S. Ghirmai

发表

Inhibition of serotonin and norepinephrine reuptake and inhibition of phosphodiesterase by multi-target inhibitors as potential agents for depression.

J. Cashman, S. Ghirmai, 2009, Bioorganic & medicinal chemistry.

Synthesis and pharmacological evaluation of 6-naltrexamine analogs for alcohol cessation.

J. Cashman, S. Ghirmai, M. Azar, 2009, Bioorganic & medicinal chemistry.

Synthesis and radioiodination of some daunorubicin and doxorubicin derivatives.

V. Tolmachev, E. Mume, S. Sjöberg, 2005, Carbohydrate research.

Enantioselective synthesis of m-carboranylalanine, a boron-rich analogue of phenylalanine

S. Sjöberg, S. Ghirmai, Charlotta G. M. Naeslund, 2005 .

Curcuminoids Inhibit Multiple Human Cytochromes P450, UDP-Glucuronosyltransferase, and Sulfotransferase Enzymes, whereas Piperine Is a Relatively Selective CYP3A4 Inhibitor

J. Cashman, M. Court, L. Volak, 2008, Drug Metabolism and Disposition.

Synthesis and radioiodination of some 9-aminoacridine derivatives for potential use in radionuclide therapy

H. Lundqvist, V. Tolmachev, E. Mume, 2005 .

Inhibition of Bfl-1 with N-aryl maleimides.

John Calvin Reed, J. Cashman, Brock T Brown, 2010, Bioorganic & medicinal chemistry letters.

1alpha,25-dihydroxyvitamin D3 interacts with curcuminoids to stimulate amyloid-beta clearance by macrophages of Alzheimer's disease patients.

K. Abel, J. Cashman, M. Hewison, 2009, Journal of Alzheimer's disease : JAD.

Inhibition of kappa opioid receptors attenuated increased cocaine intake in rats with extended access to cocaine

G. Koob, J. Cashman, S. Wee, 2009, Psychopharmacology.

Curcuminoids inhibit multiple human cytochromes P450 (CYP), UDP-glucuronosyltransferase (UGT), and sulfotransferase (SULT) enzymes, while piperine is a relatively selective CYP3A4 inhibitor.

J. Cashman, M. Court, L. Volak, 2008 .

Synthesis of Organic Compounds for Nuclide Therapy

S. Ghirmai, 2004 .

Immune defects in Alzheimer's disease: new medications development

K. Abel, J. Cashman, John R Cashman, 2008, BMC Neuroscience.

Evaluation in vitro of synthetic curcumins as agents promoting monocytic gene expression related to β-amyloid clearance.

K. Abel, J. Cashman, M. Lanier, 2012, Chemical research in toxicology.

Curcumins Promote Monocytic Gene Expression Related to β-Amyloid and Superoxide Dismutase Clearance

K. Abel, J. Cashman, M. Lanier, 2011, Neurodegenerative Diseases.

An aminoacridine derivative for radionuclide therapy: DNA binding properties studied in a novel cell-free in vitro assay.

H. Lundqvist, B. Stenerlöw, P. Malmström, 2005, International journal of oncology.