Coumarinylmethyl Esters for Ultrafast Release of High Concentrations of Cyclic Nucleotides upon One‐ and Two‐Photon Photolysis
- 8 December 2005
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (48) , 7887-7891
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Kinetics Study of the Photocleavage of (Coumarin-4-yl)methyl EstersThe Journal of Physical Chemistry A, 2005
- Control of Cellular Activity2005
- Bhc‐cNMPs as either Water‐Soluble or Membrane‐Permeant Photoreleasable Cyclic Nucleotides for both One‐ and Two‐Photon ExcitationChemBioChem, 2004
- [3] New caged groups: 7-substituted coumarinylmethyl phosphate esters2004
- [7‐(Dialkylamino)coumarin‐4‐yl]methyl‐Caged Compounds as Ultrafast and Effective Long‐Wavelength Phototriggers of 8Bromo‐Substituted Cyclic NucleotidesChemBioChem, 2003
- Photolabile Precursors of Cyclic Nucleotides with High Aqueous Solubility and StabilityThe Journal of Organic Chemistry, 2002
- Langwellig UV/Vis-anregbare, hocheffiziente und ultraschnelle Phototrigger für cAMP und cGMPAngewandte Chemie, 2001
- Synthesis, photochemistry and application of (7-methoxycoumarin-4-yl)methyl-caged 8-bromoadenosine cyclic 3′,5′-monophosphate and 8-bromoguanosine cyclic 3′,5′-monophosphate photolyzed in the nanosecond time regionJournal of Photochemistry and Photobiology B: Biology, 1999
- Synthesis and reactivity of guanosine 3′,5′-phosphoric acid alkyl estersBioorganic Chemistry, 1979
- Synthesis, structure, and reactivity of adenosine cyclic 3',5'-phosphate-benzyltriestersJournal of Medicinal Chemistry, 1977