Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M. R. Rhodes"'
Autor:
R. E. Cotter, Robert N. McBurney, Eckard Weber, Kyle R. Gee, N. L. Reddy, John F. W. Keana, L.‐Y. Hu, M. R. Rhodes, P. Barmettler, P N Hamilton
Publikováno v:
Journal of Medicinal Chemistry. 36:1938-1946
IDDC (3, 10,5-(iminomethano)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene++ +) and a series of substituted derivatives were synthesized and evaluated in vitro for their ability to displace tritiated MK-801 ([3H]-2) from its specific binding site in guin
Autor:
John F. W. Keana, K. J. Burke‐Howie, James B. Fischer, Eckard Weber, M. R. Rhodes, N. L. Reddy, P. Barmettler
Publikováno v:
ChemInform. 25
Autor:
G R, Pettit, M R, Rhodes, D L, Herald, D J, Chaplin, M R, Stratford, E, Hamel, R K, Pettit, J C, Chapuis, D, Oliva
Publikováno v:
Anti-cancer drug design. 13(8)
The (E)-stilbene isomer (2a) of the (Z)-combretastatin A-4 prodrug (1b) was efficiently prepared from (E)-combretastatin A-4 by a reaction sequence employing phosphorylation (dibenzyl chlorophosphite), cleavage (trimethyliodosilane) of the benzyl est
Publikováno v:
Journal of natural products. 62(3)
Solution-phase synthesis of the marine sponge constituent phakellistatin 2 (1), cyclo(Tyr-Pro-Phe-Pro-Ile-Ile-Pro), was completed using a combination of stepwise coupling and (4 + 3) segment condensation. Use of diethyl phosphorocyanidate for the pep
Autor:
G R, Pettit, M R, Rhodes
Publikováno v:
Anti-cancer drug design. 13(3)
Combretastatin A-4 (1) as the phosphate ester prodrug (3d) is a potent antineoplastic and antiangiogenesis substance and is in advanced preclinical development. For the purpose of improving the phosphorylation synthetic sequence from combretastatin A
Autor:
M R, Rhodes, M, Rhodes
Publikováno v:
Pennsylvania medicine. 93(9)
This article combines the researched sciences of logic, philosophy, and medicine to develop a perspective on safety belt laws. The positions of advocacy and opposition are examined primarily by a nonphysician in a reasonably unbiased manner. The resu
Publikováno v:
ChemInform. 18