Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
04956
CAS Number:
109579-23-9
Ácido Boc-(3 S ,4 S -4-amino-3-hidroxi-5-(3-indolil)pentanoico
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-AHIPA( 3S ,4S - OH)
Documents
$141.41 /25 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(3S,4S)-4-amino-3-hydroxy-5-(3-indolyl)pentanoic acid is a versatile compound widely utilized in pharmaceutical research and peptide synthesis. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and facilitates its incorporation into various peptide sequences. Its unique structure, characterized by the presence of an indole group, makes it particularly valuable in the development of bioactive peptides and compounds with potential therapeutic applications, such as in cancer research and neurobiology.

Researchers appreciate this compound for its ability to serve as a building block in the synthesis of complex peptides, allowing for the exploration of new drug candidates. Its properties enable the modulation of biological activity, making it an essential tool in medicinal chemistry. The compound's stability and ease of handling further enhance its appeal, providing a reliable option for professionals seeking to innovate in drug development and biochemical research.

Synonyms
Boc-AHIPA( 3S ,4S - OH)
CAS Number
109579-23-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C18H24N2O5
Molecular Weight
348.39
MDL Number
MFCD00800346
PubChem ID
4712500
Appearance
Polvo blanco
Optical Rotation
[α] D 20 = -38 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-AHIPA( 3S ,4S - OH)
CAS Number
109579-23-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C18H24N2O5
Molecular Weight
348.39
MDL Number
MFCD00800346
PubChem ID
4712500
Appearance
Polvo blanco
Optical Rotation
[α] D 20 = -38 ± 2º (C=1 en MeOH)
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-(3S,4S)-4-amino-3-hydroxy-5-(3-indolyl)pentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly those with therapeutic potential, enhancing the development of new drugs.
  • Neuroscience Research: Its structural similarity to neurotransmitters makes it useful in studying neurological pathways and developing treatments for neurological disorders.
  • Drug Development: The compound's unique properties allow researchers to explore its efficacy in creating novel pharmaceuticals, particularly in oncology and neuropharmacology.
  • Bioconjugation: It can be utilized in bioconjugation processes, linking biomolecules for targeted drug delivery systems, improving therapeutic outcomes.
  • Analytical Chemistry: The compound is also employed in analytical methods to study protein interactions and enzyme activities, providing insights into biochemical processes.

Citas