M. Lindstrom

发表

Discovery of potent, selective, and metabolically stable 4-(pyridin-3-yl)cinnolines as novel phosphodiesterase 10A (PDE10A) inhibitors.

E. Hu, R. Kunz, Shannon Rumfelt, 2012, Bioorganic & medicinal chemistry letters.

Discovery of a novel melanin concentrating hormone receptor 1 (MCHR1) antagonist with reduced hERG inhibition.

M. Lindstrom, J. Jaén, K. Dai, 2012, Bioorganic & medicinal chemistry letters.

T0070907, a Selective Ligand for Peroxisome Proliferator-activated Receptor γ, Functions as an Antagonist of Biochemical and Cellular Activities*

Yang Li, M. Lindstrom, P. Cao, 2002, The Journal of Biological Chemistry.

Regional expression and dietary regulation of rat small intestinal peptide and amino acid transporter mRNAs.

M. Lindstrom, J. Gum, Y. S. Kim, 1995, Biochemical and biophysical research communications.

Discovery of a new class of ghrelin receptor antagonists.

M. Lindstrom, Liang Tang, M. Lizarzaburu, 2012, Bioorganic & medicinal chemistry letters.

INT131: a selective modulator of PPAR gamma.

M. Lindstrom, N. Walker, Zhulun Wang, 2009, Journal of molecular biology.

Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.

M. Lindstrom, Zhulun Wang, Xiaoshan Min, 2011, Bioorganic & medicinal chemistry letters.

Co‐inhibition of immunoproteasome subunits LMP2 and LMP7 is required to block autoimmunity

J. M. Bradshaw, M. Lindstrom, M. Groettrup, 2018, EMBO reports.

Discovery and characterization of a potent and selective antagonist of melanin-concentrating hormone receptor 2.

M. Lindstrom, J. Jaén, Q. Ye, 2012, Bioorganic & medicinal chemistry letters.

T2384, a Novel Antidiabetic Agent with Unique Peroxisome Proliferator-activated Receptor γ Binding Properties*

M. Lindstrom, Xiaohong Liu, N. Walker, 2008, Journal of Biological Chemistry.

INT131: A Selective Modulator of PPARγ

M. Lindstrom, N. Walker, Zhulun Wang, 2009 .

Discovery and molecular basis of potent noncovalent inhibitors of fatty acid amide hydrolase (FAAH)

Zhihua Ma, Frank Kayser, Timothy J Carlson, 2011, Proceedings of the National Academy of Sciences.

Use of structure based design to increase selectivity of pyridyl-cinnoline phosphodiesterase 10A (PDE10A) inhibitors against phosphodiesterase 3 (PDE3).

E. Hu, R. Kunz, Shannon Rumfelt, 2012, Bioorganic & medicinal chemistry letters.

Discovery of INT131: a selective PPARγ modulator that enhances insulin sensitivity.

M. Lindstrom, N. Walker, P. Timmermans, 2013, Bioorganic & medicinal chemistry.

Identification of piperazine-bisamide GHSR antagonists for the treatment of obesity.

M. Lindstrom, M. Lizarzaburu, Ji Ma, 2010, Bioorganic & medicinal chemistry letters.