Results 111 to 120 of about 19,239 (193)
Selenium biofortification and phytoremediation phytotechnologies: A review [PDF]
Pilon-Smits, Elizabeth A. H.+1 more
core +1 more source
Dissociating Hydra Tissue into Single Cells ba the Maceration Technique [PDF]
David, Charles N., Lenhoff, Howard M.
core +1 more source
Unravelling the role of SNM1 in the DNA repair system of Trypanosoma brucei [PDF]
Ali, S+11 more
core +1 more source
New compounds: N-arylglyoxylohydroxamyl derivatives of nitrogen mustard
The synthesis and physical properties of some N,N - bis (2 - chloroethyl)arylglyoxylohy-droxamamides are described.
Joseph P. Larocca, C.A. Gibson
openaire +4 more sources
The rates of formation of ethyleneimonium ion resulting only from the initial cyclization of a β-chloroethyl group of various nitrogen mustard compounds are reported. A polarographic technique was used for the quantitative determination of the ethyleneimonium ions.
Adelbert M. Knevel+2 more
openaire +4 more sources
Phosphorus-nitrogen compounds. 24. Phosphoramide mustard carrier derivatives
AbstractDargestellt und auf Antitumor‐Aktivität untersucht werden die Verbindungen (I)‐(III).
van der Helm D+3 more
openaire +5 more sources
The Synthesis Of Nitrogen Mustard Derivatives Of Some Steroids And Related Compounds.
PhD ; Chemistry ; University of Michigan, Horace H. Rackham School of Graduate Studies ; http://deepblue.lib.umich.edu/bitstream/2027.42/179112/2/0003761 ...
George G. Hazen
openaire +3 more sources
The influence of some sulfur-containing compounds on the toxicity of nitrogen mustards
Abstract Measurements of the effect of nitrogen mustards on the cholinesterase activity of the small intestine of rats indicated that HN1 and HN2 cause a decrease in enzyme activity of the intestine that is maximal at 2–4 days after administration and is reversible after sublethal doses of the nitrogen mustards.
Hietbrink Be, Raymund Ab
openaire +4 more sources
Nitrogen mustard and radiogold in combination markedly inhibit growth of the intraperitoneal ascitic form of the Ehrlich ascites carcinoma in mice. The best inhibiting dose of radiogold, 15 mc/kg, was the most toxic one; 7.5 mc/kg was found to be the most effective dose with the least toxicity.
Raymond R. Lanier+2 more
openaire +4 more sources
16 heterocyclic nitrogen mustards (ICR compounds), which were synthesized for use as possible antitumor agents by Creech and coworkers, were tested for mutagenicity in Salmonella typhimurium strains TA1535, TA1536, TA1537, TA1538, TA98 and TA100. The compounds were incorporated into the top agar at 5 doses: 0.5, 1, 2.5, 5 and 10 micrograms/plate.
Alan J. Katz+3 more
openaire +4 more sources