4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]coumarin
Compound with spectra: 1 NMR
![4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]coumarin](/api/compound/HRYqjsYvZPi.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]coumarin")
| SpectraBase Compound ID | HRYqjsYvZPi |
|---|---|
| InChI | InChI=1S/C20H18N5O8P/c21-18-15-19(23-8-22-18)25(9-24-15)20-16(27)17-13(32-20)7-30-34(28,33-17)29-6-10-5-14(26)31-12-4-2-1-3-11(10)12/h1-5,8-9,13,16-17,20,27H,6-7H2,(H2,21,22,23)/t13-,16-,17-,20-,34+/m1/s1 |
| InChIKey | DFZILPQHSXNRKO-YWAOMXHFSA-N |
| Mol Weight | 487.36 g/mol |
| Molecular Formula | C20H18N5O8P |
| Exact Mass | 487.0893 g/mol |
| Enantiomer InChIKey | DFZILPQHSXNRKO-UWAJQKTGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
FERULOYL_COA
CAFFEIC-ACID-COENZYME-A-THIOLESTER
(R-P)-[17-O,18-O]-URIDYLYL-3'->5'-ADENOSINE
5'-O-(URIDIN-3'-YLOXYTHIOPHOSPHORYL)ADENOSINE (DIASTEREOMER MIXTURE)
3'-O-[[BIS-(BENZYLOXY)-PHOSPHINYL]-OXY]-2'-O-(4-METHOXYBENZYL)-5'-O-PHOSPHATE-ADENOSINE
N-(6)-BENZOYL-3'-O-[[BIS-(BENZYLOXY)-PHOSPHINYL]-OXY]-2'-O-(4-METHOXYBENZYL)-ADENOSINE
cyclic AMP, 3TMS
ADENOSINE-3',5'-CYCLOPHOSPHATE-2'-PHOSPHATE
3',5'-O-(TETRA-ISOPROPYL-DISILOXANE-1,3-DIYL)-N(6)-BENZOYL-ADENOSINE
| 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 |