92423-68-2 Usage
Description
5-[(5-bromo-1H-indol-3-yl)methylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-ylacetic acid is a complex organic compound characterized by a 1,3-thiazolidine core structure, featuring a thioxo group and a bromo-substituted indole moiety. This molecule also possesses a carboxylic acid functional group, which endows it with potential as a drug candidate or biochemical reagent. Its intricate structure suggests that it may exhibit a variety of biological activities and interactions with other molecules, rendering it a promising compound for further research and possible applications in the pharmaceutical and chemical biology sectors.
Uses
Used in Pharmaceutical Industry:
5-[(5-bromo-1H-indol-3-yl)methylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-ylacetic acid is used as a potential drug candidate due to its complex structure and the presence of a carboxylic acid functional group. Its ability to interact with other molecules may lead to the development of new therapeutic agents.
Used in Chemical Biology Research:
In the field of chemical biology, 5-[(5-bromo-1H-indol-3-yl)methylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-ylacetic acid serves as a valuable compound for studying its interactions with biological molecules. This research could provide insights into its potential applications in targeting specific biological pathways or as a tool for understanding molecular mechanisms.
Used in Drug Design and Development:
5-[(5-bromo-1H-indol-3-yl)methylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-ylacetic acid's unique structural features make it a candidate for drug design and development. It can be used as a starting point for creating new molecules with improved pharmacological properties, potentially leading to the discovery of novel therapeutics.
Used in Biochemical Reagent Applications:
Given its complex structure and functional groups, 5-[(5-bromo-1H-indol-3-yl)methylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-ylacetic acid can be employed as a biochemical reagent in various laboratory settings. It may be utilized in the synthesis of other complex molecules or in assays designed to study its interactions with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 92423-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,2 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92423-68:
(7*9)+(6*2)+(5*4)+(4*2)+(3*3)+(2*6)+(1*8)=132
132 % 10 = 2
So 92423-68-2 is a valid CAS Registry Number.
