rel-2, 5-Dioxopyrrolidin-1-yl 1-((1R, 8S, 9s)-bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2, 7, 10, 13, 16-pentaoxa-4-azanonadecan-19-oate

97%

Reagent Code: #177913
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CAS Number 1702356-19-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.59 g/mol
Formula C₂₆H₃₈N₂O₁₀
badge Registry Numbers
MDL Number MFCD23704191
inventory_2 Storage & Handling
Storage -20°C, dry, away from light

description Product Description

Used as a cleavable linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents to cancer cells. The compound contains a strained alkyne group that participates in bioorthogonal click chemistry, allowing for selective conjugation under physiological conditions. Its dioxopyrrolidinyl ester functionality facilitates efficient coupling to antibodies or other biomolecules. The polyether chain provides hydrophilicity and flexibility, improving solubility and reducing aggregation in biological environments. Upon internalization into target cells, the linker can be cleaved under specific intracellular conditions, releasing the active drug payload. This makes it valuable in the development of precision oncology therapeutics with improved stability and controlled release profiles.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days $182.64
inventory 50mg
10-20 days $364.48
inventory 100mg
10-20 days $728.17
rel-2, 5-Dioxopyrrolidin-1-yl 1-((1R, 8S, 9s)-bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2, 7, 10, 13, 16-pentaoxa-4-azanonadecan-19-oate
Used as a cleavable linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents to cancer cells. The compound contains a strained alkyne group that participates in bioorthogonal click chemistry, allowing for selective conjugation under physiological conditions. Its dioxopyrrolidinyl ester functionality facilitates efficient coupling to antibodies or other biomolecules. The polyether chain provides hydrophilicity and flexibility, improving solubility and reducing aggregation in biological environments. Upon internalization into target cells, the linker can be cleaved under specific intracellular conditions, releasing the active drug payload. This makes it valuable in the development of precision oncology therapeutics with improved stability and controlled release profiles.
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