J. Gourvest

Biphenyls as surrogates of the steroidal backbone. Part 2: discovery of a novel family of non-steroidal 5-alpha-reductase inhibitors.

G. Teutsch, D. Lesuisse, E. Albert, 2001, Bioorganic & Medicinal Chemistry Letters.

Design and synthesis of potent and selective peptidomimetic Vitronectin receptor antagonists

T. Gadek, P. Broto, G. Breipohl, 2002 .

αvβ3 antagonists based on a central thiophene scaffold

S. Bodary, T. Gadek, J. Ruxer, 2001 .

RU54115, a tight-binding aromatase inhibitor potentially useful for the treatment of breast cancer

D. Lesuisse, B. Tric, J. Gourvest, 1992, The Journal of Steroid Biochemistry and Molecular Biology.

Determination of oenothein B as the active 5-alpha-reductase-inhibiting principle of the folk medicine Epilobium parviflorum.

G. Teutsch, M. Lowinski, P. Devaux, 1996, Journal of natural products.

RGD Mimetics containing a central hydantoin scaffold: αVβ3 vs αIIbβ3 selectivity requirements

S. Bodary, T. Gadek, J. Ruxer, 2000 .

Biphenyls as Surrogates of the Steroidal Backbone. Part 2. Discovery of a Novel Family of Non‐steroidal 5‐α‐Reductase Inhibitors.

G. Teutsch, D. Lesuisse, E. Albert, 2001 .