You Searched For: Z-Asp-2,6-dichlorobenzoyloxymethylketone


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Catalog Number: (89146-632)
Supplier: Enzo Life Sciences
Description: Caspase inhibitor


Supplier: Bachem Americas
Description: Sequence: Z-Asp-2,6-dichlorobenzoyloxymethylketone
Synonym(s): Z-Asp-CH₂-DCB

Catalog Number: (G-1600.0250BA)
Supplier: Bachem Americas
Description: See also G-4750 and β-aspartame (G-3725).


Supplier: Bachem Americas
Description: Substrates for measuring the chymotryptic, PGPH, and tryptic acitivity of the 20S or 26S proteasome. See also the thrombin substrate I-1140.

Supplier: Bachem Americas
Description: The integrin-binding heptapeptideGRGDSPC can be easily linked to carriers or surfaces.

Supplier: Bachem Americas
Description: See also E-2410, Suc-Pro-OH, the product familiy 'Antihypertensive Peptides' and the subfamily 'Bradykinin-Potentiating Peptides (BPP)'.

Supplier: Bachem Americas
Description: Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Catalog Number: (B-4275.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Supplier: Bachem Americas
Description: Sequence: H-D-Asp-OtBu

Supplier: Bachem Americas
Description: Sequence: H-Asp-AMC

Supplier: Bachem Americas
Description: Sequence: H-Asp-βNA

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Asp-ODmb

Supplier: Bachem Americas
Description: Sequence: Ac-Asp-OMe

Supplier: Bachem Americas
Description: Sequence: Fmoc-Asp-allyl ester

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Asp(2-phenylisopropyl ester)-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-Asp-ODmb

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