piperazine

The most likely candidate is the other nitrogen of the piperazine ring.

Quipazine is a piperazine drug used in scientific research.

Piperazine was first introduced as an anthelmintic in 1953.

Piperazine and similar diamines also reduce the number of hydrogen bonds.

The final step involved a nucleophilic substitution of the 2-chloro group by piperazine at high temperatures.

Acepromazine should not be used in horses dewormed with piperazine.

A large number of piperazine compounds have anthelmintic action.

Many currently notable drugs contain a piperazine ring as part of their molecular structure.

Y152 is shown positioned between the two piperazine nitrogens.

These results suggest a partial interaction of Y152 with the distal piperazine nitrogen.

Thus Y152A may form a partial interaction with both piperazine nitrogens.

Serious effects on the heart may also occur from a zopiclone overdose when combined with piperazine.

This may cause migration of the worm into the esophagus, so it is usually combined with piperazine.

Side effects include headaches and nausea, similar to those of other recreationally-used piperazine derivatives.

It is a salt of estrone sulfate and piperazine.

Introducing this into a reaction with 1-(2-furoyl)piperazine gives prazosin.

It belongs to the piperazine class of phenothiazines.

Physicians cleared the developing adults with a course of piperazine, effectively ending the infestation.

Research on ivermectin, piperazine, and dichlorvos in combinations also shows potential for toxicity.

Meclozine is a first-generation antihistamine of the piperazine class.

In the UK, mebendazole and piperazine are currently (2007) preferred.

Nefazadone is a piperazine compound incorporating a 1,2,4-triazol-3-one ring.

These data support our hypothesis that Y142 interacts with the distal piperazine nitrogen of lerisetron.

Y142 is shown interacting with the distal piperazine nitrogen possibly through a cation-π interaction.

Its chemical structure contains a piperazine ring.