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Methyltetrazine-amino-PEG3-CH2CH2NHBoc

  CAS No.: 2141976-32-9   Cat No.: BADC-01959   Purity: >95% 4.5  

Methyltetrazine-amino-PEG3-CH2CH2NHBoc provides a shorter PEG spacer ADC linker with methyltetrazine functionality, facilitating efficient and selective antibody conjugation in ADC synthesis.

Methyltetrazine-amino-PEG3-CH2CH2NHBoc

Structure of 2141976-32-9

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Category
ADC Linker
Molecular Formula
C24H36N6O6
Molecular Weight
504.587
Storage
Store at -18°C

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

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Synonyms
Me-Tet-PEG3-NHBoc; Methyltetrazine-amino-PEG3-CH2CH2NHBoc; 2141976-32-9; HY-156479; CS-0903621; Methyltetrazine-CH2NHCO-PEG3-CH2CH2NHBoc
IUPAC Name
tert-butyl N-[2-[2-[2-[3-[[4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl]methylamino]-3-oxopropoxy]ethoxy]ethoxy]ethyl]carbamate
Canonical SMILES
CC1=NN=C(N=N1)C2=CC=C(C=C2)CNC(=O)CCOCCOCCOCCNC(=O)OC(C)(C)C
InChI
InChI=1S/C24H36N6O6/c1-18-27-29-22(30-28-18)20-7-5-19(6-8-20)17-26-21(31)9-11-33-13-15-35-16-14-34-12-10-25-23(32)36-24(2,3)4/h5-8H,9-17H2,1-4H3,(H,25,32)(H,26,31)
InChIKey
SCIOKEISYHYNHO-UHFFFAOYSA-N
Storage
Store at -18°C

Methyltetrazine-amino-PEG3-CH2CH2NHBoc, a versatile chemical compound utilized in bioconjugation and chemical biology research, plays a pivotal role in various applications.

Bioorthogonal Chemistry: Positioned at the forefront of bioorthogonal chemistry, Methyltetrazine-amino-PEG3-CH2CH2NHBoc serves as a cornerstone for labeling biomolecules within living systems. Its interaction with trans-cyclooctene (TCO) derivatives triggers rapid and specific conjugation reactions in physiological surroundings. This unique feature is paramount in imaging endeavors, enabling scientists to trace biomolecules without disrupting cellular processes.

Drug Delivery Systems: At the intersection of chemistry and medicine, this compound contributes to the development of targeted drug delivery systems by conjugating therapeutic agents to specific targeting molecules. Acting as a pivotal linking group, Methyltetrazine facilitates controlled drug release through click reactions with TCO-functionalized carriers. This precision enhances drug delivery efficiency, ultimately improving therapeutic outcomes.

Protein Modification: Within the realm of protein modification, Methyltetrazine-amino-PEG3-CH2CH2NHBoc plays a crucial role in site-specific labeling of proteins for structural and functional studies. By selectively reacting with appropriately modified proteins, it enables the incorporation of fluorescent probes or other functional groups. This capability is instrumental in unraveling protein interactions, localization, and dynamics within cellular contexts, shedding light on intricate molecular processes.

Antibody Conjugation: Offering a solution in targeted therapy, this compound’s stable linkages with antibodies make it an ideal candidate for antibody-drug conjugates (ADCs). Leveraging bioorthogonal chemistry principles, Methyltetrazine-amino-PEG3-CH2CH2NHBoc facilitates precise attachment of cytotoxic drugs to antibodies. This targeted approach is indispensable for designing cancer therapies that deliver drugs exclusively to cancer cells, minimizing collateral damage and off-target effects.

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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