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Catalog Number:
07059
CAS Number:
214852-52-5
Fmoc-Nω-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-homoarginine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-HomoArg(Pmc)-OH
Documents
$161.64 /100MG
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Product Information

Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-homoarginine is a specialized amino acid derivative that combines the benefits of Fmoc protection with a unique sulfonyl group, enhancing its utility in peptide synthesis and drug development. This compound is particularly valuable in the field of medicinal chemistry, where it serves as a building block for the synthesis of complex peptides and proteins. Its distinctive structure allows for improved solubility and stability, making it an excellent choice for researchers focused on developing novel therapeutics.

In addition to its role in peptide synthesis, this compound has shown potential in various applications, including targeted drug delivery and the development of enzyme inhibitors. The incorporation of the pentamethylchroman moiety enhances the compound's bioactivity, providing researchers with a versatile tool for exploring new biochemical pathways. With its unique properties, Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-homoarginine stands out as a promising candidate for advancing research in peptide-based therapies and bioconjugation strategies.

Synonyms
Fmoc-L-HomoArg(Pmc)-OH
CAS Number
214852-52-5
Purity
≥ 99% (HPLC)
Molecular Formula
C36H44N4O7S
Molecular Weight
676.8
MDL Number
MFCD00672707
PubChem ID
72964353
Appearance
White powder
Conditions
Store at RT
General Information
Synonyms
Fmoc-L-HomoArg(Pmc)-OH
CAS Number
214852-52-5
Purity
≥ 99% (HPLC)
Molecular Formula
C36H44N4O7S
Molecular Weight
676.8
MDL Number
MFCD00672707
PubChem ID
72964353
Appearance
White powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-homoarginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in targeting specific receptors in therapeutic applications, enhancing the efficacy of treatments.
  • Bioconjugation: The sulfonyl group facilitates bioconjugation processes, making it valuable in creating targeted drug delivery systems and improving the specificity of therapeutic agents.
  • Research in Neuroscience: This compound is used in studies related to neuropeptides, helping researchers understand their roles in neurological disorders and potential treatments.
  • Biomaterials: It can be incorporated into biomaterials for tissue engineering applications, promoting cell adhesion and growth due to its biocompatibility and functional properties.

Citations