You Searched For: 4-Chlorophenyl+methyl+sulfone


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Description: Sequence: Fmoc-α-Me-Leu-OH
Catalog Number: B-3665.0001BA
Supplier: Bachem Americas


Description: Sequence: Fmoc-α-Me-D-Leu-OH
Catalog Number: B-4080.0001BA
Supplier: Bachem Americas


Description: N-Fmoc-N-methyl-D-leucine, 97%
Catalog Number: AAH63895-06
Supplier: Thermo Scientific Chemicals

Description: Sequence: Fmoc-N-Me-Leu-OH
Catalog Number: B-2035.0005BA
Supplier: Bachem Americas


Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-leucine, Purity: >98.0%(HPLC)(T), CAS number: 103478-62-2, Molecular Formula: C22H25NO4, Molecular Weight: 367.45, Synonym: Fmoc-N-Me-Leu-OH, N-Fmoc-N-methyl-L-leucine, Size: 1G
Catalog Number: TCF1028-1G
Supplier: TCI America


Description: N-Fmoc-N-methyl-L-leucine, 98%
Catalog Number: AAH63453-06
Supplier: Thermo Scientific Chemicals

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-3540.0005BA
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-3545.0005BA
Supplier: Bachem Americas


Description: Sequence: H-α-Me-Leu-OH
Catalog Number: F-4090.0001BA
Supplier: Bachem Americas


Description: Sequence: Fmoc-His(1-Me)-OH
Catalog Number: B-3375.1000BA
Supplier: Bachem Americas


Description: Sequence: H-α-Me-D-Leu-OH
Catalog Number: F-4155.0005BA
Supplier: Bachem Americas


Description: Sequence: Z-N-Me-Leu-OH
Catalog Number: C-2240.0005BA
Supplier: Bachem Americas


Description: Sequence: H-α-Me-DL-Leu-OH
Catalog Number: F-1800.0025BA
Supplier: Bachem Americas


Description: Building block for oxytocin and vasopressin analogs as carbetocin, and for structure-activity studies.
Catalog Number: B-4255.0005BA
Supplier: Bachem Americas


Description: MeIle derivative used in the Fmoc-SPPS of cyclosporin and compstatin analogs.
Catalog Number: B-4215.0005BA
Supplier: Bachem Americas


Description: Sequence: Fmoc-Trp(Me)-OH
Catalog Number: B-3875.0005BA
Supplier: Bachem Americas


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