65562-37-0 Usage
Description
(5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is a complex organic molecule characterized by its thiazolidine and pyridine structures. It features a thioxo group and is substituted with acetylhexopyranosyl groups, making it a thiazolidin-4-one derivative. (5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one holds potential biological and pharmacological activities, with its pyridinylmethylidene and acetylhexopyranosyl groups suggesting possible applications in medicinal chemistry, particularly in the development of novel drug molecules. The intricate nature of this compound implies it may possess unique properties and potential uses across various scientific and medical fields.
Uses
Used in Pharmaceutical Industry:
(5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential candidate for drug development due to its complex structure and the presence of biologically active groups. Its unique molecular composition may allow for the targeting of specific receptors or enzymes, making it a promising compound for the creation of new medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, this compound is used as a starting point for the synthesis of new drug molecules. The presence of the thiazolidin-4-one core and the pyridinylmethylidene and acetylhexopyranosyl substituents may provide a foundation for the design of molecules with specific therapeutic properties, such as improved binding affinity, selectivity, and bioavailability.
Used in Chemical Synthesis:
(5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one can be utilized as an intermediate in the synthesis of other complex organic molecules. Its unique structure may facilitate the development of new synthetic routes and methodologies, contributing to the advancement of chemical synthesis techniques.
Used in Biological Research:
(5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one may also find applications in biological research, where it can be employed to study the interactions between small molecules and biological targets, such as proteins or nucleic acids. (5Z)-5-(pyridin-3-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's structure may allow for the investigation of various biological processes and the development of new tools for understanding complex biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-37-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 65562-37:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*7)=140
140 % 10 = 0
So 65562-37-0 is a valid CAS Registry Number.
65562-37-0Relevant articles and documents
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.
