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Catalog Number:
05938
CAS Number:
97233-92-6
Nω-(4-Toluenesulfonyl)-D-arginine
Purity:
≥ 97% (HPLC)
Synonym(s):
D-Arg(Tos)-OH
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Product Information

Nw-(4-Toluenesulfonyl)-D-arginine is a specialized amino acid derivative that plays a significant role in biochemical research and pharmaceutical applications. This compound, recognized for its unique sulfonyl group, is particularly valuable in the synthesis of peptide-based drugs and as a building block in the development of protease inhibitors. Its structural characteristics enhance its ability to interact with biological targets, making it a crucial component in drug discovery and development processes.

Researchers utilize Nw-(4-Toluenesulfonyl)-D-arginine for its potential in modulating enzyme activity and its application in various assays, including those aimed at understanding protein interactions and functions. Its ability to serve as a versatile reagent in organic synthesis further underscores its importance in laboratories focused on medicinal chemistry. This compound stands out due to its stability and compatibility with a range of reaction conditions, making it an ideal choice for professionals seeking reliable and effective solutions in their research endeavors.

Synonyms
D-Arg(Tos)-OH
CAS Number
97233-92-6
Purity
≥ 97% (HPLC)
Molecular Formula
C13H20N4O4S
Molecular Weight
328.39
MDL Number
MFCD00236800
PubChem ID
13241834
Melting Point
108-112? C
Optical Rotation
-13º±1º (c=1.121% in HCl)
Conditions
Store at 0-8°C
General Information
Synonyms
D-Arg(Tos)-OH
CAS Number
97233-92-6
Purity
≥ 97% (HPLC)
Molecular Formula
C13H20N4O4S
Molecular Weight
328.39
MDL Number
MFCD00236800
PubChem ID
13241834
Melting Point
108-112? C
Optical Rotation
-13º±1º (c=1.121% in HCl)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Nw-(4-Toluenesulfonyl)-D-arginine is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a valuable tool in studying protein interactions and enzyme activities, particularly in the context of arginine metabolism.
  • Drug Development: It is used in the design of novel pharmaceuticals targeting specific receptors, enhancing the efficacy of drug candidates through its unique sulfonamide group.
  • Peptide Synthesis: The compound is beneficial in synthesizing modified peptides, allowing researchers to explore new therapeutic avenues in areas like cancer treatment and immunology.
  • Diagnostics: It can be employed in developing diagnostic assays that require specific binding interactions, improving the sensitivity and specificity of tests.
  • Antiviral Research: The compound shows potential in antiviral studies, aiding in the exploration of mechanisms to inhibit viral replication, which is crucial in combating infectious diseases.

Citations