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8256 results for "Bachem Americas"

8256 Results for: "Bachem Americas"

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Z-Val-Val-Arg-AMC

Supplier: Bachem Americas

Sequence: Z-Val-Val-Arg-AMC

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Boc-Leu-Arg-Arg-AMC · 2 HCl

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-Pro-Gly-OH

Supplier: Bachem Americas

250mg CAS: 2441-63-6 C9H15N3O4 FW: 229.24

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Fmoc-D-Ala-aldehyde

Supplier: Bachem Americas

Sequence: Fmoc-D-Ala-aldehyde

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Fmoc-Lys(Boc)-Thr(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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N-Fmoc-8-aminooctanoic acid

Supplier: Bachem Americas

Sequence: Fmoc-8-aminooctanoic acid

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Fmoc-7-Ahp-OH

Supplier: Bachem Americas

Sequence: Fmoc-7-aminoheptanoic acid

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(S)-2-(N-Fmoc-N-methyl-amino)-4-tritylsulfanyl-butyric acid

Supplier: Bachem Americas

Sequence: Fmoc-N-Me-Homocys(Trt)-OH

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Fmoc-β-(7-methoxy-coumarin-4-yl)-Ala-OH

Supplier: Bachem Americas

Sequence: Fmoc-β-(7-methoxy-coumarin-4-yl)-Ala-OH

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine hydrate

Supplier: Bachem Americas

Sequence: Fmoc-Ser-OH · H₂O

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N(α)-Cbz-L-histidine

Supplier: Bachem Americas

Sequence: Z-His-OH

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Z-Arg-AMC

Supplier: Bachem Americas

Sequence: Z-Arg-AMC

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H-Hyp-AMC

Supplier: Bachem Americas

Sequence: H-Hyp-AMC

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Z-Leu-Leu-OH

Supplier: Bachem Americas

Educt for the synthesis of proteasome inhibitors.

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H-Ala-Ala-Phe-AMC (free base)

Supplier: Bachem Americas

AAF-AMC, fluorogenic substrate for tripeptidyl peptidases I and II and for tripeptide aminopeptidase EC 3.4.11.4.

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MeOSuc-Ala-Ala-Pro-Met-AMC

Supplier: Bachem Americas

MeOSuc-AAPM-AMC, a fluorogenic substrate for cathepsin G.

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H-Lys-Ala-AMC

Supplier: Bachem Americas

KA-AMC, highly sensitive, fluorogenic substrate for dipeptidyl aminopeptidase II (DPP II) and Potent substrate for P. endodontalis dipeptidylpeptidase V (DPP 5).

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H-Lys-AMC

Supplier: Bachem Americas

Sequence: H-Lys-AMC

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L-Leucine(4-methyl-7-coumarinylamide)

Supplier: Bachem Americas

Sequence: H-Leu-AMC

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Suc-Ala-Phe-Lys-AMC Trifluoroacetate

Supplier: Bachem Americas

Suc-AFK-AMC, a highly sensitive fluorogenic substrate for plasmin. Suc-AFK-AMC was also used for assaying gingipain K.

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Suc-Ala-Ala-Phe-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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1-[4-(2-Hydroxyethyl)piperazin-1-yl]propan-2-ol

Supplier: Bachem Americas

Sequence: Z-Val-Ala-Asp-AMC
Synonym(s): Z-VAD-AMC

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Ac-Tyr-Val-Ala-Asp-AFC

Supplier: Bachem Americas

Sequence: Ac-Tyr-Val-Ala-Asp-AFC
Synonym(s): Ac-YVAD-AFC

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Ac-Tyr-Val-Ala-Asp-AMC

Supplier: Bachem Americas

Ac-YVAD-AMC is a fluorogenic substrate for caspase-1 (ICE). It displayed a Km of 8.5 ± 0.5 µM for recombinant human caspase-1.

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Z-Gly-Gly-OSu

Supplier: Bachem Americas

Sequence: Z-Gly-Gly-OSu

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Z-Gly-Gly-Gly-Gly-OH

Supplier: Bachem Americas

Sequence: Z-Gly-Gly-Gly-Gly-OH

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Z-Val-Ala-Asn-AMC

Supplier: Bachem Americas

Substrate for the determination of a new cysteine endopeptidase which is required for antigen processing. Z-VAN-AMC has been used as a fluorogenic substrate for porcine asparaginyl endopeptidase (AEP, legumain).

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tritylthio)butanoic acid

Supplier: Bachem Americas

Sequence: Fmoc-D-Homocys(Trt)-OH

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Z-Ala-OSu

Supplier: Bachem Americas

Sequence: Z-Ala-OSu

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Neuropeptide Y (22-36) Trifluoroacetate

Supplier: Bachem Americas

This C-terminal fragment of NPY is a more potent inhibitor of calmodulin-stimulated phosphodiesterase than NPY itself. The inhibitory effect obviously depends on the basic amphiphilic helical nature of the fragment.

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