8 Results for "

Boc-protected dipeptide

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "Boc-protected dipeptide" in MCE Product Catalog:

Cat. No.: HY-W039756
CAS No.: 27317-69-7
Synonyms: NSC 334362
Research Areas:  

Infection Others

Boc-Ala-Ala-OH (NSC 334362) is a Boc-protected dipeptide and molecular building block. Boc-Ala-Ala-OH binds to metallopeptide cage 12. Boc-Ala-Ala-OH serves as a precursor for Boc-Ala-Ala-Asp-SBzl and Boc-Ala-Ala-Asp-CH2Cl .
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Cat. No.: HY-P4716
CAS No.: 64905-10-8
Research Areas:  

Inflammation/Immunology

Boc-D-Trp(For)-OH, containing the amino acid tryptophan, is synthesized by the ammonolysis of Boc-protected D-alanine, followed by cyclization to form a dipeptide with ninhydrin. Boc-D-Trp(For)-OH has pharmacological properties, including inhibition of growth hormone release, induction of sleep and antiinflammatory .
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Cat. No.: HY-W800624
CAS No.: 2055024-55-8
Target:  

ADC Linkers

Research Areas:  

Cancer

Boc-PEG2-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. The benzylic alcohol on the PAB can be used to attach with reactive groups such as PNP for conjugation with drug payloads. The Boc protecting group may be removed with acid to reveal a primary amine which may be used in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell.
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Cat. No.: HY-W800625
CAS No.: 2055024-54-7
Target:  

ADC Linkers

Research Areas:  

Cancer

Boc-PEG4-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. The benzylic alcohol on the PAB can be used to attach with reactive groups such as PNP for conjugation with drug payloads. The Boc protecting group may be removed with acid to reveal a primary amine which may be used in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell.
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Cat. No.: HY-W800837
CAS No.: 2231240-82-5
Target:  

ADC Linkers

Research Areas:  

Cancer

t-Boc-N-amido-PEG4-Val-Cit is a protease-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit dipeptide. The Val-Cit dipeptide is cleavable by cell proteases and features a carboxylic acid which is free for coupling reactions with amines to form amides. The Boc can be removed under acidic conditions to reveal a free primary amine, which may be used in a variety of reactions such as coupling or reductive amination.
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Cat. No.: HY-W800621
CAS No.: 2055024-59-2
Target:  

ADC Linkers

Research Areas:  

Cancer

Fmoc-PEG2-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. 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 with piperidine to reveal a primary amine for use in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell.
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Cat. No.: HY-W800622
CAS No.: 2055024-58-1
Target:  

ADC Linkers

Research Areas:  

Cancer

Fmoc-PEG4-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. 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 with piperidine to reveal a primary amine which may be used in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell.
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Cat. No.: HY-W800623
CAS No.: 2055024-57-0
Target:  

ADC Linkers

Research Areas:  

Cancer

Fmoc-PEG6-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. 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 with piperidine to reveal a primary amine which may be used in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell.
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