Z-HomoArg-OH
Need Assistance?
  • US & Canada:
    +
  • UK: +

Z-HomoArg-OH

* 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-000877
CAS number
1313054-55-5
Molecular Formula
C15H22N4O4
Molecular Weight
322.36
IUPAC Name
(2S)-6-(diaminomethylideneamino)-2-(phenylmethoxycarbonylamino)hexanoic acid
Synonyms
(S)-2-(((Benzyloxy)carbonyl)amino)-6-guanidinohexanoic acid; Cbz-HomoArg-OH; Z-HoArg-OH
Storage
Store at 2-8 °C
InChI
InChI=1S/C15H22N4O4/c16-14(17)18-9-5-4-8-12(13(20)21)19-15(22)23-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2,(H,19,22)(H,20,21)(H4,16,17,18)/t12-/m0/s1
InChI Key
KTPKIMJAZDFELN-LBPRGKRZSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CCCCN=C(N)N)C(=O)O

Z-HomoArg-OH, a versatile chemical compound with diverse applications in the biochemical and biomedical fields, is harnessed in various ways. Here are the key applications presented with high perplexity and burstiness:

Enzyme Inhibition Studies: Serving as a cornerstone in the realm of enzyme kinetics research, Z-HomoArg-OH emerges as a potent inhibitor, facilitating detailed analyses of enzyme functions within intricate metabolic pathways. By selectively inhibiting enzymes, researchers unveil profound insights into potential drug targets for combating a myriad of metabolic disorders and other maladies.

Peptide Chemistry: Positioned at the forefront of peptide and protein synthesis, Z-HomoArg-OH assumes a crucial role as a versatile building block and protective agent. Leveraging its unique chemical properties, researchers sculpt peptides with customized sequences and functionalities, critical for the development of synthetic peptides utilized across diverse domains such as research, therapeutics, and diagnostics.

Drug Design and Development: Spearheading the frontier of drug discovery, Z-HomoArg-OH contributes significantly to the genesis of groundbreaking drug candidates with heightened therapeutic efficacy. Its integration into drug molecules enhances binding affinities and specificities towards biological targets, thereby fortifying the efficacy and safety profiles of potential therapeutic agents.

Structural Biology: Within the intricate realm of structural biology, Z-HomoArg-OH emerges as a pivotal component in unraveling the complex interactions between proteins and ligands. By binding to target proteins, it assists in elucidating the three-dimensional structures and binding sites of enzymes and receptors. This treasure trove of information underpins rational drug design and fosters a deep understanding of the molecular mechanisms of action.

Online Inquiry
Verification code
Inquiry Basket