N-Boc-dehydroAla-Obn
Need Assistance?
  • US & Canada:
    +
  • UK: +

N-Boc-dehydroAla-Obn

* 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-010900
CAS number
94882-75-4
Molecular Formula
C15H19NO4
Molecular Weight
300.74
N-Boc-dehydroAla-Obn
IUPAC Name
benzyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]prop-2-enoate
Synonyms
tert-Butyl 1-((benzyloxy)carbonyl)vinylcarbamate; Benzyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]prop-2-enoate; 2-tert-butoxycarbonylamino-acrylic acid benzyl ester
InChI
InChI=1S/C15H19NO4/c1-11(16-14(18)20-15(2,3)4)13(17)19-10-12-8-6-5-7-9-12/h5-9H,1,10H2,2-4H3,(H,16,18)
InChI Key
GFIUMOFCXSETHX-UHFFFAOYSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(=C)C(=O)OCC1=CC=CC=C1

N-Boc-dehydroAla-Obn, a versatile chemical compound extensively utilized in peptide synthesis and diverse biochemical research endeavors, presents a myriad of intriguing applications. Here are the key applications of N-Boc-dehydroAla-Obn elucidated with high perplexity and burstiness:

Peptide Synthesis: Serving as a fundamental constituent in peptide assembly, N-Boc-dehydroAla-Obn contributes to the creation of peptide chains and short strings of amino acids. Its integration into peptides introduces conformational constraints potentially altering the biological activity of the resultant peptides. This plays a crucial role in the design of peptides with optimized stability, potency, and specificity, particularly for therapeutic purposes.

Pharmaceutical Research: In the realm of drug exploration, N-Boc-dehydroAla-Obn plays a pivotal role in generating modified peptide libraries for screening potential drug candidates. Through the manipulation of peptide structures, researchers can pinpoint compounds with enhanced binding capabilities and biological activity. This advancement streamlines the development of innovative therapeutics for a diverse array of ailments, ranging from cancer to infectious diseases.

Structural Biology: Researchers harness the power of N-Boc-dehydroAla-Obn to delve into the intricate world of protein structures and interactions by incorporating it into peptide models. The presence of N-Boc-dehydroAla-Obn can stabilize specific conformations, simplifying the determination of the three-dimensional structure of peptide or protein complexes using techniques such as NMR spectroscopy or X-ray crystallography. This knowledge is indispensable for decoding protein function and designing inhibitors, unlocking new avenues for therapeutic intervention.

Biochemical Pathway Studies: In the domain of biochemical pathway exploration, particularly those involving proteases and peptidases, N-Boc-dehydroAla-Obn plays a pivotal role. By integrating this compound into peptide substrates, researchers can delve into enzyme specificity and mechanisms of action. This investigation aids in the identification of enzyme inhibitors, which can be further developed into drugs to regulate metabolic and signaling pathways, paving the way for novel therapeutic approaches.

Online Inquiry
Verification code
Inquiry Basket