C. Lugar

发表

Structure-activity relationships of selective estrogen receptor modulators: modifications to the 2-arylbenzothiophene core of raloxifene.

H W Cole, C. D. Jones, K. Matsumoto, 1997, Journal of medicinal chemistry.

Novel 3-aryl indoles as progesterone receptor antagonists for uterine fibroids.

A. Geiser, T. I. Richardson, J. Dodge, 2011, ACS medicinal chemistry letters.

Evaluation of the major metabolites of raloxifene as modulators of tissue selectivity

J. Dodge, L. Short, H. Bryant, 1997, The Journal of Steroid Biochemistry and Molecular Biology.

Benzopyrans are selective estrogen receptor beta agonists with novel activity in models of benign prostatic hyperplasia.

G. Durst, A. Boodhoo, T. I. Richardson, 2006, Journal of Medicinal Chemistry.

Synthesis and biological evaluation of an orally active ghrelin agonist that stimulates food consumption and adiposity in rats.

M. Clay, T. Lindstrom, J. Dodge, 2004, Bioorganic & medicinal chemistry letters.

Alcohol inversion of 17β-steroids

J. Dodge, C. Lugar, Jeffrey Alan Dodge, 1996 .

Solid-phase synthesis of unnatural amino acids using unactivated alkyl halides

William L. Scott, Martin J. O'Donnell, C. Lugar, 1997 .

Structure-activity studies of 6-substituted decahydroisoquinoline-3-carboxylic acid AMPA receptor antagonists. 2. Effects of distal acid bioisosteric substitution, absolute stereochemical preferences, and in vivo activity.

P. Ornstein, D. Schoepp, D. Lodge, 1996, Journal of medicinal chemistry.

Benzopyrans as selective estrogen receptor beta agonists (SERBAs). Part 2: structure-activity relationship studies on the benzopyran scaffold.

Yong Wang, T. I. Richardson, J. Dodge, 2007, Bioorganic & medicinal chemistry letters.

Structure-activity studies of 6-(tetrazolylalkyl)-substituted decahydroisoquinoline-3-carboxylic acid AMPA receptor antagonists. 1. Effects of stereochemistry, chain length, and chain substitution.

P. Ornstein, D. Schoepp, D. Lodge, 1996, Journal of medicinal chemistry.

Defining Target Engagement Required for Efficacy In Vivo at the Retinoic Acid Receptor-Related Orphan Receptor C2 (RORγt).

G. Durst, D. Clawson, R. Morphy, 2021, Journal of medicinal chemistry.

Synthesis and estrogen receptor binding affinities of the major human metabolites of raloxifene (LY139481)

J. Dodge, A. Glasebrook, C. Lugar, 1997 .