65562-24-5 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-5-[(2,5-dimethoxyphenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a pharmaceutical candidate for its potential antiviral, antibacterial, antifungal, and antitumor effects due to its thiazolidine core and functional groups.
Used in Drug Development:
(5Z)-5-[(2,5-dimethoxyphenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a compound in drug development to explore its potential as a therapeutic agent, leveraging its diverse biological properties and the benefits of its acetyl groups for improved solubility, stability, and pharmacokinetics.
Used in Research:
(5Z)-5-[(2,5-dimethoxyphenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a subject of research to further investigate its biological activities and potential applications in medicine, given its complex structure and the known bioactivities of thiazolidine derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-24-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 65562-24:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*4)=135
135 % 10 = 5
So 65562-24-5 is a valid CAS Registry Number.
65562-24-5Relevant 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.
