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2,5-dioxopyrrolidin-1-yl 1-(bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2,7,10-trioxa-4-azatridecan-13-oate

  CAS No.: 2243565-12-8   Cat No.: BADC-00419   Purity: 98% 4.5  

2,5-dioxopyrrolidin-1-yl 1-(bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2,7,10-trioxa-4-azatridecan-13-oate is a small molecule compound with biological activity. It has been widely studied as a linker in ADC development.

2,5-dioxopyrrolidin-1-yl 1-(bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2,7,10-trioxa-4-azatridecan-13-oate

Structure of 2243565-12-8

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Category
ADC Linker
Molecular Formula
C22H30N2O8
Molecular Weight
450.48
Shipping
Room temperature, or blue ice upon request.
Shipping
-20°C

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
endo-BCN-PEG2-OSu; endo-BCN-PEG2-NHS ester
IUPAC Name
(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-(9-bicyclo[6.1.0]non-4-ynylmethoxycarbonylamino)ethoxy]ethoxy]propanoate
Canonical SMILES
C1CC2C(C2COC(=O)NCCOCCOCCC(=O)ON3C(=O)CCC3=O)CCC#C1
InChI
InChI=1S/C22H30N2O8/c25-19-7-8-20(26)24(19)32-21(27)9-11-29-13-14-30-12-10-23-22(28)31-15-18-16-5-3-1-2-4-6-17(16)18/h16-18H,3-15H2,(H,23,28)
InChIKey
HVVMKCPRACMDSI-UHFFFAOYSA-N
Solubility
DMSO, DCM, DMF
Appearance
Soild powder
Shipping
Room temperature, or blue ice upon request.
Storage
-20°C

Pharmaceutical Development: This compound has shown promise in pharmaceutical development, particularly in the synthesis of new drug candidates. Its unique structural properties allow for modifications that enhance bioactivity and selectivity. As a potential lead compound, it can be optimized to improve therapeutic efficacy against various diseases, including cancer and infectious conditions. The ability to modify its chemical structure opens avenues for creating targeted therapies that minimize side effects while maximizing treatment benefits.

Material Science Applications: In material science, 2,5-dioxopyrrolidin-1-yl 1-(bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2,7,10-trioxa-4-azatridecan-13-oate serves as a precursor for developing advanced polymers. Its incorporation into polymer matrices enhances mechanical properties and thermal stability. Such materials find applications in coatings, adhesives, and various composite materials where performance under stress is critical. This compound’s versatility enables the formulation of materials tailored for specific industrial applications, contributing to innovations in product design and functionality.

Agrochemical Applications: The compound also has potential applications in agrochemicals, particularly as a pesticide or herbicide. Its structural characteristics may enable it to interact effectively with biological targets in pests and weeds, leading to enhanced pest management solutions. By optimizing its efficacy and reducing environmental impact, formulations derived from this compound can support sustainable agricultural practices. This aligns with the growing demand for eco-friendly agricultural solutions that balance productivity with ecological preservation.

Diagnostics and Imaging: Lastly, this compound can play a significant role in diagnostics and imaging technologies. Its chemical properties allow for conjugation with imaging agents, enhancing the contrast in various imaging modalities, such as MRI or PET scans. This capability can improve the detection and monitoring of diseases, offering better diagnostic tools for healthcare professionals. The development of targeted imaging agents that incorporate this compound could lead to advancements in early disease detection, personalized treatment planning, and improved patient outcomes.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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Historical Records: 2,5-dioxopyrrolidin-1-yl 1-(bicyclo[6.1.0]non-4-yn-9-yl)-3-oxo-2,7,10-trioxa-4-azatridecan-13-oate
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