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CAS 3736-77-4

:

2,2′-Anhydrouridine

Description:
2,2′-Anhydrouridine, with the CAS number 3736-77-4, is a nucleoside analog derived from uridine. It is characterized by the absence of the hydroxyl group at the 2' position of the ribose sugar, which results in a unique structural configuration that influences its biochemical properties. This compound is typically a white to off-white solid and is soluble in water, making it suitable for various biological applications. 2,2′-Anhydrouridine is known for its role in nucleic acid research and has been studied for its potential antiviral and anticancer properties. Its structural modifications allow it to interact with nucleic acids and enzymes, potentially inhibiting certain biological processes. The compound's stability and reactivity can vary depending on environmental conditions, such as pH and temperature. Overall, 2,2′-Anhydrouridine serves as an important tool in molecular biology and medicinal chemistry, contributing to the understanding of nucleoside function and the development of therapeutic agents.
Formula:C9H10N2O5
InChI:InChI=1S/C9H10N2O5/c12-3-4-6(14)7-8(15-4)11-2-1-5(13)10-9(11)16-7/h1-2,4,6-8,12,14H,3H2/t4-,6-,7+,8-/m1/s1
InChI key:InChIKey=UUGITDASWNOAGG-CCXZUQQUSA-N
SMILES:O[C@H]1[C@]2([C@](N3C(O2)=NC(=O)C=C3)(O[C@@H]1CO)[H])[H]
Synonyms:
  • (2R,3R,3aR,9aR)-3-hydroxy-2-(hydroxymethyl)-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5][1,3]oxazolo[3,2-a]pyrimidin-6-one
  • (2R,3R,3aS,9aR)-2,3,3a,9a-Tetrahydro-3-hydroxy-2-(hydroxymethyl)-6H-furo[2′,3′:4,5]oxazolo[3,2-a]pyrimidin-6-one
  • (2R,3R,3aS,9aR)-3-hydroxy-2-(hydroxymethyl)-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5][1,3]oxazolo[3,2-a]pyrimidin-6-one
  • 02,2-Cycloridine
  • 2,2'-Anhydro-uridine
  • 2,2'-O-Anhydro-(1-β-D-arabinofuranosyl)uracil
  • 2,2-Anhydro-1-(b-D-Arabinofuranosyl) Uracil
  • 2,2-Anhydrocytidine
  • 2,2′-Anhydro(1-β-<span class="text-smallcaps">D</span>-arabinofuranosyl)uracil
  • 2,2′-Anhydro-1-β-<span class="text-smallcaps">D</span>-arabino-furanosyluracil
  • See more synonyms
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