Substance
ID:184495
Names and Identifiers
Synonyms
Acetyl-Ser-Asp-Lys-Pro
IUPAC Traditional name
1-{6-amino-2-[3-carboxy-2-(2-acetamido-3-hydroxypropanamido)propanamido]hexanoyl}pyrrolidine-2-carboxylic acid
IUPAC name
1-{6-amino-2-[3-carboxy-2-(2-acetamido-3-hydroxypropanamido)propanamido]hexanoyl}pyrrolidine-2-carboxylic acid
Properties
Safety Information
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature
-20°C
Product Information
Purity
≥97% (HPLC)
Pharmacology Properties
Gene Information
human ... GCG(2641)
Molecule Details
Amino Acid Sequence
Ac-Ser-Asp-Lys-Pro
Biochem/physiol Actions
Acetyl 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. It is a specific substrate for the N-terminal active site of angiotensin converting enzyme, which is responsible for its degradation in vivo.
Ac-Ser-Asp-Lys-Pro
Biochem/physiol Actions
Acetyl 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. It is a specific substrate for the N-terminal active site of angiotensin converting enzyme, which is responsible for its degradation in vivo.
Molecular Spectra
No Data Available
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References
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