5596 Results for: "Z-Asp-2,6-dichlorobenzoyloxymethylketon"
Corrected to: Z-Asp-2,6-dichlorobenzoyloxymethylketone
Z-Asp-2,6-dichlorobenzoyloxymethylketone
Supplier: Bachem Americas
Sequence: Z-Asp-2,6-dichlorobenzoyloxymethylketone
Synonym(s): Z-Asp-CH₂-DCB
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Z-Asp-2,6-dichlorobenzoyloxymethylketone ≥98% (by TLC)
Supplier: Enzo Life Sciences
Caspase inhibitor
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H-Asp(Leu-OH)-OH, Bachem
Supplier: Bachem Americas
See also G-4750 and β-aspartame (G-3725).
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Ac-Nle-Pro-Nle-Asp-AMC
Supplier: Bachem Americas
Substrates for measuring the chymotryptic, PGPH, and tryptic acitivity of the 20S or 26S proteasome. See also the thrombin substrate I-1140.
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H-Gly-Arg-Gly-Asp-Ser-Pro-Cys-OH Trifluoroacetate
Supplier: Bachem Americas
The integrin-binding heptapeptideGRGDSPC can be easily linked to carriers or surfaces.
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Ac-Gly-Asp-Tyr-Ser-His-Cys-Ser-Pro-Leu-Arg-Tyr-Tyr-Pro-Trp-Trp-Lys-Cys-Thr-Tyr-Pro-Asp-Pro-Glu-Gly-Gly-Gly-NH₂ Trifluoroacetate
Supplier: Bachem Americas
See also E-2410, Suc-Pro-OH, the product familiy 'Antihypertensive Peptides' and the subfamily 'Bradykinin-Potentiating Peptides (BPP)'.
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Fmoc-Asp(Otbu)-Ser(Psi(Me,Me)Pro)-Oh
Supplier: Bachem Americas
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.
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Cyclo(-Phe-Pro)
Supplier: Bachem Americas
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.
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Fmoc-D-Asp(OPp)-OH
Supplier: Bachem Americas
Sequence: Fmoc-D-Asp(2-phenylisopropyl ester)-OH
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L(+)-Aspartic acid ≥98%, powder, high purity
Supplier: VWR
Non-animal origin. White powder
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Fmoc-Asp(OtBu)-OPfp
Supplier: Bachem Americas
Sequence: Fmoc-Asp(OtBu)-OPfp
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Z-D-Asp(OtBu)-OH hydrate
Supplier: Bachem Americas
Sequence: Z-D-Asp(OtBu)-OH
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Fmoc-Asp(OtBu) 0.50-0.80 mmol/g on Wang resin 200-400 mesh
Supplier: Bachem Americas
Sequence: Fmoc-Asp(OtBu)-Wang resin (200-400 mesh)
Synonym(s): Fmoc-Asp(OtBu)-p-alkoxybenzyl alcohol resin
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Fmoc-D-Asp(OBzl)-OH
Supplier: Bachem Americas
Sequence: Fmoc-D-Asp(OBzl)-OH
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Supplier: Kimberly-Clark
$55.13 to $522.67
Supplier: Kimberly-Clark
$33.99 to $322.20
Supplier: Thermo Fisher Scientific
$170.20