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Home  > Inhibitors/Agonists  > Cell Cycle  > Nucleoside Antimetabolite/Analog  > 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one

AB45830

147-94-4 | 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $3.00 $2.00 -   +
1g 98% in stock $12.00 $8.00 -   +
5g 98% in stock $13.00 $9.00 -   +
25g 98% in stock $55.00 $39.00 -   +
100g 98% in stock $190.00 $133.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AB45830
Chemical Name: 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one
CAS Number: 147-94-4
Molecular Formula: C9H13N3O5
Molecular Weight: 243.2166
MDL Number: MFCD00066487
SMILES: OC[C@H]1O[C@H]([C@H]([C@@H]1O)O)n1ccc(nc1=O)N

 

Computed Properties
Complexity: 383  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 2  
XLogP3: -2.1  

 

 

Upstream Synthesis Route 
  • Cytosine β-D-arabinofuranoside is a valuable compound widely utilized in chemical synthesis for its ability to serve as a building block in the creation of nucleoside analogs. This versatile molecule plays a crucial role in the development of novel pharmaceuticals and biologically active compounds through its incorporation into DNA and RNA structures. With its unique chemical structure, Cytosine β-D-arabinofuranoside offers researchers a powerful tool for designing and synthesizing new molecules with targeted biological activities. Its applications in chemical synthesis extend to various fields, including medicinal chemistry, drug discovery, and bioorganic chemistry, where precise control over nucleoside modifications is essential for achieving desired therapeutic outcomes. By harnessing the reactivity and structural flexibility of Cytosine β-D-arabinofuranoside, chemists can unlock new possibilities in the design and synthesis of innovative molecular entities with enhanced pharmacological properties.
Literature
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