65562-30-3 Usage
Uses
Used in Medicinal Chemistry:
(5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is utilized as a compound of interest in medicinal chemistry due to its unique structure and potential biological activities. Its thioxo and thiazolidin functionalities may contribute to its interaction with biological targets, making it a candidate for the development of new therapeutic agents.
Used in Drug Development:
In the field of drug development, (5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is considered for its potential as a lead compound. (5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's acetylhexopyranosyl group may enhance its solubility and cellular uptake, which are crucial factors in the effectiveness of a drug. Further research and development could lead to the creation of novel pharmaceuticals based on (5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's structure and properties.
Used in Pharmaceutical Industry:
(5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a research molecule in the pharmaceutical industry for its potential to contribute to the discovery of new drugs. Its unique chemical features and the possibility of it being a glycoside or carbohydrate derivative make it a valuable asset in the search for innovative therapeutic solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-30-3 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, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65562-30:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*0)=133
133 % 10 = 3
So 65562-30-3 is a valid CAS Registry Number.
65562-30-3Relevant 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.
