N-[4-Amino-2-chloro-6-[(2-deoxy-2-fluoro-β-D-arabinopyranosyl)amino]-5-pyrimidinyl]-formamide

• CAT Number: R025921
• CAS Number: 1140251-33-7
• Molecular Formula: C10H13ClFN5O4
• Molecular Weight: 321.69
• Purity: ≥95%
• Synonyms: N-(4-Amino-2-chloro-6-(((2R,3S,4R,5R)-3-fluoro-4,5-dihydroxytetrahydro-2H-pyran-2-yl)amino)pyrimidin-5-yl)formamide
• Storage: Store at -20C
• IUPAC Name: N-[4-amino-2-chloro-6-[[(2R,3S,4R,5R)-3-fluoro-4,5-dihydroxyoxan-2-yl]amino]pyrimidin-5-yl]formamide
• InChI: InChI=1S/C10H13ClFN5O4/c11-10-15-7(13)5(14-2-18)8(17-10)16-9-4(12)6(20)3(19)1-21-9/h2-4,6,9,19-20H,1H2,(H,14,18)(H3,13,15,16,17)/t3-,4+,6-,9-/m1/s1
• InChIKey: GIFVSTNLGMIVGT-AYQXTPAHSA-N
• SMILES: C1C(C(C(C(O1)NC2=NC(=NC(=C2NC=O)N)Cl)F)O)O

N-[4-Amino-2-chloro-6-[(2-deoxy-2-fluoro-β-D-arabinopyranosyl)amino]-5-pyrimidinyl]-formamide（Cat No.:R025921）is a specialized compound widely used in pharmaceutical research, particularly in the study of antiviral and anticancer agents. This nucleoside analog, featuring a fluorinated sugar moiety and a chlorinated pyrimidine ring, is crucial for investigating mechanisms of drug resistance and DNA synthesis inhibition. Its unique structure allows it to serve as a potent inhibitor in various biochemical pathways, making it an essential tool for drug development and molecular biology research.