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Catalog Number:
03740
CAS Number:
130597-31-8
Fmoc-(3S,4S-4-amino-3-hydroxy-5-cyclohexylpentanoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-ACHPA-OH
Documents
$127.79 /100MG
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Product Information

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the cyclohexyl group, enhances hydrophobic interactions, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability under various conditions, allowing for efficient coupling reactions and facilitating the synthesis of complex peptide sequences.

In addition to its role in peptide synthesis, this compound has shown potential in the development of therapeutic agents targeting various biological pathways. Its ability to form stable conjugates with other biomolecules opens avenues for innovative drug delivery systems and targeted therapies. With its favorable properties and practical applications, Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid stands out as an essential tool for researchers and industry professionals focused on advancing peptide-based therapeutics.

Synonyms
Fmoc-ACHPA-OH
CAS Number
130597-31-8
Purity
≥ 98% (HPLC)
Molecular Formula
C26H31NO5
Molecular Weight
437.5
MDL Number
MFCD00155626
PubChem ID
4712576
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-ACHPA-OH
CAS Number
130597-31-8
Purity
≥ 98% (HPLC)
Molecular Formula
C26H31NO5
Molecular Weight
437.5
MDL Number
MFCD00155626
PubChem ID
4712576
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, where its protective Fmoc group allows for selective deprotection and coupling.
  • Drug Development: Researchers leverage its unique structural properties to design and develop new pharmaceuticals, especially in the field of neuroactive compounds, enhancing the efficacy and specificity of drug candidates.
  • Bioconjugation: It is used in bioconjugation processes to attach peptides to various biomolecules, facilitating the creation of targeted therapies and diagnostic agents in biotechnology.
  • Material Science: The compound finds applications in the development of novel materials, particularly in creating hydrogels that mimic biological environments for tissue engineering applications.
  • Research on Amino Acid Analogues: It is valuable in studying amino acid analogues, helping researchers understand the structure-activity relationships that influence biological functions and interactions.

Citations