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N-Acetyl-Ser-Asp-Lys-Pro

Cat. No. Size Price Figures
RP10555-5 mg
5 mg
$ 23.75
HPLC:  20060721145617  (PDF)
MS:  20060721145557  (PDF)

STRUCTURE:
Ac-Ser-Asp-Lys-Pro Structure
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References:
  • Wdzieczak-Bakala J, et al. Catabolism of the tetrapeptide N-Ac-Ser-Asp-Lys-Pro (AcSDKP), an inhibitor of hematopoietic stem cell (CFU-S) proliferation, following in vitro incubation with hematopoietic tissues from normal and leukemic mice. Bull Cancer. May 1993; 80(5): 391-396.
  • Wang D, et al. N-acetyl-seryl-aspartyl-lysyl-proline stimulates angiogenesis in vitro and in vivo. Am. J. Physiol Heart Circ. Physiol. Nov 2004; 287(5): H2099-H2105.
  • Rioli V, et al. Novel natural peptide substrates for endopeptidase 24.15, neurolysin, and angiotensin-converting enzyme. J. Biol. Chem. Mar 2003; 278(10): 8547-8555.
Full Name
N-Acetyl-Ser-Asp-Lys-Pro
Alias AcSDKP; Ac-S-D-K-P
Sequence
(one-letter code)
SDKP
Sequence
(three-letter code)
{SER}{ASP}{LYS}{PRO}
DescriptionAcetyl Ser-Asp-Lys-Pro is formed in bone marrow cells by enzymatic processing of thymosin β4. It inhibits the entry of pluripotent hemopoietic stem cells into S-phase of the cell cycle and protects against Ara-C lethality in mice. Acetyl Ser-Asp-Lys-Pro is also a specific substrate for the N-terminal active site of angiotensin-converting enzyme, which is responsible for its degradation in vivo.
FormulaC20H33N5O9
M.W.487.5
Cas127103-11-1
Purity> 95%
StorageStore at -20°C.
N-TerminalAC
Notes(CFU-S = Spleen Colony-Forming Units) N-Acetyl-Ser-Asp-Lys-Pro exerts a high inhibitory activity on the proliferation of hematopoietic pluripotent stem cells
* For Non-Clinical Research Use Only *


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