L. Mcquaid

发表

LY191704: a selective, nonsteroidal inhibitor of human steroid 5 alpha-reductase type 1.

C. D. Jones, D. Russell, N. Stamm, 1993, Proceedings of the National Academy of Sciences of the United States of America.

LY191704 inhibits type I steroid 5 alpha-reductase in human scalp.

C. D. Jones, D. Tindall, B. Neubauer, 1996, The Journal of clinical endocrinology and metabolism.

Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid

P. Bartlett, L. Mcquaid, 1984 .

Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones.

P. Ornstein, D. Schoepp, D. Lodge, 1992, Journal of medicinal chemistry.

Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones.

P. Ornstein, D. Schoepp, D. Lodge, 1992, Journal of medicinal chemistry.

3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex.

D. Lodge, E. Pralong, J. Wikel, 1992, Journal of medicinal chemistry.

Substituted 5-amino-4,5,6,7-tetrahydroindazoles as partial ergoline structures with dopaminergic activity.

D. Wong, J. Clemens, R. Fuller, 1989, Journal of medicinal chemistry.

An enantioselective synthesis of D-(-)- and L-(+)-2-amino-3-phosphonopropanoic acid

E. C. Smith, J. Paschal, L. Mcquaid, 1990 .

Stereoselectivity and mode of inhibition of phosphoinositide-coupled excitatory amino acid receptors by 2-amino-3-phosphonopropionic acid.

D. Schoepp, B. Johnson, E. C. Smith, 1990, Molecular pharmacology.

LY 191704 : A selective , nonsteroidal inhibitor of human steroid 5 a-reductase type 1 ( 5 a-reductase / dihydrotestosterone / benzoquinolinone / benign prostatic hyperplasia )

C. D. Jones, D. Russell, N. Stamm, 2005 .

Nonsteroidal inhibitors of human type I steroid 5-alpha-reductase.

A. Pike, N. Stamm, B. Neubauer, 1993, Journal of medicinal chemistry.

5,7-Dichlorokynurenic acid, a potent and selective competitive antagonist of the glycine site on NMDA receptors

R. Dingledine, P. J. O'malley, E. C. Smith, 1990, Neuroscience Letters.

Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[ƒ]quinolinones derived from palladium mediated coupling reactions

B. Neubauer, J. Audia, V. P. Rocco, 1998 .

Synthesis and 5α‐Reductase Inhibitory Activity of 8‐Substituted Benzo[f]quinolinones Derived from Palladium Mediated Coupling Reactions.

B. Neubauer, J. Audia, E. C. Smith, 2010 .

QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase.

Charles David Jones, James H. Wikel, Kerry G. Bemis, 1993 .