<p>(a) Absorption spectrophotometric titration vs. pH of the free L<sup>2</sup> ligand; (b) electronic spectra of the protonated species of L<sup>2</sup>; (c) concentration distribution curves for the L<sup>2</sup> species. (I = 0.1 M (KCl) in 80% (w/w) MeOH/H<sub>2</sub>O; T = 25.0°C; [L<sup>2</sup>] = 5x10<sup>-5</sup>M; pH 1.6–11.02).</p
The achievements of modern domestic pharmacy clearly prove the prospects of searching for biological...
Piperine, the bioactive phytochemical from black pepper (Piper nigrum L.), is a nontoxic natural com...
Fyn tyrosine kinase inhibitors are considered potential therapeutic agents for a variety of human ca...
<div><p>A new class of TSCs containing piperazine (piperazinylogs) of Triapine, was designed to fulf...
A new class of TSCs containing piperazine (piperazinylogs) of Triapine, was designed to fulfill the ...
α-N-Heterocyclic thiosemicarbazones are among the most promising ribonucleotide reductase inhibitors...
Triapine is a novel inhibitor of ribonucleotide reductase (RR). It can remove ferric ion from the ca...
We present a comprehensive study of a water-soluble substance from the class of triazine derivatives...
The piperazine derivatives have been shown to inhibit human acetylcholinesterase. Virtual screening ...
The piperazine derivatives have been shown to inhibit human acetylcholinesterase. Virtual screening ...
<p>Individual IC50 values IC50 < 1μM, IC50 1–10 μM, IC50 > 10 μM are coded by red, yellow and grey, ...
Taking into account that multidrug resistance (MDR) is the main cause for chemotherapeutic failure i...
Five piperazine derivatives (S)-4-benzyl-1-(4-bromo-3-methylphenyl)-2 methylpiperazine (A), (S)-1-be...
The inhibition of the PD-1/PD-L1 axis by monoclonal antibodies has achieved remarkable success in tr...
Five piperazine derivatives (S)-4-benzyl-1-(4-bromo-3-methylphenyl)-2 methylpiperazine (A), (S)-1-be...
The achievements of modern domestic pharmacy clearly prove the prospects of searching for biological...
Piperine, the bioactive phytochemical from black pepper (Piper nigrum L.), is a nontoxic natural com...
Fyn tyrosine kinase inhibitors are considered potential therapeutic agents for a variety of human ca...
<div><p>A new class of TSCs containing piperazine (piperazinylogs) of Triapine, was designed to fulf...
A new class of TSCs containing piperazine (piperazinylogs) of Triapine, was designed to fulfill the ...
α-N-Heterocyclic thiosemicarbazones are among the most promising ribonucleotide reductase inhibitors...
Triapine is a novel inhibitor of ribonucleotide reductase (RR). It can remove ferric ion from the ca...
We present a comprehensive study of a water-soluble substance from the class of triazine derivatives...
The piperazine derivatives have been shown to inhibit human acetylcholinesterase. Virtual screening ...
The piperazine derivatives have been shown to inhibit human acetylcholinesterase. Virtual screening ...
<p>Individual IC50 values IC50 < 1μM, IC50 1–10 μM, IC50 > 10 μM are coded by red, yellow and grey, ...
Taking into account that multidrug resistance (MDR) is the main cause for chemotherapeutic failure i...
Five piperazine derivatives (S)-4-benzyl-1-(4-bromo-3-methylphenyl)-2 methylpiperazine (A), (S)-1-be...
The inhibition of the PD-1/PD-L1 axis by monoclonal antibodies has achieved remarkable success in tr...
Five piperazine derivatives (S)-4-benzyl-1-(4-bromo-3-methylphenyl)-2 methylpiperazine (A), (S)-1-be...
The achievements of modern domestic pharmacy clearly prove the prospects of searching for biological...
Piperine, the bioactive phytochemical from black pepper (Piper nigrum L.), is a nontoxic natural com...
Fyn tyrosine kinase inhibitors are considered potential therapeutic agents for a variety of human ca...