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Synthesis of 'neoprofen', a rigidified analogue of ibuprofen, exemplifying synthetic methodology for altering the 3-D topology of pharmaceutical substances
- Source :
- Organic & Biomolecular Chemistry. 14:7855-7858
- Publication Year :
- 2016
- Publisher :
- Royal Society of Chemistry (RSC), 2016.
-
Abstract
- 3,3-Dimethylcyclopentanes (neopentylenes) are ubiquitous in Nature but largely absent from synthetic pharmaceutical libraries. Neopentylenes define a hydrophobic and rigid 3-D topology with distinct molecular pharmacology, as exemplified here with two neopentylene-fused analogues of the synthetic anti-inflammatory drug, ibuprofen.
- Subjects :
- Drug
media_common.quotation_subject
Ibuprofen
010402 general chemistry
Topology
01 natural sciences
Biochemistry
Article
medicine
Humans
Physical and Theoretical Chemistry
Topology (chemistry)
media_common
Cyclooxygenase 2 Inhibitors
Molecular Structure
010405 organic chemistry
Chemistry
Anti-Inflammatory Agents, Non-Steroidal
Organic Chemistry
Molecular Pharmacology
Combinatorial chemistry
0104 chemical sciences
Cyclooxygenase 2
Pharmaceutical Substances
medicine.drug
Subjects
Details
- ISSN :
- 14770539 and 14770520
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Organic & Biomolecular Chemistry
- Accession number :
- edsair.doi.dedup.....f9554651b54008f6273812e433791e1e
- Full Text :
- https://doi.org/10.1039/c6ob01351a