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Catalog Number:
03953
CAS Number:
16 de septiembre de 2014
Boc -S -tritil-L-homocisteína
Purity:
≥ 95 % (HPLC)
Synonym(s):
Boc-L-HomoCys(Trt)-OH, (Ácido S -2-(Boc-amino)-4-tritilsulfanilbutírico
Documents
$86.23 /100 mg
Tamaño
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Product Information

Boc-S-trityl-L-homocysteine is a valuable compound in the field of peptide synthesis and medicinal chemistry. This derivative of homocysteine features a Boc (tert-butyloxycarbonyl) protecting group and a trityl group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing novel therapeutics. Its unique structure allows for selective reactions, facilitating the synthesis of complex peptides and proteins.

In pharmaceutical research, Boc-S-trityl-L-homocysteine is particularly useful in the development of inhibitors and modulators of biological pathways, especially those involving sulfur-containing amino acids. Its ability to serve as a building block in the synthesis of bioactive compounds positions it as a key player in drug discovery and development. Researchers can leverage its properties to create targeted therapies, making it an essential tool in both academic and industrial laboratories.

Synonyms
Boc-L-HomoCys(Trt)-OH, (Ácido S -2-(Boc-amino)-4-tritilsulfanilbutírico
CAS Number
16 de septiembre de 2014
Purity
≥ 95 % (HPLC)
Molecular Formula
C28H31NO4S
Molecular Weight
477.57
MDL Number
MFCD00672309
PubChem ID
19760053
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-HomoCys(Trt)-OH, (Ácido S -2-(Boc-amino)-4-tritilsulfanilbutírico
CAS Number
16 de septiembre de 2014
Purity
≥ 95 % (HPLC)
Molecular Formula
C28H31NO4S
Molecular Weight
477.57
MDL Number
MFCD00672309
PubChem ID
19760053
Appearance
Polvo blanco
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-S-trityl-L-homocysteine 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 therapeutics targeting various diseases.
  • Drug Development: It plays a crucial role in the design of new drugs, especially in the field of cancer research, where modifications of homocysteine can lead to novel anticancer agents.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Protein Engineering: It aids in the engineering of proteins with specific functionalities, making it valuable in biotechnology and enzyme design.
  • Analytical Chemistry: Boc-S-trityl-L-homocysteine is employed in various analytical techniques to study protein interactions and modifications, providing insights into biochemical pathways.

Citas