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You Searched For: Fmoc-L-Thr+(Gal+\u03B2(1-3)GalNAc)-OH,+peracetate


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Fmoc-Thr(tBu)-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3915.0005BA)
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-3535.0005BA

Fmoc-Ala-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3535.0005BA)
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-3470.0005BA

Fmoc-Val-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3470.0005BA)
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-3440.0005BA

Fmoc-Ile-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3440.0005BA)
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-TCF0505-25G

N-(9-Fluorenylmethoxycarbonyl)-O-tert-butyl-L-threonine ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 71989-35-0
Molecular Formula: C23H27NO5
Molecular Weight: 397.47
Purity/Analysis Method: >98.0% (T,HPLC)
Form: Crystal
Melting point (°C): 133
Specific rotation [a]20/D: 15 deg (C=1, EtOAc)

SDS

Image Unavailable-TCF0608-1G

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-threonine ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 157355-81-2
Molecular Formula: C19H19NO5
Molecular Weight: 341.36
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: 15 deg (C=1, DMF)

SDS Certificates

Image Unavailable-B-3930.0005BA

Fmoc-Lys(Boc)-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3930.0005BA)
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.
Product Image-76660-802

N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-allyl-L-threonine 98%

Catalog Number: (76660-802)
Supplier: Ambeed
Description: N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-allyl-L-threonine, Purity: 98%, CAS Number: 1945973-89-6, Appearance: Solid, Storage: Sealed in dry, 2-8C, Size: 250MG
Image Unavailable-B-4310.0005BA

Fmoc-Thr(Tbu)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4310.0005BA)
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.
Product Image-76012-440

Anti-GAL3ST4 Rabbit Polyclonal Antibody

Catalog Number: (76012-440)
Supplier: Prosci
Description: This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate to the C-3' position of galactose residues in O-linked glycoproteins. This enzyme is highly specific for core 1 structures, with asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc being good substrates.
Image Unavailable-77437-942

Anti-GAL3ST4 Rabbit Polyclonal Antibody

Catalog Number: (77437-942)
Supplier: Bioss
Description: Catalyzes the transfer of sulfate to beta-1,3-linked galactose residues in O-linked glycoproteins. Good substrates include asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc.
Image Unavailable-B-4320.0005BA

Fmoc-Trp(Boc)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4320.0005BA)
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-4300.0005BA

Fmoc-Phe-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4300.0005BA)
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.
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-4325.0005BA

Fmoc-Tyr(Tbu)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4325.0005BA)
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.
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
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