65562-31-4 Usage
Uses
Used in Pharmaceutical Applications:
(5Z)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-5-(thiophen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one is used as a potential drug candidate for its anti-inflammatory and anti-cancer properties due to its thiazolidin-4-one structural motif.
Used in Drug Development:
In the pharmaceutical industry, (5Z)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-5-(thiophen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one is used as a compound for further research and study to fully understand its chemical and biological properties, with the aim of developing new therapeutic agents.
Used in Bioavailability Enhancement:
(5Z)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-5-(thiophen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one is used as a compound to explore its potential in improving the bioavailability of pharmaceuticals, possibly through its carbohydrate moiety, which may influence pharmacokinetic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-31-4 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, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65562-31:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*1)=134
134 % 10 = 4
So 65562-31-4 is a valid CAS Registry Number.
65562-31-4Relevant 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.
