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Catalog Number:
32568
CAS Number:
1188402-17-6
Fmoc-Ala-(Dmb)Gly-OH
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-Ala- N -(2,4-diméthoxybenzyl)-Gly-OH
Documents
$88.63 /100 mg
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Product Information

Fmoc-Ala-(Dmb)Gly-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique structure that combines the protective Fmoc (fluorenylmethyloxycarbonyl) group with a dimethoxybenzyl (Dmb) moiety, making it an excellent choice for researchers focusing on solid-phase peptide synthesis. Its ability to provide stability and protection during the synthesis process enhances the efficiency of creating complex peptides, which are crucial in various therapeutic applications, including cancer treatment and vaccine development.

Moreover, Fmoc-Ala-(Dmb)Gly-OH is recognized for its compatibility with automated synthesizers, allowing for streamlined workflows in laboratories. Its distinctive properties facilitate the introduction of specific amino acid sequences, enabling the design of peptides with tailored biological activities. Researchers can leverage this compound to explore novel therapeutic avenues, making it an essential tool in the arsenal of peptide chemists and pharmaceutical developers.

Synonyms
Fmoc-Ala- N -(2,4-diméthoxybenzyl)-Gly-OH
CAS Number
1188402-17-6
Purity
≥ 95 % (HPLC)
Molecular Formula
C29H30N2O7
Molecular Weight
518.57
MDL Number
MFCD08064314
PubChem ID
138114563
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Fmoc-Ala- N -(2,4-diméthoxybenzyl)-Gly-OH
CAS Number
1188402-17-6
Purity
≥ 95 % (HPLC)
Molecular Formula
C29H30N2O7
Molecular Weight
518.57
MDL Number
MFCD08064314
PubChem ID
138114563
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-Ala-(Dmb)Gly-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 solid-phase peptide synthesis, allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, which are increasingly important in treating various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach peptides to other biomolecules, enhancing the efficacy of drugs and diagnostics.
  • Research in Protein Engineering: It aids in the modification of proteins to study structure-function relationships, providing insights that can lead to innovations in biotechnology.
  • Academic Research: This compound is a valuable tool in academic labs for studying peptide interactions and functions, contributing to advancements in molecular biology and biochemistry.

Citations