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Catalog Number:
07366
CAS Number:
204199-67-7
Boc-Leu- ψCH2NH )-Asp(OBzl)-OH
Purity:
≥ 99 % (HPLC)
Documents
$181.67 /100 mg
Taille
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Product Information

Boc-Leu-y(CH2NH)-Asp(OBzl)-OH is a specialized peptide derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and bioavailability, making it an ideal candidate for pharmaceutical applications. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, facilitating the synthesis of complex peptides and proteins. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound for the development of targeted therapies, particularly in oncology and neurology, where peptide-based drugs are gaining traction.

The compound's ability to incorporate into larger peptide chains while maintaining its functional integrity makes it invaluable for creating novel therapeutic agents. Its applications extend to the synthesis of peptide conjugates and the development of drug delivery systems, where its properties can be tailored for specific therapeutic outcomes. With its robust profile, Boc-Leu-y(CH2NH)-Asp(OBzl)-OH stands out as a versatile tool for researchers aiming to innovate in peptide-based therapeutics.

CAS Number
204199-67-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H34N2O6
Molecular Weight
422.52
MDL Number
MFCD00273438
PubChem ID
4712524
Appearance
Poudre blanche amorphe
Optical Rotation
[α] D = -25 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
CAS Number
204199-67-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H34N2O6
Molecular Weight
422.52
MDL Number
MFCD00273438
PubChem ID
4712524
Appearance
Poudre blanche amorphe
Optical Rotation
[α] D = -25 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-Leu-y(CH2NH)-Asp(OBzl)-OH 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 therapeutic agents. Its protective groups help in selective reactions, enhancing yield and purity.
  • Drug Development: Used in the design of novel drug candidates, it allows researchers to modify peptide structures for improved efficacy and reduced side effects, making it valuable in pharmaceutical research.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to create targeted drug delivery systems. This is particularly beneficial in cancer therapy where precision is crucial.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to the understanding of neurological pathways and potential treatments for neurodegenerative diseases.
  • Custom Synthesis: Its versatility allows for customization in various research applications, catering to specific needs in academic and industrial laboratories, thus facilitating innovative research approaches.

Citations