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Home Aminos Uridine, 2'-amino-2'-deoxy-

Uridine, 2'-amino-2'-deoxy-

CAS No.:
26889-39-4
Catalog Number:
AG00I536
Molecular Formula:
C9H13N3O5
Molecular Weight:
243.2166
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Product Description
Catalog Number:
AG00I536
Chemical Name:
Uridine, 2'-amino-2'-deoxy-
CAS Number:
26889-39-4
Molecular Formula:
C9H13N3O5
Molecular Weight:
243.2166
MDL Number:
MFCD01317284
IUPAC Name:
1-[(2R,3R,4S,5R)-3-amino-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
InChI:
InChI=1S/C9H13N3O5/c10-6-7(15)4(3-13)17-8(6)12-2-1-5(14)11-9(12)16/h1-2,4,6-8,13,15H,3,10H2,(H,11,14,16)/t4-,6-,7-,8-/m1/s1
InChI Key:
LLIPTMWIZVIUSX-XVFCMESISA-N
SMILES:
OC[C@H]1O[C@H]([C@@H]([C@@H]1O)N)n1ccc(=O)[nH]c1=O
Properties
Complexity:
372  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
243.086g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
243.219g/mol
Monoisotopic Mass:
243.086g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
125A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-2.2  
Literature
Title Journal
S-Adenosylhomocysteine hydrolase of the protozoan parasite Trichomonas vaginalis: potent inhibitory activity of 9-(2-deoxy-2-fluoro-β,D-arabinofuranosyl)adenine. Bioorganic & medicinal chemistry letters 20120615
Porphyrin conjugated to DNA by a 2'-amido-2'-deoxyuridine linkage. Bioorganic & medicinal chemistry letters 20080115
Effective modulation of DNA duplex stability by reversible transition metal complex formation in the minor groove. Journal of the American Chemical Society 20070801
DNA and LNA oligonucleotides containing N2'-functionalised derivatives of 2'-amino-2'-deoxyuridine. Bioorganic & medicinal chemistry letters 20060615
[Monomers for oligonucleotide synthesis with linkers carrying reactive residues: II. Synthesis of phosphoamidites based of uridine and cytosine and containing a linker with methoxyoxalamide groups in position 2']. Bioorganicheskaia khimiia 20040101
Synthesis of 2'-modified oligodeoxynucleotides via on-column conjugation. The Journal of organic chemistry 20010126
Antiviral, antimetabolic and antineoplastic activities of 2'- or 3'-amino or -azido-substituted deoxyribonucleosides. Biochemical pharmacology 19800615
Properties