N-Acetyl-Ser-Asp-Lys-Pro

Catalog Number	Quantity
J66430.LB0 also known as J66430-#0	5 mg

Catalog number J66430.LB0

also known as J66430-#0

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Chemical Identifiers

CAS127103-11-1

IUPAC Name1-{6-amino-2-[3-carboxy-2-(2-acetamido-3-hydroxypropanamido)propanamido]hexanoyl}pyrrolidine-2-carboxylic acid

Molecular FormulaC20H33N5O9

InChI KeyHJDRXEQUFWLOGJ-UHFFFAOYNA-N

SMILESCC(=O)NC(CO)C(=O)NC(CC(O)=O)C(=O)NC(CCCCN)C(=O)N1CCCC1C(O)=O

Specifications

Appearance (Color)White

Purity≥94.0%

Molecular WeightConsistent (Theoretical: 487.5)

FormLyophilized Powder

N-Acetyl-Ser-Asp-Lys-Pro 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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
N-Acetyl-Ser-Asp-Lys-Pro 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

RUO – Research Use Only

General References:

C S Anthony; G Masuyer; E D Sturrock; K R Acharya. Structure based drug design of angiotensin-I converting enzyme inhibitors. Current Medicinal Chemistry.2012, 19, (6), 845-855.
A Rousseau-Plasse; J Wdzieczak-Bakala; M Lenfant; E Ezan, R Genet; S Robinson; T Briscoe; J Melville; A Riches. Lisinopril, an angiotensin I-converting enzyme inhibitor, prevents entry of murine hematopoietic stem cells into the cell cycle after irradiation in vivo. Experimental Hematology.1998, 26, (11), 1074-1079.

Contents & Storage

Store at -20°C