N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine
Need Assistance?
  • US & Canada:
    +
  • UK: +

N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
CBZ-Amino Acids
Catalog number
BAT-004767
CAS number
1239425-84-3
Molecular Formula
C33H32N2O5
Molecular Weight
536.63
N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine
IUPAC Name
(2S)-2-[methyl(phenylmethoxycarbonyl)amino]-5-oxo-5-(tritylamino)pentanoic acid
Synonyms
Z-MeGln(Trt)-OH; N-Alpha-Carbobenzoxy-N-Alpha-Methyl-N-Omega-Trityl-L-Glutamine
Purity
95%
Storage
Store at 2-8°C
InChI
InChI=1S/C33H32N2O5/c1-35(32(39)40-24-25-14-6-2-7-15-25)29(31(37)38)22-23-30(36)34-33(26-16-8-3-9-17-26,27-18-10-4-11-19-27)28-20-12-5-13-21-28/h2-21,29H,22-24H2,1H3,(H,34,36)(H,37,38)/t29-/m0/s1
InChI Key
FLFOSUCMKHFXPM-LJAQVGFWSA-N
Canonical SMILES
CN(C(CCC(=O)NC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3)C(=O)O)C(=O)OCC4=CC=CC=C4

N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine is a synthetic derivative often used in peptide synthesis and biochemical studies. Here are some key applications of N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine:

Peptide Synthesis: This compound is widely applied in the synthesis of peptides as a protected amino acid building block. Its protective groups prevent unwanted reactions during the synthesis process, ensuring the correct assembly of peptide chains. This protection strategy is crucial for creating peptides with high purity and precise sequences.

Structural Biology: In structural biology, N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine serves as a tool for preparing peptide analogs used in protein interaction studies. By incorporating this compound into peptide structures, researchers can investigate binding affinities and conformational changes. These insights help elucidate protein-peptide interactions crucial for understanding biological processes.

Drug Design: The use of N-α-Carbobenzoxy-N-α-methyl-N-ω-trityl-L-glutamine in drug design involves creating peptide-based therapeutics with improved stability and bioavailability. By modifying specific amino acids, scientists can enhance the pharmacokinetic properties of peptide drugs.

Chemical Biology: In chemical biology, this compound is employed to probe and elucidate biological pathways involving glutamine residues. By introducing modified glutamine analogs into biological systems, researchers can study enzyme-substrate interactions and metabolic fluxes. These studies contribute to a deeper understanding of cellular processes and the development of novel biochemical tools.

Online Inquiry
Verification code
Inquiry Basket