2-Ethyl-3-methylmaleimide N-β-D-glucopyranoside

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Reagent Code: #184754
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CAS Number 182228-46-2

science Other reagents with same CAS 182228-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.29 g/mol
Formula C₁₃H₁₉NO₇
thermostat Physical Properties
Boiling Point 539.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.504±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a glycosylation reagent in medicinal chemistry to improve the solubility and bioavailability of drug candidates. It serves as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents by combining the targeting ability of antibodies with the potency of small molecule drugs. Its maleimide group allows for selective conjugation with thiol groups via Michael addition, while the glucopyranoside moiety enhances water solubility and reduces immunogenicity. Also employed in the development of glycoconjugate vaccines and in biochemical research for labeling and detecting biomolecules.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿61,750.00

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2-Ethyl-3-methylmaleimide N-β-D-glucopyranoside
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Used as a glycosylation reagent in medicinal chemistry to improve the solubility and bioavailability of drug candidates. It serves as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents by combining the targeting ability of antibodies with the potency of small molecule drugs. Its maleimide group allows for selective conjugation with thiol groups via Michael addition, while the glucopyranoside moiety enhances water solubility and reduces immunogenicity. Also employe

Used as a glycosylation reagent in medicinal chemistry to improve the solubility and bioavailability of drug candidates. It serves as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents by combining the targeting ability of antibodies with the potency of small molecule drugs. Its maleimide group allows for selective conjugation with thiol groups via Michael addition, while the glucopyranoside moiety enhances water solubility and reduces immunogenicity. Also employed in the development of glycoconjugate vaccines and in biochemical research for labeling and detecting biomolecules.

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