65562-44-9 Usage
Description
(5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is a complex organic molecule characterized by its unique structure, which includes a hexopyranosyl group, a nitrophenyl group, and a thiazolidinone ring. (5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is known for its potential medicinal applications, primarily due to the pharmacological activities associated with its thiazolidinone core. Additionally, the presence of the nitrophenyl group suggests that the molecule may exhibit antimicrobial and anticancer properties, making it a promising candidate for drug development and research in the fields of medicine and pharmacology.
Uses
Used in Pharmaceutical Industry:
(5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is used as a potential therapeutic agent for its possible antimicrobial and anticancer properties. (5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one's structure, featuring a thiazolidinone core and a nitrophenyl group, indicates that it may be effective in targeting and treating various types of cancer and microbial infections.
Used in Drug Development Research:
In the field of drug development, (5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one serves as a valuable compound for research purposes. Its unique structure and potential pharmacological activities make it an interesting subject for further investigation, with the aim of understanding its mechanisms of action and optimizing its properties for use in the development of new drugs.
Used in Medicinal Chemistry:
(5Z)-3-hexopyranosyl-5-[(4-nitrophenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is utilized as a key molecule in medicinal chemistry for the design and synthesis of novel therapeutic agents. Its structural features, including the hexopyranosyl group and the nitrophenyl group, provide a foundation for the development of new drugs with enhanced efficacy and selectivity in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-44-9 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 65562-44:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*4)+(1*4)=139
139 % 10 = 9
So 65562-44-9 is a valid CAS Registry Number.
65562-44-9Relevant 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.
