4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin
Compound with spectra: 1 NMR
![4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin](/api/compound/2PQMbhxIuOT.png?ph=true&h=300&w=458 "4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin")
| SpectraBase Compound ID | 2PQMbhxIuOT |
|---|---|
| InChI | InChI=1S/C21H20N5O9P/c1-30-11-2-3-13-12(5-11)10(4-15(27)33-13)6-31-36(29)32-7-14-18(35-36)17(28)21(34-14)26-9-25-16-19(22)23-8-24-20(16)26/h2-5,8-9,14,17-18,21,28H,6-7H2,1H3,(H2,22,23,24)/t14-,17-,18-,21-,36+/m1/s1 |
| InChIKey | QUYVRKGPKPPWQC-GFGFNENVSA-N |
| Mol Weight | 517.39 g/mol |
| Molecular Formula | C21H20N5O9P |
| Exact Mass | 517.099864 g/mol |
| Enantiomer InChIKey | QUYVRKGPKPPWQC-NYNIZWMASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-7-dimethylamino-coumarin
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]-7-dimethylamino-coumarin
VILPZALHFBLWBO-ONMZBTRXSA-N
ADENOSINE-3',5'-CYCLIC-[R-(P)]-[4-[N,N-BIS-(2-(TRIMETHYLSILYL)-ETHOXYCARBONYLMETHYL)-CARBAMOYL]-2-NITROPHENYL]-METHYL-PHOSPHONATE
ADENOSINE-3',5'-CYCLIC-[S-(P)]-[4-[N,N-BIS-(2-(TRIMETHYLSILYL)-ETHOXYCARBONYLMETHYL)-CARBAMOYL]-2-NITROPHENYL]-METHYL-PHOSPHONATE
2'-O-TERT.-BUTYL-DIMETHYLSILYL-5'-O-PARA-METHOXYTRITYL-ADENOSINE-DIETHYL-3'-PHOSPHATE
(R-P)-URIDYLYL-(3'->5')-N(1)-METHYLADENOSINE-METHYLESTER
(R-P)-[17-O,18-O]-URIDYLYL-3'->5'-ADENOSINE
5'-O-(URIDIN-3'-YLOXYTHIOPHOSPHORYL)ADENOSINE (DIASTEREOMER MIXTURE)
| Title | Journal or Book | Year |
|---|---|---|
| Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 2. Photocleavage of Selected (Coumarin-4-yl)methyl-Caged Adenosine Cyclic 3‘,5‘-Monophosphates with Fluorescence Enhancement | The Journal of Organic Chemistry | 2002 |