Marisa M. Westlin

发表

R-isomers of Arg-Gly-Asp (RGD) mimics as potent αvβ3 inhibitors

D. Griggs, J. Malecha, J. Collins, 2007 .

Discovery of +(2-{4-[2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethoxy]phenyl}-cyclopropyl)acetic acid as potent and selective alphavbeta3 inhibitor: design, synthesis, and optimization.

I. Khanna, M. A. Russell, T. E. Rogers, 2007, Bioorganic & medicinal chemistry.

Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective αvβ3 receptor antagonists

Sarah A. Norring, Hongwei Wu, I. Khanna, 2006 .

Synthesis of pyrazoles and isoxazoles as potent αvβ3 receptor antagonists

T. Penning, M. B. Finn, W. Westlin, 2006 .

Synthesis of cinnamic acids and related isosteres as potent and selective αvβ3 receptor antagonists

T. Penning, S. Docter, J. Malecha, 2004 .

Anti-metastatic properties of RGD-peptidomimetic agents S137 and S247

D. Griggs, S. Schroeter, S. Settle, 2004, Clinical & Experimental Metastasis.

VCC-1, a novel chemokine, promotes tumor growth.

R. Mazzarella, D. Griggs, R. Head, 2006, Biochemical and biophysical research communications.

Abstracts of 20th Annual ASENT Meeting

K. Blennow, M. Grundman, R. Guilbaud, 2018, Neurotherapeutics.

R-isomers of Arg-Gly-Asp (RGD) mimics as potent alphavbeta3 inhibitors.

D. Griggs, J. Collins, M. B. Finn, 2007, Bioorganic & medicinal chemistry.