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Novel retinoidal tropolone derivatives. Bioisosteric relationship of tropolone ring with benzoic acid moiety in retinoid structure
- Source :
- Chemicalpharmaceutical bulletin. 49(4)
- Publication Year :
- 2001
-
Abstract
- Several tropolone derivatives (4-7) were designed as novel retinoids on the assumption that the tropolone ring may mimic the benzoic acid moiety in retinoid structures, such as Am80 (2). Among the synthesized compounds, 5-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)ethynyl]tropolone (7a) showed moderate potency as a differentiation-inducer of HL-60 cells. The activities of the tropolones were greatly enhanced in the presence of HX630, an RXR agonist (retinoid synergist).
- Subjects :
- Stereochemistry
medicine.drug_class
Receptors, Retinoic Acid
HL-60 Cells
Retinoid X receptor
Ring (chemistry)
Chemical synthesis
Benzoates
Tropolone
chemistry.chemical_compound
Retinoids
Isomerism
Drug Discovery
medicine
Moiety
Humans
Retinoid
Benzoic acid
Bicyclic molecule
Chemistry
Cell Differentiation
Drug Synergism
General Chemistry
General Medicine
Retinoid X Receptors
Transcription Factors
Subjects
Details
- ISSN :
- 00092363
- Volume :
- 49
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Chemicalpharmaceutical bulletin
- Accession number :
- edsair.doi.dedup.....a7f4f6d8c2d85db0044e4f88d0228f20