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Catalog Number:
12779
CAS Number:
229639-48-9
Boc-L-β-homotriptófano
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-β-HomoTrp-OH, Ácido ( S -3-(Boc-amino)-4-(3-indolil)butírico
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-L-b-homotryptophan is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical research. This compound is recognized for its unique structure, which includes a tert-butoxycarbonyl (Boc) protecting group that enhances its stability and usability in various chemical reactions. Its indole side chain contributes to its potential in designing bioactive peptides, making it a valuable building block in the development of novel therapeutics and research applications. Researchers utilize Boc-L-b-homotryptophan in the synthesis of peptides that can target specific biological pathways, offering promising avenues in drug discovery and development.

In addition to its applications in peptide synthesis, Boc-L-b-homotryptophan is also explored for its potential in the development of enzyme inhibitors and receptor ligands. Its ability to mimic natural amino acids while providing enhanced stability makes it an attractive option for medicinal chemists. The compound's unique properties allow for the creation of more effective and selective compounds, paving the way for advancements in targeted therapies. With its broad range of applications, Boc-L-b-homotryptophan stands out as a key player in the field of chemical research and pharmaceutical development.

Synonyms
Boc-L-β-HomoTrp-OH, Ácido ( S -3-(Boc-amino)-4-(3-indolil)butírico
CAS Number
229639-48-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C17H22N2O4
Molecular Weight
318.37
MDL Number
MFCD01862938
PubChem ID
3933942
Appearance
Sólido de color blanco a blanquecino
Optical Rotation
[a] D 25 = -22 ± 2 º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-β-HomoTrp-OH, Ácido ( S -3-(Boc-amino)-4-(3-indolil)butírico
CAS Number
229639-48-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C17H22N2O4
Molecular Weight
318.37
MDL Number
MFCD01862938
PubChem ID
3933942
Appearance
Sólido de color blanco a blanquecino
Optical Rotation
[a] D 25 = -22 ± 2 º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-b-homotryptophan is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of peptide-based drugs and therapeutics.
  • Drug Development: Its unique structure allows for the modification of bioactive compounds, making it valuable in the pharmaceutical industry for creating novel drug candidates.
  • Biochemical Research: Researchers employ this compound to study protein interactions and enzyme activities, aiding in the understanding of various biological processes.
  • Cosmetic Applications: The compound is explored in the formulation of skin care products due to its potential skin-repairing properties, appealing to the cosmetic industry.
  • Neuroscience Studies: Its structural similarity to neurotransmitters makes it a candidate for research in neuropharmacology, helping to investigate treatments for neurological disorders.

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