Sfllrnpndkyepf

Base Information

• Chemical Name: Sfllrnpndkyepf
• CAS No.: 137339-65-2
• Molecular Formula: C₈₁H₁₁₈N₂₀O₂₃
• Molecular Weight: 1739.95
• ChEMBL ID: CHEMBL3184672
• Mol file: 137339-65-2.mol

Synonyms:Res (42-55);Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe;SFLL;SFLLRNPNDKYEPF;thrombin receptor agonist peptide (42-55);thrombin receptor peptide (42-55);thrombin receptor-derived polypeptide (42-55);TRAP-14 peptide;TRP (42-55)

Chemical Property of Sfllrnpndkyepf

Chemical Property:

• PSA: 713.20000
• LogP: 2.88170
• Storage Temp.: −20°C
• XLogP3: -7.4
• Hydrogen Bond Donor Count: 23
• Hydrogen Bond Acceptor Count: 26
• Rotatable Bond Count: 54
• Exact Mass: 1738.86787009
• Heavy Atom Count: 124
• Complexity: 3670

Purity/Quality:

98%Min ^*data from raw suppliers

Thrombin Receptor Agonist Peptide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 61
• Safety Statements: 53-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(C)CC(C(=O)NC(CC(C)C)C(=O)NC(CCCNC(=N)N)C(=O)NC(CC(=O)N)C(=O)N1CCCC1C(=O)NC(CC(=O)N)C(=O)NC(CC(=O)O)C(=O)NC(CCCCN)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)NC(CCC(=O)O)C(=O)N3CCCC3C(=O)NC(CC4=CC=CC=C4)C(=O)O)NC(=O)C(CC5=CC=CC=C5)NC(=O)C(CO)N
• Isomeric SMILES: CC(C)C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(=O)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N3CCC[C@H]3C(=O)N[C@@H](CC4=CC=CC=C4)C(=O)O)NC(=O)[C@H](CC5=CC=CC=C5)NC(=O)[C@H](CO)N

Technology Process of Sfllrnpndkyepf

There total 1 articles about Sfllrnpndkyepf 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:

1-(tert-butoxycarbonyl)-L-proline (15761-39-4,59433-50-0) + N-tert-butoxycarbonyl-L-phenylalanine (13734-34-4) + Boc-Asp(O-cyclohexyl)-OH (73821-95-1) + N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester (73821-97-3,133464-27-4) → Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe-OH (137339-65-2)

Guidance literature:

Multistep reaction;

DOI:10.1021/jm00020a029

upstream raw materials:

1-(tert-butoxycarbonyl)-L-proline

N-tert-butoxycarbonyl-L-phenylalanine

Boc-Asp(O-cyclohexyl)-OH

N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester

Refernces