cas 1569261-93-3|| where to buy Mal-PEG4-VC-PAB-DMEA

Nombre del producto:Mal-PEG4-VC-PAB-DMEA

IUPAC Name:{4-[(2S)-5-(carbamoylamino)-2-[(2S)-2-{1-[3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanamido]-3,6,9,12-tetraoxapentadecan-15-amido}-3-methylbutanamido]pentanamido]phenyl}methyl N-methyl-N-[2-(methylamino)ethyl]carbamate

: CAS：1569261-93-3; Fórmula molecular：C41H65N9O13; Pureza：95%+

: Número de catálogo：CM339133; Peso molecular：892.02

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: Núm. De CAS :1569261-93-3; Fórmula molecular:C41H65N9O13; Punto de fusión:-; Código de sonrisas:O=C(C=CC1=O)N1CCC(NCCOCCOCCOCCOCCC(N[C@@H](C(C)C)C(N[C@@H](CCCNC(N)=O)C(NC(C=C2)=CC=C2COC(N(C)CCNC)=O)=O)=O)=O)=O; Densidad:

: Número de catálogo:CM339133; Peso molecular:892.02; Punto de ebullición:; Nº Mdl:; Almacenamiento:

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: ADC-Linkers; The ADC linker is one of the three main components of antibody drug conjugates (ADCs), linking the antibody to the effective drug (payload) through chemical bonds. ADC linkers play a key role in determining the overall success of antibody drug conjugates. One of the major challenges in developing safe and effective ADC drugs is to assemble an ideal chemical linker between the cytotoxic payload and the mAb. Well-designed ADC linkers can help the selective delivery of antibodies at the tumor site and the accurate release of cytotoxic drugs.

: Cleavable linkers; Cleavable linkers rely on the inherent properties of a cell’s cytoplasmic compartments for selective release of the cytotoxic drug.

: Peptide linkers; Peptide linkers belong to protease-sensitivity linkers (also called enzymatically cleavable linkers) that have gained significant attention in ADC development due to their superior plasma stability and controled payload release mechanism.

: PEG linkers; PEG Reagents are chemically functionalized polyethylene glycol (PEG) linkers.PEG linkers are highly water-soluble and non-immunogenic linkers.

: Maleimides; Thiol-maleimide is a bifunctional chemical compound that is commonly used in bioconjugation reactions to crosslink two molecules via the thiol (-SH) groups.

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