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You Searched For: Boc-N-Me-Lys(Z)-OH+\u00B7+DCHA


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Fmoc-α-methylalanine

Supplier: Bachem Americas
Description: Sequence: Fmoc-Aib-OH
Synonym(s): Fmoc-α-Me-Ala-OH

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N-Methyl-D-aspartic acid

Supplier: Bachem Americas
Description: Sequence: N-Me-D-Asp-OH

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N-Methyl-L-serine

Supplier: Bachem Americas
Description: Sequence: N-Me-Ser-OH

Image Unavailable-E-2125.0005BA

N-Methyl-L-alanine

Supplier: Bachem Americas
Description: Sequence: N-Me-Ala-OH

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N-Methyl-L-tyrosine

Supplier: Bachem Americas
Description: Sequence: N-Me-Tyr-OH

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(S)-2-(Methylamino)succinic acid

Catalog Number: (E-2745.0250BA)
Supplier: Bachem Americas
Description: Sequence: N-Me-Asp-OH
Image Unavailable-B-3965.0001BA

Boc-Thr(Ile-Fmoc)-OH

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.

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Boc-Thr(Leu-Fmoc)-OH

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.

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Boc-Ala-D-Glu-NH₂

Catalog Number: (A-1165.0250BA)
Supplier: Bachem Americas
Description: Partially protected Ala-D-IsoGln and Ala-IsoGln dipeptides.
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Boc-Thr(Gly-Fmoc)-OH

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.

Image Unavailable-B-3980.0001BA

Boc-Ser(Val-Fmoc)-OH

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.

Image Unavailable-A-2690.0250BA

Boc-Met-Leu-Phe-OH

Catalog Number: (A-2690.0250BA)
Supplier: Bachem Americas
Description: Chemotactic peptide antagonist.
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1-Boc-DL-nipecotic acid ethyl ester ≥98.0% (by GC)

Supplier: TCI America
Description: CAS Number: 130250-54-3
MDL Number: MFCD04116274
Molecular Formula: C13H23NO4
Molecular Weight: 257.33
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 93
Melting point (°C): 37

SDS

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-M-1325.0050BA

Ac-Lys(Ac)-D-Ala-D-Ala-OH

Supplier: Bachem Americas
Description: See also F-3260.

Image Unavailable-H-1156.0025BA

Ac-Ser-Asp-Lys-Pro-OH

Supplier: Bachem Americas
Description: The bioactive tetrapeptide goralatide which corresponds to the N-terminus of Thymosin β₄, is a physiological regulator of hematopoiesis and inhibits the entry into the S-phase of murine and human hematopoietic stem cells. Ac-SDKP has been shown to reduce the damage to specific compartments in the bone marrow resulting from treatment with chemotherapeutic agents, ionizing radiations, hyperthermy, or phototherapy. It protects from doxorubicin-induced toxicity. Ac-SDKP is a physiological substrate of angiotensin I- converting enzyme (ACE).

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