ala-ala-asn-pab

Ala-Ala-Asn-PAB is a cleavable peptide linker employed in antibody-drug conjugates (ADCs), improving the physicochemical properties and toxicity profiles of cytotoxic drugs by forming stable peptide-drug conjugates, and facilitating controlled drug release in targeted therapies.

Ala-Ala-Asn-PAB TFA serves as a cleavable peptide linker for antibody-drug conjugates (ADCs) [1].

Azido-PEG5-Ala-Ala-Asn-PAB is a cleavable 5-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-PEG4-Ala-Ala-Asn-PAB is a cleavable four-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

MC-Ala-Ala-Asn-PAB serves as a linker and is utilized in synthesizing tumor microenvironment-specific activated micromolecular targeted conjugates [1].

Fmoc-Ala-Ala-Asn-PABC-PNP is a cleavable peptide ADC linker [1].

Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB is a cleavable three-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Azido-PEG4-Ala-Ala-Asn(Trt)-PAB is a PEG derivative conjugated with a peptide via an amide bond. The azide group on the PEG end enables Click Chemistry. The hydrophilic PEG spacer increases solubility in aqueous media.

Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP is a peptide reagent for ADC conjugation featuring a cleavable peptide sequence and a hydrophilic PEG spacer to enhance solubility in aqueous media.