65562-22-3 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-5-(1,3-benzodioxol-5-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential pharmaceutical candidate due to its complex molecular structure and the presence of various functional groups that may interact with biological targets.
Used in Biochemical Research:
In the field of biochemical research, (5Z)-5-(1,3-benzodioxol-5-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used for exploring its potential interactions with biological targets, which could lead to the discovery of new therapeutic agents or a better understanding of biological processes.
Used in Drug Development:
(5Z)-5-(1,3-benzodioxol-5-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's unique structure, including the thiazolidin-4-one ring, suggests it may have antidiabetic, anti-inflammatory, or antiviral properties, making it a valuable asset in the development of new drugs targeting these conditions.
Used in Medicinal Chemistry:
(5Z)-5-(1,3-benzodioxol-5-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used in medicinal chemistry for further exploration of its potential applications, including the development of novel therapeutic agents and the enhancement of existing drugs through structural modifications.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65562-22:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*2)=133
133 % 10 = 3
So 65562-22-3 is a valid CAS Registry Number.
65562-22-3Relevant academic research and scientific papers
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.
