65929-46-6 Usage
Description
(5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is a complex organic molecule characterized by the presence of a thiazolidine ring, a pyridine group, and multiple acetyl groups. It features a thioxo group and a hexopyranosyl group attached to the thiazolidine ring, which may contribute to its potential pharmaceutical applications. (5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's structural features, including the thioxo and thiazolidin-4-one groups, suggest it may possess anti-inflammatory or antiviral properties. Additionally, the pyridine group could indicate its potential as a bioactive molecule, making it a promising candidate for drug development and research in medicinal chemistry.
Uses
Used in Pharmaceutical Applications:
(5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential candidate for drug development due to its unique structural features and the presence of bioactive groups such as the thioxo and thiazolidin-4-one groups. These groups may contribute to its potential anti-inflammatory or antiviral properties, making it a valuable compound for further study and development in the pharmaceutical industry.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a biochemical tool for studying its potential applications and interactions with biological systems. (5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's intricate structure, including the pyridine group, presents opportunities for exploring its bioactivity and potential as a therapeutic agent.
Used in Drug Delivery Systems:
(5Z)-5-(pyridin-4-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one may also be utilized in the development of novel drug delivery systems. Its structural features could be harnessed to improve the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical agents, particularly in the context of targeted drug delivery and controlled release applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65929-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,2 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65929-46:
(7*6)+(6*5)+(5*9)+(4*2)+(3*9)+(2*4)+(1*6)=166
166 % 10 = 6
So 65929-46-6 is a valid CAS Registry Number.
65929-46-6Relevant articles and documents
N glucopyranosyl 5 aralkylidenerhodanines: Synthesis and antibacterial and antiviral activities
Foye,Tovivich
, p. 1607 - 1611 (2007/10/08)
A series of N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-aralkylidenerhodanines was synthesized, and the acetyl groups were removed to give N-β-D-glucopyranosyl-5-aralkylidenerhodanines without cleavage of the rhodanine ring by means of acid hydrolysis. Alkaline hydrolysis with ammonia in methanol resulted in cleavage to N-glucosylthiourea, providing evidence for N-glycoside formation. A number of the rhodanine derivatives, especially those with nitro or chloro groups in the aromatic ring, showed antibacterial activity. N-β-D-Glucopyranosyl-5-(4-nitrobenzylidene)rhodanine showed antiviral activity by inhibition of viral RNA synthesis. Some effect on blood sugar levels also was observed with several rhodanines.
