1-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-3-oxo-7,10,13,16,19,22-hexaoxa-4-azapentacosan-25-oic acid

98%

Reagent Code: #177624
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CAS Number 1334177-79-5

science Other reagents with same CAS 1334177-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.53 g/mol
Formula C₂₂H₃₆N₂O₁₁
badge Registry Numbers
MDL Number MFCD21363276
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in bioconjugation processes, particularly in the preparation of antibody-drug conjugates (ADCs) and other targeted therapeutics. Its structure contains a maleimide group that selectively reacts with thiol groups (–SH) on cysteine residues of proteins, enabling stable linkage between biomolecules and functional payloads. The long, hydrophilic polyethylene glycol (PEG) spacer improves solubility, reduces aggregation, and enhances the pharmacokinetic properties of the conjugated molecules. The terminal carboxylic acid allows for further activation and coupling to amines, making it useful for multi-step conjugation strategies. Commonly employed in pharmaceutical research and development for creating highly specific, effective biopharmaceuticals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,090.00
inventory 250mg
10-20 days ฿8,670.00
inventory 1g
10-20 days ฿23,310.00

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1-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-3-oxo-7,10,13,16,19,22-hexaoxa-4-azapentacosan-25-oic acid
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Used in bioconjugation processes, particularly in the preparation of antibody-drug conjugates (ADCs) and other targeted therapeutics. Its structure contains a maleimide group that selectively reacts with thiol groups (–SH) on cysteine residues of proteins, enabling stable linkage between biomolecules and functional payloads. The long, hydrophilic polyethylene glycol (PEG) spacer improves solubility, reduces aggregation, and enhances the pharmacokinetic properties of the conjugated molecules. The terminal

Used in bioconjugation processes, particularly in the preparation of antibody-drug conjugates (ADCs) and other targeted therapeutics. Its structure contains a maleimide group that selectively reacts with thiol groups (–SH) on cysteine residues of proteins, enabling stable linkage between biomolecules and functional payloads. The long, hydrophilic polyethylene glycol (PEG) spacer improves solubility, reduces aggregation, and enhances the pharmacokinetic properties of the conjugated molecules. The terminal carboxylic acid allows for further activation and coupling to amines, making it useful for multi-step conjugation strategies. Commonly employed in pharmaceutical research and development for creating highly specific, effective biopharmaceuticals.

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