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Conformationally constrained analogues of diacylglycerol. 19. Synthesis and protein kinase C binding affinity of diacylglycerol lactones bearing an N-hydroxylamide side chain.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2003 Jun 19; Vol. 46 (13), pp. 2790-3. - Publication Year :
- 2003
-
Abstract
- The structures of N-hydroxylamides 1a and 1b, previously reported by Lee et al. in J. Med. Chem. 2001, 44, 4309-4312 as strong protein kinase C (PK-C) ligands, were incorrect and correspond instead to esters 2a and 2b, respectively. Here, we report the synthesis and complete characterization of 1a and 1b together with the associated biological activity in terms of PK-C binding affinity.
- Subjects :
- 4-Butyrolactone analogs & derivatives
4-Butyrolactone chemistry
Diglycerides chemistry
Lactones chemistry
Ligands
Magnetic Resonance Spectroscopy
Molecular Conformation
Protein Binding
Stereoisomerism
Structure-Activity Relationship
4-Butyrolactone chemical synthesis
Diglycerides chemical synthesis
Lactones chemical synthesis
Protein Kinase C chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 46
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12801241
- Full Text :
- https://doi.org/10.1021/jm030082c