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You Searched For: Fmoc-N-Me-D-Leu-OH


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Image Unavailable-B-4315.0005BA

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

Catalog Number: (B-4315.0005BA)
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-4270.0005BA

Fmoc-Ala-Ser(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4270.0005BA)
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-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.
Image Unavailable-B-4295.0005BA

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

Catalog Number: (B-4295.0005BA)
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-4305.0005BA

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

Catalog Number: (B-4305.0005BA)
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.
Image Unavailable-B-1150.0005BA

Fmoc-Leu-OPfp

Catalog Number: (B-1150.0005BA)
Supplier: Bachem Americas
Description: Sequence: Fmoc-Leu-OPfp
Image Unavailable-H-3018.0500BA

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

Catalog Number: (H-3018.0500BA)
Supplier: Bachem Americas
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'.
Image Unavailable-D-2350.0005BA

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

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

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

Catalog Number: (D-2535.0001BA)
Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Leu-Wang resin (200-400 mesh)
Synonym(s): Fmoc-D-Leu-p-alkoxybenzyl alcohol resin
Image Unavailable-CAAAJ64613-LB0

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

Catalog Number: (CAAAJ64613-LB0)
Supplier: Thermo Scientific Chemicals
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

Certificates


Image Unavailable-G-4275.0050BA

N-Me-Val-Leu-anilide

Supplier: Bachem Americas
Description: These N-modified peptides are used as standards for the determination of the extent of the N-terminal globin modification in erythrocytes of people exposed to alkylating agents or to triazinyl derivatives. Isolated globin is submitted to Edman degradation and the thiohydantoin derivatives are separated and quantified by GC-MS, with the help of these standards.

Image Unavailable-H-3266.1000BA

Human;Rat (D-Phe¹²,Nle²¹·³⁸,alpha-Me-Leu³⁷)-CRF (12-41) Trifluoroacetate

Supplier: Bachem Americas
Description: Potent and long-acting CRF antagonist.

Image Unavailable-CAAAJ64966-MCR

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

Catalog Number: (CAAAJ64966-MCR)
Supplier: Thermo Scientific Chemicals
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

Certificates


Image Unavailable-B-3485.0005BA

Fmoc-L-leucinol

Supplier: Bachem Americas
Description: Sequence: Fmoc-L-leucinol

Image Unavailable-M-1535.0025BA

Leu-Leu

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

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