15648-73-4
Chemical Structure
5′-O-Phosphonocytidylyl-(3′→5′)-adenosine
- CAS No.: 15648-73-4
- Formula:C19H26N8O14P2
- Molecular Weight:652.40
InChIKey: MMTJWPKMSKNVDK-KPKSGTNCSA-N
SMILES: NC(C=CN1[C@H]2[C@H](O)[C@H](OP(OC[C@H]3O[C@@H](N(C=N4)C5=C4C(N)=NC=N5)[C@H](O)[C@@H]3O)(O)=O)[C@@H](COP(O)(O)=O)O2)=NC1=O
Biological Activity: 5′-O-Phosphonocytidylyl-(3′→5′)-adenosine is a diribonucleotide. 5′-O-Phosphonocytidylyl-(3′→5′)-adenosine can be isolated from embryos of the copepod Euchaeta japonica Marukawa[1].
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5′-O-Phosphonocytidylyl-(3′→5′)-adenosine | 5′-O-Phosphonocytidylyl-(3′→5′)-adenosine is a diribonucleotide. 5′-O-Phosphonocytidylyl-(3′→5′)-adenosine can be isolated from embryos of the copepod Euchaeta japonica Marukawa. | |||||||||||||||||||||
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- [1]. Hepner AS, et al. Isolation of cytidylyl-(5'+3')-adenosine-5' phosphate (pApC), adenylyl-(5'+3')-cytidine-5' phosphate (pCpA), uridylyl-(5'+3')-adenosine-5' phosphate (pApU) and adenylyl-(5'+3')-uridine-5' phosphate (pUpA) from embryos of the copepod Euchaeta japonica Marukawa. Biochem Biophys Res Commun. 1967 Mar 9;26(5):584-9. [Content Brief]