(R-P)-[17-O,18-O]-URIDYLYL-3'->5'-ADENOSINE
Compound with spectra: 2 NMR
![(R-P)-[17-O,18-O]-URIDYLYL-3'->5'-ADENOSINE](/api/compound/BJSWyK3Am4P.png?ph=true&h=300&w=458 "(R-P)-[17-O,18-O]-URIDYLYL-3'->5'-ADENOSINE")
| SpectraBase Compound ID | BJSWyK3Am4P |
|---|---|
| InChI | InChI=1S/C19H24N7O12P/c20-15-10-16(22-5-21-15)26(6-23-10)17-12(30)11(29)8(37-17)4-35-39(33,34)38-14-7(3-27)36-18(13(14)31)25-2-1-9(28)24-19(25)32/h1-2,5-8,11-14,17-18,27,29-31H,3-4H2,(H,33,34)(H2,20,21,22)(H,24,28,32)/t7-,8-,11-,12-,13-,14-,17-,18-/m0/s1 |
| InChIKey | SWTWQWKNQDDGCS-FOHSIVBMSA-N |
| Mol Weight | 573.41 g/mol |
| Molecular Formula | C19H24N7O12P |
| Exact Mass | 573.122056 g/mol |
| Enantiomer InChIKey | SWTWQWKNQDDGCS-KPKSGTNCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | 100MM-EDTA;25%-D2O;PH=8 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | 100MM-EDTA;25%-D2O;PH=8 |
5'-O-(URIDIN-3'-YLOXYTHIOPHOSPHORYL)ADENOSINE (DIASTEREOMER MIXTURE)
(R-P)-URIDYLYL-(3'->5')-N(1)-METHYLADENOSINE-METHYLESTER
P1-5'-O-ADENOSINE-P4-5'-O-URIDINE-TETRAPHOSPHATE-SODIUM-SALT
P1-5'-O-ADENOSINE-P3-5'-O-URIDINE-TRIPHOSPHATE-SODIUM-SALT
P1-5'-O-ADENOSINE-P3-5'-O-THYMIDINE-TRIPHOSPHATE-SODIUM-SALT
5'-(3'-AMINO-3'-DEOXYCYTIDIN-3'-YLPHOSPHORYL)-3'-AMINO-3'-DEOXYADENOSINE
P1-5'-O-ADENOSINE-P3-5'-O-CYTIDINE-TRIPHOSPHATE-SODIUM-SALT
4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin
ADENYLYL-(2'->5')-ADENOSINE, ADENYLYL-(2'->5')ADENOSINE
ADENOSINE-3',5'-CYCLOPHOSPHATE-2'-BETA-CYANOETHYLPHOSPHATE
| Title | Journal or Book | Year |
|---|---|---|
| Oxygen chiral phosphate in uridylyl(3'.fwdarw.5')adenosine by oxidation of a phosphite intermediate: synthesis and absolute configuration | Journal of the American Chemical Society | 1983 |