Results 41 to 50 of about 20,000 (189)

4-(Nitrophenylsulfonyl)piperazines mitigate radiation damage to multiple tissues. [PDF]

open access: yesPLoS ONE, 2017
Our ability to use ionizing radiation as an energy source, as a therapeutic agent, and, unfortunately, as a weapon, has evolved tremendously over the past 120 years, yet our tool box to handle the consequences of accidental and unwanted radiation ...
Ewa D Micewicz   +17 more
doaj   +1 more source

Piperazine-2,3,5,6-tetraone [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
The mol-ecule of the title compound, C(4)H(2)N(2)O(4), is located around an inversion center and the four O atoms are in the 2,3,5,6-positions of the piperazine ring. In the crystal, bifurcated N-H⋯O hydrogen bonds link the mol-ecules into a corrugated layer parallel to (101).
Jing-Jing Jia   +4 more
openaire   +4 more sources

Piperazine Abuse and Psychosis: A Systematic Review of the Literature

open access: yesPsychiatry International
Background: Piperazines, synthetic compounds known for their stimulant and hallucinogenic effects, have gained prominence among novel psychoactive substances (NPS) and are frequently associated with adverse psychiatric outcomes, including psychosis ...
Alessio Mosca   +9 more
doaj   +1 more source

Synthesis and Antimicrobial Activity of Some Novel Substituted Piperazinyl-quinazolin-3(4H)-ones

open access: yesE-Journal of Chemistry, 2008
Several substituted-quinazolin-3(4H)-ones were synthesized by condensation of 2-chloro-N-(4-oxo-substituted-quinazolin-3(4H)-yl)-acetamides with various substituted piperazines through single step reaction. Elemental analysis, IR, 1HNMR and mass spectral
N. M. Raghavendra   +2 more
doaj   +1 more source

Einiges über Piperazin [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1891
n ...
Schmidt, Albr, Wichmann, G.
openaire   +2 more sources

Designer drugs: aspectos analíticos e biológicos

open access: yesQuímica Nova, 2012
In the recent years, analytical toxicologists have been facing difficulties in detecting designer drugs due to the chemical modifications on the existing structures and the speed in which they are released into the market, requiring the development and ...
Rachel Bulcão   +7 more
doaj   +1 more source

Complexation of Constrained Ligands Piperazine, N-substituted Piperazines, and Thiomorpholine

open access: yesAustralian Journal of Chemistry, 2009
Complexation of the symmetric cyclic diamine piperazine (1,4-diazacyclohexane) has been examined in dry dimethyl formamide by spectrophotometric titrations (with Cu2+, Ni2+) to define formation constants, and by stopped-flow kinetics to define the complexation rates and reaction pathway.
Clifford, Sarah E.   +8 more
openaire   +2 more sources

Investigation of piperazines as human carbonic anhydrase I, II, IV and VII activators

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2018
Four human (h) carbonic anhydrase isoforms (CA, EC 4.2.1.1), hCA I, II, IV, and VII, were investigated for their activation profile with piperazines belonging to various classes, such as N-aryl-, N-alkyl-, N-acyl-piperazines as well as 2,4-disubstituted ...
Andrea Angeli   +4 more
doaj   +1 more source

Simplified Procedure for General Synthesis of Monosubstituted Piperazines—From a Batch Reaction Vessel to a Flow (Microwave) Reactor

open access: yesMolecules, 2020
We reported a novel simplified synthetic procedure for the preparation of monosubstituted piperazine derivatives which can now be easily prepared in a one-pot-one-step way from a protonated piperazine with no need of introduction of a protecting group ...
Dana Němečková   +4 more
doaj   +1 more source

Iridium-Catalyzed Asymmetric Ring-Opening of Oxabenzonorbornadienes with N-Substituted Piperazine Nucleophiles

open access: yesMolecules, 2015
Iridium-catalyzed asymmetric ring-opening of oxabenzonorbornadienes with N-substituted piperazines was described. The reaction afforded the corresponding ring-opening products in high yields and moderate enantioselectivities in the presence of 2.5 mol % [
Wen Yang, Renshi Luo, Dingqiao Yang
doaj   +1 more source

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