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Catalog Number:
32553
CAS Number:
1926163-06-5
Fmoc-Leu-Cys(Psi(Dmp,H)pro)-OH
Purity:
≥ 98% (HPLC, TLC)
Synonym(s):
Fmoc-Leu-Cys(Y(Dmp,H)pro)-OH
Documents
$90.00 /100MG
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Product Information

Fmoc-Leu-Cys(Psi(Dmp,H)pro)-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry and biochemistry for its ability to facilitate the formation of complex peptides with enhanced stability and bioactivity. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during synthesis, making it an ideal choice for researchers looking to streamline their peptide assembly processes.

In practical applications, Fmoc-Leu-Cys(Psi(Dmp,H)pro)-OH is utilized in the development of peptide-based therapeutics, where precise control over amino acid sequences is essential for achieving desired biological activity. Its thiazolidine ring structure contributes to the compound's stability and potential for incorporation into various peptide frameworks, enhancing the efficacy of drug candidates. Researchers in pharmaceutical and biotechnology sectors will find this compound particularly beneficial for advancing their peptide synthesis projects and exploring novel therapeutic avenues.

Synonyms
Fmoc-Leu-Cys(Y(Dmp,H)pro)-OH
CAS Number
1926163-06-5
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C33H36N2O7S
Molecular Weight
604.72
MDL Number
MFCD28053687
PubChem ID
139035547
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
General Information
Synonyms
Fmoc-Leu-Cys(Y(Dmp,H)pro)-OH
CAS Number
1926163-06-5
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C33H36N2O7S
Molecular Weight
604.72
MDL Number
MFCD28053687
PubChem ID
139035547
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Leu-Cys(Psi(Dmp,H)pro)-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 cyclic peptides that have enhanced stability and bioactivity.
  • Drug Development: Its unique structure allows for the creation of novel therapeutic agents, especially in the fields of oncology and immunology, where targeted therapies are crucial.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of drugs to antibodies for targeted delivery, improving efficacy while reducing side effects.
  • Research in Protein Engineering: It plays a significant role in protein engineering, aiding in the design of proteins with specific functions, which is essential for advancements in biotechnology.
  • Diagnostics: The chemical is also applied in the development of diagnostic tools, particularly in assays that require high specificity and sensitivity, enhancing disease detection capabilities.

Citations