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


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Catalog Number: (77622-710)
Supplier: Ambeed
Description: Fmoc-Phe-Thr(psi(Me,Me)pro)-OH

New Product


Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 042480-1G , MDL Number: MFCD00235882

Supplier: Bachem Americas
Description: Bachem also offers phosphothreonine derivatives.

Catalog Number: (TCG0344-5MG)
Supplier: TCI America
Description: CAS Number: 59837-15-9
Molecular Formula: C20H28N2O13
Molecular Weight: 504.45
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Storage Temperature: <0°C

SDS


Supplier: Ambeed
Description: N-(9-Fluorenylmethoxycarbonyl)-O-tert-butyl-L-threonine 97%

New Product

Supplier: Ambeed
Description: (2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(((benzyloxy)(hydroxy)phosphoryl)oxy)butanoic acid, Purity: 97%, CAS number: 175291-56-2, Appearance: Form: powder Colour: white to off white, Storage: Inert atmosphere, 2-8C, Size: 100MG

Catalog Number: (TS265330010)
Supplier: Thermo Scientific Chemicals
Description: N-(9-Fluorenylmethoxycarbonyl)-O-tert-butyl-L-threonine 98%

New Product


Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Catalog Number: (77622-712)
Supplier: Ambeed
Description: (4S,5R)-3-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid ≥95%

New Product


Catalog Number: (B-3985.0001BA)
Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.


Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Catalog Number: (102541-544)
Supplier: Matrix Scientific
Description: MF=C23H27NO5 MW=397.48 CAS=71989-35-0 MDL=MFCD00077075 100G


Supplier: Ambeed
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-threonine 97%

Catalog Number: (B-4085.0005BA)
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.


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.


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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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