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Synthesis of diacetoxy acetal derivatives of santonin and their enhancing effects on HL-60 leukemia cell differentiation
- Source :
- Archives of Pharmacal Research. 29:40-45
- Publication Year :
- 2006
- Publisher :
- Springer Science and Business Media LLC, 2006.
-
Abstract
- Several diacetoxy acetal analogues have been synthesized from santonin and assessed for their ability of inducing or enhancing the differentiation of human HL-60 leukemia cells. The compounds themselves had little effect on HL-60 cell differentiation. However, three analogues, 2a, 3a, and 5b, synergistically enhanced 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3]-induced HL-60 cell differentiation when combined with 5 nM of dihydroxyvitamin D3 [1,25-(OH)2D3], a well-known differentiation inducer. Especially, the compound 5b profoundly enhanced the 1,25-(OH)2D3]-induced HL-60 cell differentiation.
- Subjects :
- Magnetic Resonance Spectroscopy
Stereochemistry
Cellular differentiation
Pharmacology toxicology
HL-60 Cells
Drug synergism
chemistry.chemical_compound
Calcitriol
Drug Discovery
medicine
Humans
Santonin
Nitroblue Tetrazolium
Organic Chemistry
Acetal
Cell Differentiation
Drug Synergism
Vitamins
Nuclear magnetic resonance spectroscopy
medicine.disease
Leukemia
chemistry
Molecular Medicine
Indicators and Reagents
Differentiation Inducer
Subjects
Details
- ISSN :
- 19763786 and 02536269
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Archives of Pharmacal Research
- Accession number :
- edsair.doi.dedup.....6a5c65ff86041523495c441ffcb0723c