150828-96-9 Usage
Description
BOC-ORN(FMOC)-OH, also known as Nα-Fmoc-Nε-Boc-L-ornithine, is a synthetic amino acid building block that plays a crucial role in the field of peptide synthesis. It is a white to off-white powder with specific chemical properties that make it an essential component in the development of peptide-based drugs and therapies.
Uses
Used in Pharmaceutical Industry:
BOC-ORN(FMOC)-OH is used as a key building block for the synthesis of peptides, which are essential in the development of various pharmaceutical products. The growing peptide drug market demands fast and reliable synthesis methods, making BOC-ORN(FMOC)-OH a valuable asset in this industry.
Used in Research and Development:
In the field of research and development, BOC-ORN(FMOC)-OH is utilized for the synthesis of custom peptides and peptide-based compounds. This allows scientists to explore new therapeutic applications and develop innovative treatments for various diseases and conditions.
Used in Drug Delivery Systems:
BOC-ORN(FMOC)-OH can also be employed in the development of drug delivery systems, where it can be used to create peptide-based carriers for targeted drug delivery. This can improve the efficacy and bioavailability of drugs, as well as reduce potential side effects by ensuring that the drug is delivered directly to the intended site of action.
Overall, BOC-ORN(FMOC)-OH is a versatile and essential component in the pharmaceutical and biotechnology industries, playing a significant role in the synthesis of peptides and the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 150828-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150828-96:
(8*1)+(7*5)+(6*0)+(5*8)+(4*2)+(3*8)+(2*9)+(1*6)=139
139 % 10 = 9
So 150828-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H30N2O6/c1-25(2,3)33-24(31)27-21(22(28)29)13-8-14-26-23(30)32-15-20-18-11-6-4-9-16(18)17-10-5-7-12-19(17)20/h4-7,9-12,20-21H,8,13-15H2,1-3H3,(H,26,30)(H,27,31)(H,28,29)/t21-/m0/s1
150828-96-9Relevant articles and documents
Synthesis of Peptide–Adenine Conjugates as a New Tool for Monitoring Protease Activity
Masurier, Nicolas,Soualmia, Feryel,Sanchez, Pierre,Lefort, Valérie,Roué, Mia,Maillard, Ludovic T.,Subra, Gilles,Percot, Aline,El Amri, Chahrazade
, p. 176 - 183 (2019/01/04)
We took advantage of the powerful adenine SERS (Surface Enhanced Raman Spectroscopy) probe to design peptide–adenine conjugates as candidates for use as serine protease substrates. Whereas the direct introduction of the peptide sequence on the adenine exocyclic N6 amine gave an imidazopurinone derivative, the introduction of an aminoethyl linker between the adenine group and the peptide chain led to the expected candidate probes. These potential substrates were then evaluated for monitoring the hydrolytic activity of trypsin, used as a model protease, by HPLC and by SERS. We demonstrated that the Boc–VPR–adenine conjugate is a substrate of trypsin and constitutes a good starting point to design optimized substrates to monitor protease activity by SERS.
