEG derivative featuring a hydroxyl group and a Boc-protected amino group, used as a PROTAC linker.
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Boc-NH-PEG3-NHS ester
T176772250216-93-2
Boc-NH-PEG3-NHS ester is a PEG-based linker utilized in the synthesis of PROTACs.
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Boc-NH-PEG3-CH2COOH
T14741462100-06-7
Boc-NH-PEG3-CH2COOH, a PEG-based PROTAC linker, can be utilized in PROTAC synthesis [1].
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Ald-Ph-amido-C2-PEG3-NH-Boc
T141631807540-87-9
Ald-Ph-amido-C2-PEG3-NH-Boc is a polyethylene glycol (PEG)-based bifunctional linker used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
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Aminooxy-PEG3-C2-NH-Boc
T142672062663-65-2
Aminooxy-PEG3-C2-NH-Boc is a PEGylated PROTAC linker used in synthesizing PROTACs, a new class of bifunctional molecules for targeted protein degradation [1].
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Boc-NH-PEG3-propargyl
T147421333880-60-6
Boc-NH-PEG3-propargyl is a PEG-based linker used in PROTACs for connecting two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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Boc-NH-PEG3-sulfonic acid
T147431817735-32-2
Boc-NH-PEG3-sulfonic acid, a polyethylene glycol (PEG) derived linker, is utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
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Bromoacetamido-PEG3-NH-Boc
T148221421933-39-2
Bromoacetamido-PEG3-NH-Boc is a polyethylene glycol (PEG)-based linker compound used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
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endo-BCN-PEG3-NH-Boc
T152251807501-84-3
endo-BCN-PEG3-NH-Boc is a PEG-based linker for PROTACs, joining two essential ligands integral to PROTAC molecule formation, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
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Fluorescein-PEG3-NH-Boc
T152921807534-77-5
Fluorescein-PEG3-NH-Boc is a polyethylene glycol (PEG)-based proteolysis-targeting chimera (PROTAC) linker used for PROTAC synthesis[1].
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NH-bis(PEG3-Boc)
T163031814901-03-5
NH-bis(PEG3-Boc) is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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NH-bis(PEG3-C2-NH-Boc)
T163042055024-51-4
NH-bis(PEG3-C2-NH-Boc) is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA
T17676
Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA is a double-cleavable PEG linker (3-unit and 4-unit) designed for antibody-drug conjugation (ADC).
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Fmoc-N-bis-PEG3-NH-Boc
T17956
Fmoc-N-bis-PEG3-NH-Boc is a cleavable ADC linker compound with three PEG units, used in the synthesis of antibody-drug conjugates (ADCs)[1].
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N-(Azido-PEG3)-N-(PEG2-NH-Boc)-PEG3-acid
T183842183440-74-4
N-(Azido-PEG3)-N-(PEG2-NH-Boc)-PEG3-acid is a polyethylene glycol (PEG)-based linker used in the development of proteolysis targeting chimeras (PROTACs)[1].
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Tos-PEG3-NH-Boc
PROTAC Linker 9
T18630206265-94-3
Tos-PEG3-NH-Boc (PROTAC Linker 9) is a PEG-based linker used in the synthesis of PROTACs, which connects a target protein with an E3 ubiquitin ligase to promote the target protein's degradation.
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Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc
Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc
T392161799711-31-1
Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc is a synthesized conjugate functioning as an E3 ligase ligand-linker, incorporating the cereblon ligand derived from Thalidomide and a linker, and is utilized in the synthesis of PROTAC BET degraders.
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NH2-PEG3-C1-Boc
PROTAC Linker 5
T16666189808-70-6
NH2-PEG3-C1-Boc, also known as PROTAC Linker 5, is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1].
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NH2-PEG3-C2-Boc
Amino-PEG3-t-butyl ester
T20098252881-74-6
Amino-PEG3-t-butyl ester is a PEG derivative containing an amino group with the t-butyl protected carboxyl group. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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