1888-31-9 Usage
Uses
Used in Pharmaceutical Research and Development:
Propanediamide, N-[(4-methylphenyl)sulfonyl]-N'-phenylis used as a research compound for studying the enzyme insulin-regulated aminopeptidase (IRAP) and its role in various biological processes. Its ability to inhibit IRAP makes it a promising candidate for the development of drugs targeting this enzyme.
Used in Diabetes Treatment:
In the healthcare industry, Propanediamide, N-[(4-methylphenyl)sulfonyl]-N'-phenylis used as a potential therapeutic agent for the treatment of diabetes and related metabolic disorders. It modulates insulin signaling and glucose metabolism, offering a novel approach to managing these conditions.
Used in Anti-inflammatory Applications:
Propanediamide, N-[(4-methylphenyl)sulfonyl]-N'-phenylis utilized as an anti-inflammatory agent due to its demonstrated anti-inflammatory properties. This makes it a candidate for the development of drugs targeting inflammation-related conditions.
Used in Anti-cancer Applications:
In the field of oncology, Propanediamide, N-[(4-methylphenyl)sulfonyl]-N'-phenylis used as a potential anti-cancer agent. Its anti-cancer properties are being investigated for the development of drugs that could target various types of cancer.
Used in Drug Discovery and Development:
Propanediamide, N-[(4-methylphenyl)sulfonyl]-N'-phenylis employed as a target in drug discovery and development due to its multifaceted properties, including its potential in treating diabetes, inflammation, and cancer. Its diverse applications make it a valuable compound for the creation of innovative pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 1888-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1888-31:
(6*1)+(5*8)+(4*8)+(3*8)+(2*3)+(1*1)=109
109 % 10 = 9
So 1888-31-9 is a valid CAS Registry Number.
1888-31-9Relevant academic research and scientific papers
Triple equilibrium in n′-aryl-n-tosyldiazomalonimidolates, 1-tosyl-1,2,3-triazol-5-olates, and 1-aryl-1,2,3-triazol-5-olates
Morzherin,Rozin,Savel'eva,Bakulev
, p. 168 - 173 (2007/10/03)
A series of 1-tosyl-substituted 4-arylcarbamoyl-1,2,3-triazol-2-olates, which can undergo rearrangement to isomeric 1-aryl-4-tosylcarbamoyl-1,2,3-triazol-5-olates and N-tosyl-N′-aryldiazomalonimidolates, were synthesized. An equilibrium between these comp
