sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks 5'-DEOXYTHYMIDINE

5'-DEOXYTHYMIDINE

CAS No.:
3458-14-8
Catalog Number:
AG00C0Q1
Molecular Formula:
C10H14N2O4
Molecular Weight:
226.2292
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
≥95%
1 week
United States
$91
- +
5mg
≥95%
1 week
United States
$187
- +
10mg
≥95%
1 week
United States
$300
- +
Product Description
Catalog Number:
AG00C0Q1
Chemical Name:
5'-DEOXYTHYMIDINE
CAS Number:
3458-14-8
Molecular Formula:
C10H14N2O4
Molecular Weight:
226.2292
MDL Number:
MFCD07779404
IUPAC Name:
1-[(2R,4S,5R)-4-hydroxy-5-methyloxolan-2-yl]-5-methylpyrimidine-2,4-dione
InChI:
InChI=1S/C10H14N2O4/c1-5-4-12(10(15)11-9(5)14)8-3-7(13)6(2)16-8/h4,6-8,13H,3H2,1-2H3,(H,11,14,15)/t6-,7+,8-/m1/s1
InChI Key:
UGUILUGCFSCUKR-GJMOJQLCSA-N
SMILES:
O[C@H]1C[C@@H](O[C@@H]1C)n1cc(C)c(=O)[nH]c1=O
Properties
Complexity:
366  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Defined Bond Stereocenter Count:
0
Exact Mass:
226.095g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
226.232g/mol
Monoisotopic Mass:
226.095g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
78.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7  
Literature
Title Journal
Formation of aminyl radicals on electron attachment to AZT: abstraction from the sugar phosphate backbone versus one-electron oxidation of guanine. The journal of physical chemistry. B 20100722
Kinetic parameters and recognition of thymidine analogues with varying functional groups by thymidine phosphorylase. Bioorganic & medicinal chemistry 20080401
Study on reactivity and protection of the alpha-hydroxyphosphonate moiety in 5'-nucleotide analogues: formation of the 3'-O-P-C(OH)-C4' internucleotide linkage. Nucleosides, nucleotides & nucleic acids 20030301
Synthesis and HIV-1 reverse transcriptase inhibitor activity of some 2,5,6-substituted benzoxazole, benzimidazole, benzothiazole and oxazolo(4,5-b)pyridine derivatives. Arzneimittel-Forschung 20030101
A-hydroxyphosphonate oligonucleotides: a promising DNA type? Nucleosides, nucleotides & nucleic acids 20030101
Properties