65562-42-7 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-5-(1H-indol-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential pharmaceutical agent for its diverse biological activities. The indole group within the compound is known to contribute to antiviral, anticancer, and antimicrobial properties, making it a promising candidate for the development of new drugs targeting these areas.
Additionally, the thiazolidinone ring suggests potential for anti-inflammatory, antioxidant, and antitumor activities, further expanding the compound's applicability in medicinal chemistry. The presence of acetyl groups may enhance the solubility of the compound, which is a critical factor in drug development for improving bioavailability and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-42-7 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, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65562-42:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*4)+(1*2)=137
137 % 10 = 7
So 65562-42-7 is a valid CAS Registry Number.
65562-42-7Relevant 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.
