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Results for "

hydroxy peg12 acid

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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Hydroxy-PEG12-acid
T18034
Hydroxy-PEG12-acid, a PEG-based linker for PROTACs, 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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Hydroxy-PEG10-acid
T180312375611-66-6
Hydroxy-PEG10-acid (HO-PEG10-CH2CH2COOH) is a PEG-based PROTAC linker that can be used to synthesize PROTACs[1].
  • $29
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Cbz-NH-PEG12-C2-acid
T177191334177-88-6
Cbz-NH-PEG12-C2-acid is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands to form PROTAC molecules, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
  • $53
In Stock
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Hydroxy-PEG12-Boc
T180352388521-20-6
Hydroxy-PEG12-Boc (Hydroxy-PEG12-T-Butyl Ester) is a PEG-based PROTAC linker. Hydroxy-PEG12-Boc can be used in the synthesis of PROTACs.
  • $34
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Azido-PEG12-acid
T174842152679-71-3
Azido-PEG12-acid (PROTAC Linker 13) is a polyethylene glycol-based linker utilized in the synthesis of PROTACs.
  • $41
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Amino-PEG12-acid
T174051415408-69-3
Amino-PEG12-acid, a PEG-based PROTAC linker, is utilized in PROTAC synthesis.
  • $61
In Stock
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m-PEG12-acid
T181322135793-73-4
m-PEG12-acid is a PEG-based PROTAC linker used in the synthesis of PROTACs.
  • $32
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TargetMol | Inhibitor Sale
SPDP-PEG12-acid
T18709
SPDP-PEG12-acid, a cleavable 12-unit polyethylene glycol (PEG) linker, is used for the synthesis of antibody-drug conjugates (ADCs)[1].
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DNP-PEG12-acid
T17837
DNP-PEG12-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Mal-amido-PEG12-acid
T182362378428-27-2
Mal-amido-PEG12-acid is a PEG-based linker for PROTACs, facilitating the formation of PROTAC molecules by connecting two essential ligands and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
  • $35
2-4 weeks
Size
QTY
endo-BCN-PEG12-acid
T17932
endo-BCN-PEG12-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Fmoc-aminooxy-PEG12-acid
T17947
Fmoc-aminooxy-PEG12-acid, a PEG-based PROTAC linker, is employed for synthesizing PROTACs[1].
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Hydroxy-PEG4-acid
T15528937188-59-5
Hydroxy-PEG4-acid, a non-cleavable 4-unit PEG ADC linker, is utilized in the synthesis of antibody-drug conjugates (ADCs) [1].
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7-10 days
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Biotin-PEG12-acid
T145811621423-14-0
Biotin-PEG12-acid is a PEG-based PROTAC linker labeled with biotin, designed for synthesis of PROTACs[1].
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DBCO-PEG12-acid
T17782
DBCO-PEG12-acid is a PEG-based linker for PROTACs that connects two essential ligands, enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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Hydroxy-PEG1-acid
T1551089211-34-7
Hydroxy-PEG1-acid is a non-cleavable 1-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
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7-10 days
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Hydroxy-PEG5-acid
T394832079768-50-4
Hydroxy-PEG5-acid is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
  • $30
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Thiol-PEG12-acid
T188362211174-73-9
Thiol-PEG12-acid, a PEG-based linker for PROTACs, joins two essential ligands necessary for PROTAC molecule formation and facilitates selective protein degradation through the ubiquitin-proteasome system within cells.
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Hydroxy-PEG2-acid
T155151334286-77-9
Hydroxy-PEG2-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
  • Inquiry Price
7-10 days
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Lipoamido-PEG12-acid
T180732407442-47-9
Lipoamido-PEG12-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Hydroxy-PEG6-acid
T155361347750-85-9
Hydroxy-PEG6-acid is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
  • $30
5 days
Size
QTY
TCO-PEG12-acid
T19575
TCO-PEG12-acid is a PROTAC connection bridge, belonging to the PEG class. TCO-PEG12-acid can be used to synthesize a series of PROTAC molecules.
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Mal-PEG12-acid
T182702445165-75-1
Mal-PEG12-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Hydroxy-PEG3-acid
T20849518044-49-0
Hydroxy-PEG3-acid is a PEG derivative containing a hydroxyl group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functi
  • Inquiry Price
7-10 days
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Hydroxy-PEG12-CH2-Boc
T18036
Hydroxy-PEG12-CH2-Boc is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This compound facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Fmoc-12-aminododecanoic acid
T71967128917-74-8
Fmoc-12-aminododecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
  • $1,520
6-8 weeks
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m-PEG8-(CH2)12-phosphonic acid ethyl ester
T159312112737-70-7
m-PEG8-(CH2)12-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-based PROTAC linker, ideal for synthesizing PROTAC compounds[1].
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Amino-SS-PEG12-acid
T17443
Amino-SS-PEG12-acid, a cleavable 12-unit polyethylene glycol (PEG) linker, is commonly used in the synthesis of antibody-drug conjugates (ADCs)[1].
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t-Boc-Aminooxy-PEG12-acid
T18738
t-Boc-Aminooxy-PEG12-acid is a polyethylene glycol (PEG)-based PROTAC linker used for synthesizing PROTACs [1].
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Iodo-PEG12-acid
T18050
Iodo-PEG12-acid is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands to form PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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N-(Propanoic acid)-N-bis(m-PEG12)
T18462
N-(Propanoic acid)-N-bis(m-PEG12) is a polyethylene glycol (PEG) based linker used in PROTACs synthesis [1].
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Hydroxy-PEG2-C2-sulfonic acid
T15518112724-27-3
Hydroxy-PEG2-C2-sulfonic acid, a PEG-based linker for PROTACs, connects two essential ligands critical for forming PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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m-PEG12-COO-propanoic acid
T181362168540-50-7
m-PEG12-COO-propanoic acid is a polyethylene glycol (PEG) derivative used as a PROTAC linker for synthesizing PROTAC compounds [1].
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Bis-PEG12-acid
T17615
Bis-PEG12-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Hydroxy-PEG16-acid
T18038
Hydroxy-PEG16-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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m-PEG12-NH-C2-acid
T181411949843-39-3
m-PEG12-NH-C2-acid is a PEG-based linker for PROTACs, joining two essential ligands necessary for the formation of PROTAC molecules. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system [within cells].
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