Development of long-acting dopamine transporter ligands as potential cocaine-abuse therapeutic agents: chiral hydroxyl-containing derivatives of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine. 2002

Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
Laboratory of Medicinal Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

In our search for long-acting agents for the treatment of cocaine abuse, a series of optically pure hydroxylated derivatives of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine (1) and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine (2) (GBR 12909 and GBR 12935, respectively) were synthesized and evaluated in vitro and in vivo. The enantiomers of the 2-hydroxylated analogues displayed substantial enantioselectivity. The S enantiomers displayed higher dopamine transporter (DAT) affinity and the R enantiomers were found to interact at the serotonin transporter (SERT) with higher affinity. The two-carbon spacer between the hydroxyl group and the piperazine ring was essential for enantioselectivity, and the length of the alkyl chain between the phenyl group and the piperazine ring influenced binding affinity and selectivity for the DAT and SERT. Phenylethyl analogues had a higher binding affinity for the SERT and a weaker affinity and selectivity for the DAT than the corresponding phenylpropyl analogues. Thus, (S)-(+)-1-[4-[2-[bis(4-fluorophenyl)methoxy]ethyl]piperazinyl]-3-phenylpropan-2-ol (6) displayed the highest affinity to the DAT, and (S)-(+)-1-[4-[2-(diphenylmethoxy)ethyl]piperazinyl]-3-phenylpropan-2-ol (8) had the highest selectivity. The latter (8) is one of the most DAT selective ligands known. In accord with the in vitro data, 6 showed greater potency than 7 in elevating extracellular dopamine levels in a microdialysis assay and in inhibiting cocaine-maintained responding in rhesus monkeys.

UI MeSH Term Description Entries
D008024 Ligands A molecule that binds to another molecule, used especially to refer to a small molecule that binds specifically to a larger molecule, e.g., an antigen binding to an antibody, a hormone or neurotransmitter binding to a receptor, or a substrate or allosteric effector binding to an enzyme. Ligands are also molecules that donate or accept a pair of electrons to form a coordinate covalent bond with the central metal atom of a coordination complex. (From Dorland, 27th ed) Ligand
D008253 Macaca mulatta A species of the genus MACACA inhabiting India, China, and other parts of Asia. The species is used extensively in biomedical research and adapts very well to living with humans. Chinese Rhesus Macaques,Macaca mulatta lasiota,Monkey, Rhesus,Rhesus Monkey,Rhesus Macaque,Chinese Rhesus Macaque,Macaca mulatta lasiotas,Macaque, Rhesus,Rhesus Macaque, Chinese,Rhesus Macaques,Rhesus Macaques, Chinese,Rhesus Monkeys
D008297 Male Males
D008562 Membrane Glycoproteins Glycoproteins found on the membrane or surface of cells. Cell Surface Glycoproteins,Surface Glycoproteins,Cell Surface Glycoprotein,Membrane Glycoprotein,Surface Glycoprotein,Glycoprotein, Cell Surface,Glycoprotein, Membrane,Glycoprotein, Surface,Glycoproteins, Cell Surface,Glycoproteins, Membrane,Glycoproteins, Surface,Surface Glycoprotein, Cell,Surface Glycoproteins, Cell
D009419 Nerve Tissue Proteins Proteins, Nerve Tissue,Tissue Proteins, Nerve
D010879 Piperazines Compounds that are derived from PIPERAZINE.
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001522 Behavior, Animal The observable response an animal makes to any situation. Autotomy Animal,Animal Behavior,Animal Behaviors
D001559 Benzhydryl Compounds Compounds which contain the methyl radical substituted with two benzene rings. Permitted are any substituents, but ring fusion to any of the benzene rings is not allowed. Diphenylmethyl Compounds,Compounds, Benzhydryl,Compounds, Diphenylmethyl

Related Publications

Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
September 1999, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
September 2002, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
December 2008, Neurochemistry international,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
December 2000, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
February 1997, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
October 2005, The Journal of pharmacology and experimental therapeutics,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
September 2001, Drug metabolism and disposition: the biological fate of chemicals,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
November 1996, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
April 2003, Journal of medicinal chemistry,
Ling-Wei Hsin, and Christina M Dersch, and Michael H Baumann, and David Stafford, and John R Glowa, and Richard B Rothman, and Arthur E Jacobson, and Kenner C Rice
January 2000, Journal of medicinal chemistry,
Copied contents to your clipboard!