Boc-D-Glu(OBzl)-OMe
Need Assistance?
  • US & Canada:
    +
  • UK: +

Boc-D-Glu(OBzl)-OMe

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

Category
BOC-Amino Acids
Catalog number
BAT-000939
CAS number
110473-10-4
Molecular Formula
C18H25NO6
Molecular Weight
351.40
IUPAC Name
5-O-benzyl 1-O-methyl (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanedioate
Synonyms
N-α-(t-Butoxycarbonyl)-D-glutamic acid γ-benzyl ester α-methyl ester; 5-O-benzyl 1-O-methyl (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanedioate
Storage
Store at 2-8 °C
InChI
InChI=1S/C18H25NO6/c1-18(2,3)25-17(22)19-14(16(21)23-4)10-11-15(20)24-12-13-8-6-5-7-9-13/h5-9,14H,10-12H2,1-4H3,(H,19,22)/t14-/m1/s1
InChI Key
KHCZTGSAKNZBOV-CQSZACIVSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CCC(=O)OCC1=CC=CC=C1)C(=O)OC

Boc-D-Glu(OBzl)-OMe, a chemical compound renowned for its role in peptide synthesis, offers unique advantages in diverse bioscience applications. Here are four key applications:

Peptide Synthesis: Widely embraced in the realm of peptide synthesis, Boc-D-Glu(OBzl)-OMe stands out as a go-to protected amino acid for crafting intricate peptide sequences. Its Boc (tert-butyloxycarbonyl) group functions as a transient shield for the amino moiety, safeguarding against unwanted reactions during peptide elongation. This protective measure enables precise coupling reactions, fostering the assembly of highly complex peptide structures.

Pharmaceutical Development: Within the domain of pharmaceutical research, Boc-D-Glu(OBzl)-OMe plays a pivotal role in the design and synthesis of peptide-based therapeutic agents. Peptides can be tailored to exhibit specific biological functions, and the compound assists in constructing these bioactive molecules. Its utilization guarantees the stability and efficacy of intermediate compounds throughout the drug development journey, propelling advancements in medicinal science.

Bioconjugation: Delving into the world of bioconjugation techniques, Boc-D-Glu(OBzl)-OMe emerges as a versatile tool for attaching peptides or proteins to other molecules for therapeutic or diagnostic purposes. The compound’s protected glutamic acid facilitates precise modifications, enabling the selective attachment of diverse functional groups. This flexibility is crucial for generating conjugates endowed with enhanced properties, like superior solubility and heightened target specificity, elevating the field of biomolecular interactions.

Proteomics Research: In the dynamic realm of proteomics, Boc-D-Glu(OBzl)-OMe plays a crucial role in unraveling the intricacies of protein structure and function by facilitating the synthesis of modified peptides. Researchers leverage this compound to delve into post-translational modifications or mimic protein interactions, shedding light on protein dynamics and molecular relationships. This application proves indispensable for advancing our understanding of cell biology and disease mechanisms, pushing the boundaries of scientific exploration.

Online Inquiry
Verification code
Inquiry Basket