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H-Lys-Ala-AMC

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

Image Unavailable-I-1255.1000BA

H-Lys-AMC

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

Image Unavailable-I-1245.0250BA

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

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

Image Unavailable-I-1325.0050BA

Suc-Ala-Phe-Lys-AMC Trifluoroacetate

Supplier: Bachem Americas
Description: Suc-AFK-AMC, a highly sensitive fluorogenic substrate for plasmin. Suc-AFK-AMC was also used for assaying gingipain K.

Image Unavailable-I-1315.0050BA

Suc-Ala-Ala-Phe-AMC

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.

Image Unavailable-I-1710.0005BA

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

Catalog Number: (I-1710.0005BA)
Supplier: Bachem Americas
Description: Sequence: Z-Val-Ala-Asp-AMC
Synonym(s): Z-VAD-AMC
Image Unavailable-I-1705.0005BA

Ac-Tyr-Val-Ala-Asp-AFC

Catalog Number: (I-1705.0005BA)
Supplier: Bachem Americas
Description: Sequence: Ac-Tyr-Val-Ala-Asp-AFC
Synonym(s): Ac-YVAD-AFC
Image Unavailable-I-1630.0025BA

Ac-Tyr-Val-Ala-Asp-AMC

Supplier: Bachem Americas
Description: 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.

Image Unavailable-C-1710.0025BA

Z-Gly-Gly-OSu

Supplier: Bachem Americas
Description: Sequence: Z-Gly-Gly-OSu

Image Unavailable-C-1745.0001BA

Z-Gly-Gly-Gly-Gly-OH

Catalog Number: (C-1745.0001BA)
Supplier: Bachem Americas
Description: Sequence: Z-Gly-Gly-Gly-Gly-OH
Image Unavailable-I-1840.0050BA

Z-Val-Ala-Asn-AMC

Supplier: Bachem Americas
Description: 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).

Image Unavailable-B-3610.0005BA

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

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Homocys(Trt)-OH

Image Unavailable-C-1025.0025BA

Z-Ala-OSu

Supplier: Bachem Americas
Description: Sequence: Z-Ala-OSu

Image Unavailable-H-9305.0005BA

Neuropeptide Y (22-36) Trifluoroacetate

Catalog Number: (H-9305.0005BA)
Supplier: Bachem Americas
Description: 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.
Image Unavailable-B-4095.0005BA

Fmoc-Asn(Trt)-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-4095.0005BA)
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.
Image Unavailable-B-4105.0005BA

Fmoc-Gln(Trt)-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-4105.0005BA)
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.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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