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Acetyl-Ser-Asp-Lys-Pro

HCID 4409396
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Basic information

CAS
127103-11-1
Standard SMILES
CC(=O)NC(CO)C(=O)NC(CC(=O)O)C(=O)NC(CCCCN)C(=O)N1CCCC1C(=O)O
InChIKey
HJDRXEQUFWLOGJ-UHFFFAOYSA-N
Molecular formula
C20H33N5O9
Average molar mass
487.5 g/mol
Monoisotopic mass
487.22782765

Names & identifiers

Preferred name
Acetyl-Ser-Asp-Lys-Pro
IUPAC
1-[2-[[2-[(2-acetamido-3-hydroxypropanoyl)amino]-3-carboxypropanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylic acid
English name
Goralatide
Molecular formula
C20H33N5O9
Molecular weight
487.5

Names & synonyms

Acetyl-Ser-Asp-Lys-Pro127103-11-1DTXSID30402957RefChem:317007DTXCID103538121-[2-[[2-[(2-acetamido-3-hydroxypropanoyl)amino]-3-carboxypropanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylic acidGoralatide?MFCD00076849C20H33N5O9Acetyl-serinyl-aspartyl-lysinyl-prolineSCHEMBL30148825N-Acetylseryl-alpha-aspartyllysylproline
Show more names
AC-SDKPSERASPENIDEThymosin β4 (1-4)Acetyl-SDKPAC-SER-ASP-LYS-PROAC-SER-ASP-LYS-PRO-OHGORALATIDEAC-SDKP-DELTAThymosin beta4 (1-4)AC-SER-ASP-LYS-PRO-O
Acetyl-Ser-Asp-Lys-Pro, >=97% (HPLC)1-[2-[[2-[(2-acetamido-3-hydroxy-propanoyl)amino]-3-carboxy-propanoyl]amino]-6-amino-hexanoyl]pyrrolidine-2-carboxylic acid

Database identifiers

CAS
127103-11-1
PubChem CID
4409396
DTXSID
DTXSID30402957

Properties

Computed structural properties

XLogP
-5.4
Topological polar surface area
228 Ų
Hydrogen bond donors
7
Hydrogen bond acceptors
10
Rotatable bonds
14
Heavy atoms
34
Formal charge
0
Complexity
776

Physicochemical properties

Boiling point
992 · 992.0±65.0 °C(predicted)
Density
1.382 · 1.382±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)
storage temp.
20 °C · −20°C
solubility
Soluble in DMSO
form
Solid
pka
3.39 · 3.39±0.20(predicted)
color
White to off-white
Water Solubility
2 mg/ml · Soluble in water at 2mg/ml
Sequence
H-Gln-Lys-Leu-Val-Phe-Phe-Ala-OH
FDA UNII
41538 E9P · H041538E9P
WGK Germany
3 · 3

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

wgk
3

Chemistry & industry

Applications · 1 item

UsesN-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.

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