Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
01992
Boc-S-4-methylbenzyl-D-cysteine 4-oxymethylphenylacetamidomethyl resin
Synonym(s):
Boc-D-Cys(pMeBzl)-PAM resin
Documents
$45.47 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-S-4-methylbenzyl-D-cysteine 4-oxymethylphenylacetamidomethyl is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Boc (tert-butyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its structure allows for enhanced stability and reactivity, making it an ideal choice for researchers focused on developing novel therapeutic agents.

In pharmaceutical research, Boc-S-4-methylbenzyl-D-cysteine is particularly valuable in the design of cysteine-containing peptides, which have shown promise in various biological applications, including enzyme inhibition and receptor modulation. Its ability to facilitate the incorporation of specific functional groups enhances the potential for creating targeted drug delivery systems. Additionally, the compound's unique properties can lead to improved solubility and bioavailability in drug formulations, making it a preferred choice for researchers aiming to optimize therapeutic efficacy.

Synonyms
Boc-D-Cys(pMeBzl)-PAM resin
MDL Number
MFCD00801175
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
Conditions
Store at 0-8°C
%DVB
1% DVB
General Information
Synonyms
Boc-D-Cys(pMeBzl)-PAM resin
MDL Number
MFCD00801175
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
Conditions
Store at 0-8°C
%DVB
1% DVB
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-S-4-methylbenzyl-D-cysteine 4-oxymethylphenylacetamidomethyl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial in developing complex peptide-based drugs.
  • Drug Development: Its unique structure can be used to create novel pharmaceutical compounds, particularly in designing targeted therapies for diseases such as cancer, where precision is key.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, linking biomolecules to enhance drug delivery systems or create targeted imaging agents, improving the efficacy of treatments.
  • Research in Neuroscience: It can be used to study neuroprotective effects and the role of specific amino acids in neurological disorders, providing insights that can lead to new therapeutic strategies.
  • Cosmetic Formulations: The compound's properties make it suitable for use in cosmetic products aimed at skin repair and rejuvenation, appealing to the growing market for effective skincare solutions.

Citations