2415-43-2

3',5'-UpU Chemical Structure
2415-43-2

Chemical Structure

3',5'-UpU

Synonym(s): 3',5'-Uridylyluridine

  • CAS No.: 2415-43-2
  • Formula:C18H23N4O14P
  • Molecular Weight:550.37

InChIKey: KXSPLNAXPMVUEC-NCOIDOBVSA-N

SMILES: O=C(C=CN1[C@H]2[C@H](O)[C@H](OP(OC[C@H]3O[C@@H](N(C(N4)=O)C=CC4=O)[C@H](O)[C@@H]3O)(O)=O)[C@@H](CO)O2)NC1=O

Biological Activity: 3',5'-UpU (3',5'-Uridylyluridine) is a 3',5'-linked uridylyluridine dinucleotide. 3',5'-UpU undergoes cyclization/cleavage reactions to form uridine and uridine 2',3'-cyclic phosphate, and can also isomerize into 2',5'-UpU. Under the consecutive acid-base bifunctional catalysis of imidazole buffer, 3',5'-UpU undergoes cyclization/cleavage reactions via a phosphorane intermediate[1].

Cat. No. Product Name Purity Description Pricing
HY-159806
3',5'-UpU 3',5'-UpU (3',5'-Uridylyluridine) is a 3',5'-linked uridylyluridine dinucleotide. 3',5'-UpU undergoes cyclization/cleavage reactions to form uridine and uridine 2',3'-cyclic phosphate, and can also isomerize into 2',5'-UpU. Under the consecutive acid-base bifunctional catalysis of imidazole buffer, 3',5'-UpU undergoes cyclization/cleavage reactions via a phosphorane intermediate.
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