3736-77-4
3736-77-4
Chemical Structure
2,2'-Anhydrouridine
Synonym(s): 2,2'-Cyclouridine; O2,2'-Cyclouridine
- CAS No.: 3736-77-4
- Formula:C9H10N2O5
- Molecular Weight:226.19
IUPAC Name: (2R,3R,3aS,9aR)-3-hydroxy-2-(hydroxymethyl)-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-6-one
InChIKey: UUGITDASWNOAGG-CCXZUQQUSA-N
SMILES: OC[C@@H](O1)[C@@H](O)[C@@](O2)([H])[C@]1([H])N(C2=N3)C=CC3=O
Biological Activity: 2,2'-Anhydrouridine (2,2'-Cyclouridine) is a nucleoside analog. 2,2'-Anhydrouridine is an important intermediate in the synthesis of other nucleoside-related compounds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2,2'-Anhydrouridine | 99.66% | 2,2'-Anhydrouridine (2,2'-Cyclouridine) is a nucleoside analog. 2,2'-Anhydrouridine is an important intermediate in the synthesis of other nucleoside-related compounds. | ||||||||||||||||||||
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References
- [1]. Drabikowska AK, et al. Inhibitor properties of some 5-substituted uracil acyclonucleosides, and 2,2'-anhydrouridines versus uridine phosphorylase from E. coli and mammalian sources. Biochem Pharmacol. 1987 Dec 1;36(23):4125-8. [Content Brief]
- [2]. Mercer J R, et al. An improved synthesis of 14C-labelled 2, 2′-anhydrouridine, 2′-deoxyuridine and 5-ethyl-2′-deoxyuridine[J]. International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1986, 37(7): 613-619.
