22882-18-4 Usage
Uses
Used in Antiviral Applications:
1-(2-Deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyridinone is used as an antiviral agent for its inhibitory effects on a wide range of viruses, including herpes simplex virus, human cytomegalovirus, and human immunodeficiency virus. Its unique structure allows it to interfere with viral replication and reduce the severity of viral infections.
Used in Antitumor Applications:
In the field of oncology, 1-(2-Deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyridinone is used as an antitumor agent due to its demonstrated cytotoxic activity against various cancer cell lines. It has the potential to be developed into a novel therapeutic for cancer treatment, targeting and destroying cancer cells while minimizing damage to healthy cells.
Used in Pharmaceutical Industry:
1-(2-Deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyridinone is used as a key compound in the development of novel therapeutics for both antiviral and antitumor applications. Its unique structure and demonstrated effectiveness make it a promising candidate for further research and potential integration into new drugs to combat viral infections and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 22882-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22882-18:
(7*2)+(6*2)+(5*8)+(4*8)+(3*2)+(2*1)+(1*8)=114
114 % 10 = 4
So 22882-18-4 is a valid CAS Registry Number.
22882-18-4Relevant academic research and scientific papers
Glycosylations of Ambident Anions of 2(1H)- and 4(1H)-Pyridone and Stereoselective Synthesis of 2(1H)-Pyrimidinone N-(2'-Deoxy-α-D-ribofuranoside)
Seela, Frank,Bindig, Uwe
, p. 895 - 902 (2007/10/02)
Glycosylation of the ambident anions of 2(1H)-pyridone (6) and 4(1H)-pyridone (11) in the presence of KOH with 2-deoxy-3,5-di-O-(p-toluoyl)-α-D-erythro-pentofuranosyl chloride (7) stereoselectively yielded the β-D-O-glycosides 8 and 12, together with anom
