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Click Chemistry

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    Results for Click Chemistry ( 905 )

      • 7-Bromoheptanoic acid

        Ref: BP-31149
        Sizes: 10 G, 5 G

        0

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      • Boc-PEG6-Val-Cit-PAB-OH

        Ref: BP-23217
        Sizes: 100 MG, 50 MG, 500 MG, 250 MG

        0

        Product detail

      • PC DBCO-PEG4-NHS ester

        Ref: BP-23308
        Sizes: 25 MG, 100 MG, 10 MG

        0

        Product detail

      • 4-azidobutyric acid

        Ref: BP-23875
        Sizes: 1 G, 500 MG, 250 MG

        0

        Product detail

      • 6-AZIDOHEXAN-1-AMINE

        Ref: BP-23965
        Sizes: 1 G, 500 MG, 5 G

        0

        Product detail

      • N-Acetyl-Calicheamicin

        Ref: BP-28001
        Sizes: 1 MG, 5 MG, 10 MG

        N-Acetyl-Calicheamicin is a potent enediyne antitumor antibiotic. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

        Product detail

      • FR901464

        Ref: BP-28003
        Sizes: 1 MG, 5 MG, 25 MG, 10 MG

        FR901464 is a potent anticancer moecule that lowers the mRNA levels of oncogenes and tumor suppressor genes. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • MC-Val-Ala-OH

        Ref: BP-28417
        Sizes: 1 G, 100 MG, 500 MG, 250 MG

        MC-Val-Ala-OH is an ADC linker featuring a maleimide, and a Val-Ala dipeptide. Maleimide is a thiol-specific covalent ligand which is most often used to label cysteine residues on target proteins, while Val-Ala is a protease-cleavable dipeptide. The C-terminal alanine is free to react with amines to form amides with a target molecule.

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      • Fmoc-Phe-Lys(Boc)-PAB

        Ref: BP-28419
        Sizes: 100 MG, 500 MG, 250 MG

        Fmoc-Phe-Lys(Boc)-PAB is a Phe-Lys dipeptide featuring an Fmoc-protected N-terminal, a Boc-protected ε-amine on the lysine, and a p-aminobenzyl (PAB) group. The benzylic alcohol on the PAB can be used to attach with reactive groups such as PNP for conjugation with drug payloads. The Fmoc protecting group may be removed by piperidine to allow the N-terminal to couple with carboxylic acids, while the Boc protecting group may be removed by acid towards the same ends. The Phe-Lys dipeptide may be cleaved by proteases to release a given drug payload via an elimination mechanism within the PAB group.

        Product detail