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Home Other Building Blocks 6-Chloropurine ribonucleoside

6-Chloropurine ribonucleoside

CAS No.:
2004-06-0
Catalog Number:
AG002CQY
Molecular Formula:
C10H11ClN4O4
Molecular Weight:
286.6717
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%(HPLC)
In Stock USA
United States
$39
- +
5g
98%(HPLC)
In Stock USA
United States
$66
- +
25g
98%(HPLC)
In Stock USA
United States
$150
- +
100g
98%(HPLC)
In Stock USA
United States
$465
- +
Product Description
Catalog Number:
AG002CQY
Chemical Name:
6-Chloropurine ribonucleoside
CAS Number:
2004-06-0
Molecular Formula:
C10H11ClN4O4
Molecular Weight:
286.6717
MDL Number:
MFCD00005738
IUPAC Name:
(2R,3R,4S,5R)-2-(6-chloropurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
InChI:
InChI=1S/C10H11ClN4O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2/t4-,6-,7-,10-/m1/s1
InChI Key:
XHRJGHCQQPETRH-KQYNXXCUSA-N
SMILES:
OC[C@H]1OC([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2Cl
Properties
Complexity:
339  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
286.047g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
286.672g/mol
Monoisotopic Mass:
286.047g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
114A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.3  
Literature
Title Journal
Biosynthesis of anti-HCV compounds using thermophilic microorganisms. Bioorganic & medicinal chemistry letters 20121001
Suzuki-miyaura and sonogashira coupling of 6-chloropurines and -nucleosides in water. Organic letters 20090618
5'-O-masked 2'-deoxyadenosine analogues as lead compounds for hepatitis C virus (HCV) therapeutic agents. Bioorganic & medicinal chemistry 20071115
Synthesis and biological evaluation of nucleoside analogues having 6-chloropurine as anti-SARS-CoV agents. Bioorganic & medicinal chemistry letters 20070501
Introduction of a benzyl group onto the 2'-OH of 6-chloropurine 3'-O-benzoylriboside. Nucleosides, nucleotides & nucleic acids 20030101
Anti-malarial activity of N(6)-substituted adenosine derivatives. Part I. Bioorganic & medicinal chemistry 20020301
Synthesis and antiviral activity of carbocyclic analogues of 2'-deoxyribofuranosides of 2-amino-6-substituted-purines and of 2-amino-6-substituted-8-azapurines. Journal of medicinal chemistry 19841101
Synthesis and antiviral activity of certain carbamoylpyrrolopyrimidine and pyrazolopyrimidine nucleosides. Journal of medicinal chemistry 19821101
Synthesis and antiviral activity of certain 9-beta-D-ribofuranosylpurine-6-carboxamides. Journal of medicinal chemistry 19810801
Purine analogs as potential anticytomegalovirus agents. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) 19690901
Properties