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Abstract
The design of a range of 4-position-modified D-myo-inositol 1,4,5-trisphosphate derivatives is described. The enantioselective synthesis of these compounds is reported, along with initial biological analysis, which indicates that these compounds do not act as D-myo-inositol 1,4,5-trisphosphate receptor agonists or antagonists.
Original language | English |
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Pages (from-to) | 5647-5659 |
Number of pages | 13 |
Journal | The Journal of Organic Chemistry |
Volume | 72 |
Issue number | 15 |
Early online date | 22 Jun 2007 |
DOIs | |
Publication status | Published - 20 Jul 2007 |
Keywords
- 2-AMINOETHOXYDIPHENYL BORATE 2-APB
- ADENOPHOSTIN-A
- MYOINOSITOL 1,4,5-TRISPHOSPHATE
- TRISPHOSPHATE RECEPTORS
- XESTOSPONGIN-C
- PENICILLIUM-BREVICOMPACTUM
- EXPEDITIOUS ROUTE
- POTENT INHIBITOR
- CALCIUM-RELEASE
- CA2+ PUMPS
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Dive into the research topics of 'The synthesis and biological action of novel 4-position-modified derivatives of D-myo-inositol 1,4,5-trisphosphate'. Together they form a unique fingerprint.Projects
- 1 Finished
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BB/C515255/1: A Reverse chemical genetics and chemical biology approach to probing 1,4,5-trisphosphate receptor function
Conway, S. J. (PI)
1/02/05 → 31/08/08
Project: Standard