Beefy meaty peptide

Base Information

• Chemical Name: Beefy meaty peptide
• CAS No.: 73984-05-1
• Molecular Formula: C₃₄H₅₇N₉O₁₆
• Molecular Weight: 847.877
• UNII: HE0DS1PZ2R
• DSSTox Substance ID: DTXSID601027510
• Nikkaji Number: J680.768B
• Wikipedia: Beefy_meaty_peptide
• Wikidata: Q4879783
• Mol file: 73984-05-1.mol

Synonyms:delicious peptide;Lys-Gly-Asp-Glu-Glu-Ser-Leu-Ala;lysyl-glycyl-aspartyl-glutamyl-glutamyl-seryl-leucyl-alanine

Chemical Property of Beefy meaty peptide

Chemical Property:

• Boiling Point: 1433.9±65.0 °C(Predicted)
• PKA: 3.42±0.10(Predicted)
• PSA: 425.17000
• Density: 1.372±0.06 g/cm3(Predicted)
• LogP: -1.04820
• Storage Temp.: -15°C
• XLogP3: -9.3
• Hydrogen Bond Donor Count: 14
• Hydrogen Bond Acceptor Count: 18
• Rotatable Bond Count: 30
• Exact Mass: 847.39232676
• Heavy Atom Count: 59
• Complexity: 1510

Purity/Quality:

98%Min ^*data from raw suppliers

Delicious Peptide (bovine) trifluoroacetate salt H-Lys-Gly-Asp-Glu-Glu-Ser-Leu-Ala-OH trifluoroacetate salt ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)CC(C(=O)NC(C)C(=O)O)NC(=O)C(CO)NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CC(=O)O)NC(=O)CNC(=O)C(CCCCN)N
• Isomeric SMILES: C[C@@H](C(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)CNC(=O)[C@H](CCCCN)N

Technology Process of Beefy meaty peptide

There total 3 articles about Beefy meaty peptide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.3%

α,ε-Dicarbobenzoxy-L-lysyl-glycyl-β-benzyl-L-aspartyl-γ-benzyl-L-glutamyl-γ-benzyl-L-glutamyl-O-benzyl-L-seryl-L-leucyl-L-alanine benzyl ester → H-L-Lys-Gly-L-Asp-L-Glu-L-Glu-L-Ser-L-Leu-L-Ala-OH (73984-05-1)

Guidance literature:

With hydrogen; palladium on activated charcoal; In methanol; for 5h;

DOI:10.1271/bbb1961.44.93

Reference yield:

Z-L-Lys(Z)-Gly-L-Asp(OBzl)-L-Glu(OBzl)-L-Glu(OBzl)-L-Ser-L-Leu-L-Ala-OBzl → H-L-Lys-Gly-L-Asp-L-Glu-L-Glu-L-Ser-L-Leu-L-Ala-OH (73984-05-1)

Guidance literature:

With hydrogen; palladium; In methanol;

Reference yield:

BOC-glycine (4530-20-5) + BOC-L-aspartic acid 4-benzyl ester (7536-58-5,98482-77-0) + Boc-Glu(OBzl)-OH (13574-13-5) + BOC-O-benzyl-L-serine (23680-31-1) → H-L-Lys-Gly-L-Asp-L-Glu-L-Glu-L-Ser-L-Leu-L-Ala-OH (73984-05-1)

Guidance literature:

Multistep reaction;

upstream raw materials:

BOC-glycine

BOC-L-aspartic acid 4-benzyl ester

Boc-Glu(OBzl)-OH

BOC-O-benzyl-L-serine