M. B. Martin

发表

Bisphosphonates Are Potent Inhibitors of Trypanosoma cruzi Farnesyl Pyrophosphate Synthase*

E. Oldfield, R. Docampo, Michael B. Martin, 2001, The Journal of Biological Chemistry.

Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: a potential route to chemotherapy.

E. Oldfield, V. Yardley, S. Croft, 2001, Journal of medicinal chemistry.

Effects of butylated hydroxyanisole on the aryl hydrocarbon hydroxylase of rats and mice.

C. S. Yang, M. B. Martin, K. Lewis, 1981, Chemico-biological interactions.

Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis.

R. D. Dyer, P. Young, J. Summers, 1988, Journal of medicinal chemistry.

Preparation of 4α,8β-dimethyl-4β-methoxycarbonyl-17a-oxa-D-homo-androstan-17-one, intermediate of interest in the synthesis of 8β-methyl-testolactone

M. B. Martin, R. Gonzalez, A. Mateos, 1989 .

Synthesis of 4-hydroxy-15-oxaandrost-4-en-3-one and other potential aromatase inhibitors from sandaracopimaric acid

M. B. Martin, R. Gonzalez, A. Mateos, 1995 .

Structure-activity relationships of N-hydroxyurea 5-lipoxygenase inhibitors.

R. Maki, P. Young, J. Summers, 1997, Journal of medicinal chemistry.

(31)P NMR of apicomplexans and the effects of risedronate on Cryptosporidium parvum growth.

E. Oldfield, S. Luo, R. Docampo, 2001, Biochemical and biophysical research communications.

Nitrogen-containing bisphosphonates as carbocation transition state analogs for isoprenoid biosynthesis.

E. Oldfield, J. Urbina, W. Arnold, 1999, Biochemical and biophysical research communications.