127559-73-3 Usage
Chemical compound
A substance formed by a chemical reaction, consisting of a specific arrangement of atoms.
Used in development of nucleoside analogs
Nucleoside analogs are molecules that resemble the structure of nucleosides, the building blocks of DNA and RNA, and are used in antiviral and anticancer therapies.
Antiviral and anticancer therapies
These therapies aim to treat viral infections and cancer by targeting specific cells or processes involved in the disease.
Thymine derivative
A molecule that is structurally similar to thymine, one of the four nucleobases in DNA.
Azido group
A functional group with the formula N3, which provides a site for bioorthogonal conjugation reactions.
Bioorthogonal conjugation reactions
Chemical reactions that occur selectively in the presence of other functional groups without interfering with them.
Modification for various applications
The azido group allows for the attachment of other molecules or groups to the compound, enabling its use in different applications.
Hydroxymethyl ethoxy functional group
A functional group with the formula CH2OCH2CH2OH, which is important for the antiviral and anticancer properties of the compound.
Targeting specific viral and cancerous cells
The compound has shown promise in selectively targeting and affecting specific cells involved in viral infections and cancer, making it a valuable asset in medical research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 127559-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127559-73:
(8*1)+(7*2)+(6*7)+(5*5)+(4*5)+(3*9)+(2*7)+(1*3)=153
153 % 10 = 3
So 127559-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N5O4/c1-6-3-14(9(17)12-8(6)16)5-18-7(4-15)2-11-13-10/h3,7,15H,2,4-5H2,1H3,(H,12,16,17)
127559-73-3Relevant articles and documents
Synthesis of biologically active acycloazt derivatives and related compounds
Murata,Achiwa
, p. 836 - 838 (1990)
The synthesis of optically active acyclic analogues of 3'-azido-3'-deoxythymidine, which lack only the 2'-CH2 of the sugar, is described. The synthesis of some nucleoside analogues that contain the N-acetyl-D-neuraminic acid moiety is also described.
