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Home Other Building Blocks 2'-AZIDO-2'-DEOXYCYTIDINE

2'-AZIDO-2'-DEOXYCYTIDINE

CAS No.:
51034-68-5
Catalog Number:
AG00DCDU
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00DCDU
Chemical Name:
2'-AZIDO-2'-DEOXYCYTIDINE
CAS Number:
51034-68-5
MDL Number:
MFCD00043047
IUPAC Name:
4-amino-1-[(2R,3R,4S,5R)-3-azido-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
InChI:
InChI=1S/C9H12N6O4/c10-5-1-2-15(9(18)12-5)8-6(13-14-11)7(17)4(3-16)19-8/h1-2,4,6-8,16-17H,3H2,(H2,10,12,18)/t4-,6-,7-,8-/m1/s1
InChI Key:
FEOYKPQEERVCAV-XVFCMESISA-N
EC Number:
256-927-8
Properties
Complexity:
485  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
268.092g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
268.233g/mol
Monoisotopic Mass:
268.092g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
123A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.1  
Literature
Title Journal
Enantioselectivity of ribonucleotide reductase: a first study using stereoisomers of pyrimidine 2'-azido-2'-deoxynucleosides. Biochemical pharmacology 20040815
Synergistic antiviral action of ribonucleotide reductase inhibitors and 3'-azido-3'-deoxythymidine on HIV type 1 infection in vitro. AIDS research and human retroviruses 19960520
Inhibition of ribonucleotide reductase by 2'-substituted deoxycytidine analogs: possible application in AIDS treatment. Proceedings of the National Academy of Sciences of the United States of America 19940830
Synthesis and antiviral evaluation of carbocyclic analogues of 2'-azido- and 2'-amino-2'-deoxycytidine. Journal of medicinal chemistry 19880201
Antiviral, antimetabolic and antineoplastic activities of 2'- or 3'-amino or -azido-substituted deoxyribonucleosides. Biochemical pharmacology 19800615
Properties