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You Searched For: (\u00B1)-Bromosuccinic+acid


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

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-4325.0005BA
Supplier: Bachem Americas
Image Unavailable-B-4310.0005BA

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

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-4310.0005BA
Supplier: Bachem Americas
Image Unavailable-B-4295.0005BA

Fmoc-Lys(Boc)-Ser(Psi(Me,Me)Pro)-Oh

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-4295.0005BA
Supplier: Bachem Americas
Image Unavailable-A-4210.0001BA

Boc-D-NptGly-OH

Description: Sequence: Boc-β-tBu-D-Ala-OH
Catalog Number: A-4210.0001BA
Supplier: Bachem Americas
Image Unavailable-F-1325.0005BA

2-Amino-4,4-dimethylpentanoic acid

Description: Sequence: H-β-tBu-DL-Ala-OH
Catalog Number: F-1325.0005BA
Supplier: Bachem Americas
Image Unavailable-A-3110.0005BA

Boc-β-t-butyl-L-alanine

Description: Sequence: Boc-β-tBu-Ala-OH
Catalog Number: A-3110.0005BA
Supplier: Bachem Americas
Image Unavailable-B-1150.0005BA

Fmoc-Leu-OPfp

Description: Sequence: Fmoc-Leu-OPfp
Catalog Number: B-1150.0005BA
Supplier: Bachem Americas
Image Unavailable-D-2350.0005BA

Fmoc-Leu 0.5-0.8 mmol/g on Wang resin 100-200 mesh

Description: Sequence: Fmoc-Leu-Wang resin (100-200 mesh)
Synonym(s): Fmoc-Leu-p-alkoxybenzyl alcohol resin
Catalog Number: D-2350.0005BA
Supplier: Bachem Americas
Image Unavailable-D-2535.0001BA

Fmoc-D-Leu 0.50 - 1.00 mmol/g on Wang resin 200-400 mesh

Description: Sequence: Fmoc-D-Leu-Wang resin (200-400 mesh)
Synonym(s): Fmoc-D-Leu-p-alkoxybenzyl alcohol resin
Catalog Number: D-2535.0001BA
Supplier: Bachem Americas
Image Unavailable-H-3018.0500BA

(N-Me-Tyr¹,N-Me-Arg⁷,D-Leu-NHEt⁸)-Dynorphin A (1-8) Trifluoroacetate

Description: The N-terminus of dynorphin, YGGFL, corresponds to Leu-enkephalin. So, dynorphin A (1-5) amide is filed as Leu-enkephalin amide (H-2745). For other opioid peptides see, the product families ‘Deltorphins and Dermorphins’, ‘Endorphins, MPF, Neoendorphins’, and ‘Opioid Peptides'.
Catalog Number: H-3018.0500BA
Supplier: Bachem Americas
Image Unavailable-CAAAJ64613-LB0

Z-Leu-Leu-Glu-7-amino-4-methylcoumarin

Description: A fluorogenic substrate for the peptidylglutamyl-peptide hydrolysing (caspase-like) activity of the proteasome which may be stimulated in the presence of Mg2+ ions and rapidly inactivated by N-acetylimidazole
Catalog Number: CAAAJ64613-LB0
Supplier: Thermo Scientific Chemicals

Certificates


Image Unavailable-B-3485.0005BA

Fmoc-L-leucinol

Description: Sequence: Fmoc-L-leucinol
Catalog Number: B-3485.0005BA
Supplier: Bachem Americas
Image Unavailable-CAAAJ64966-MCR

Z-Leu-Glu(OMe)-His-Asp(OMe)-Fluoromethyl Ketone Trifluoroacetate Salt Hydrate

Description: Molecular Formula: C32H43FN6O10.xC2HF3O2.yH2O
Formula Weight: 690.71(anhy)
Storage Temperature: -30°C to -10°C
Physical Form: Powder
Appearance: Off-white to pale brown
Solubility: Soluble in DMSO.
MDL No.: MFCD01862609
Catalog Number: CAAAJ64966-MCR
Supplier: Thermo Scientific Chemicals

Certificates


Image Unavailable-M-1535.0025BA

Leu-Leu

Description: Sequence: H-Leu-Leu-OH
Catalog Number: M-1535.0025BA
Supplier: Bachem Americas
Image Unavailable-E-2845.1000BA

H-His(3-Me)-OH

Description: Sequence: H-His(3-Me)-OH
Catalog Number: E-2845.1000BA
Supplier: Bachem Americas
Image Unavailable-E-3185.0250BA

N-Me-Lys(Z)-OH

Description: Sequence: N-Me-Lys(Z)-OH
Catalog Number: E-3185.0250BA
Supplier: Bachem Americas
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