James A. Fishback

发表

New positron emission tomography (PET) radioligand for imaging σ-1 receptors in living subjects.

S. Gambhir, C. H. Nielsen, M. James, 2012, Journal of medicinal chemistry.

Conversion of a highly selective sigma-1 receptor-ligand to sigma-2 receptor preferring ligands with anticocaine activity.

J. Poupaert, Yan-tong Xu, Nidhi Kaushal, 2008, Journal of medicinal chemistry.

Structure activity relationship study of benzo[d]thiazol-2(3H)one based σ receptor ligands.

J. Poupaert, C. McCurdy, James A. Fishback, 2013, Bioorganic & medicinal chemistry letters.

A 96-well filtration method for radioligand binding analysis of σ receptor ligands.

C. McCurdy, James A. Fishback, R. Matsumoto, 2012, Journal of pharmaceutical and biomedical analysis.

New methodologies for in vitro analysis of binding and functional activity of sigma receptor ligands

James A. Fishback, 2011 .

Noribogaine is a G-protein biased κ-opioid receptor agonist

D. Mash, S. Schürer, Emeline L. Maillet, 2015, Neuropharmacology.

A Novel Oligodeoxynucleotide Inhibitor of Thrombin. II. Pharmacokinetics in the Cynomolgus Monkey

William A. Lee, J. Shaw, L. C. Bock, 1995, Pharmaceutical Research.

Sigma receptors: potential targets for a new class of antidepressant drug.

Yan-tong Xu, James A. Fishback, R. Matsumoto, 2010, Pharmacology & therapeutics.

Synthesis and characterization of [³H]-SN56, a novel radioligand for the σ₁ receptor.

J. Poupaert, C. McCurdy, C. Mesangeau, 2011, European journal of pharmacology.

Molecular and Cellular Pharmacology Synthesis and characterization of ( 3 H)-SN56, a novel radioligand for the σ1 receptor

J. Poupaert, C. McCurdy, C. Mesangeau, 2011 .

Oral Bioavailability of the Antiretroviral Agent 9-(2-phosphonylmethoxyethyl)adenine (PMEA) from Three Formulations of the Prodrug Bis(pivaloyloxymethyl)-PMEA in Fasted Male Cynomolgus Monkeys

William A. Lee, J. Shaw, K. Soike, 1994, Pharmaceutical Research.

Sodwanone and yardenone triterpenes from a South African species of the marine sponge Axinella inhibit hypoxia-inducible factor-1 (HIF-1) activation in both breast and prostate tumor cells.

D. Nagle, James A. Fishback, Yu-Dong Zhou, 2006, Journal of natural products.

Synthesis and opioid activity of enantiomeric N-substituted 2,3,4,4a,5,6,7,7a-octahydro-1H-benzofuro[3,2-e]isoquinolines.

R. Rothman, C. Dersch, James A. Fishback, 2010, Journal of medicinal chemistry.

Modified deoxyoligonucleotides stable to exonuclease degradation in serum.

J. Shaw, J. Shaw, K. Kent, 1991, Nucleic acids research.