benzimidazole

The benzimidazole is then alkylated with the desired 1-chloro-2-dialkylaminoethane, forming the final product.

It is the most potent benzimidazole opioid currently known.

A large number of related benzimidazole derived cannabinoid ligands are known.

A second treatment, again using a modern benzimidazole or ivermectin, is recommended 3-4 weeks later to remove any residual infection.

Commonly used bases are morpholine, 4-methylpyridine, imidazole and benzimidazole.

Hypersensitivity to the benzimidazole class of compounds.

The main focus of modification of timoprazole was the benzimidazole part of its structure.

The portion of the molecule common to all three compounds, the aromatic benzimidazole, is thus the most likely point of interaction for W89.

It is a dimethoxy-substituted pyridine bound to a fluoroalkoxy substituted benzimidazole.

Rabeprazole is a novel benzimidazole compound on market, since 1999 in USA.

They replaced the imidazopyridine with benzimidazole and the benzhydril group was swapped out for a benzamide.

Oxfendazole is the sulfoxide form of fenbendazole, a broad spectrum benzimidazole anthelmintic.

However, necessary intramolecular rearrangement of the benzimidazole into sulfenamide posed severe geometric constraints.

Differing pyridine and benzimidazole substituents result in small, but potentially significant different physical and chemical properties.

Carbendazim is a widely used, broad-spectrum benzimidazole fungicide and a metabolite of benomyl.

Our data does not support an interaction of this amino acid with either the N-benzyl or benzimidazole portions of lerisetron.

The drugs of choice for treatment and prevention of E. cuniculi infections are the benzimidazole anthelmintics, particularly fenbendazole.

The benzimidazole drugs share a common molecular structure, triclabendazole being the exception in having a chlorinated benzene ring but no carbamate group.

Addition of 5-methoxy-substitution to the benzimidazole moiety of omeprazole was also made and gave the compound much more stability at neutral pH.

Addition of a trifluoromethyl group to the benzimidazole moiety led to a series of very active compounds with varying solution-stability.

Research suggest that this is due to the strong coordination between benzimidazole and the central cobalt atom, pulling it down into the plane of corrin ring.

The drug of choice in the treatment of fasciolosis is triclabendazole, a member of the benzimidazole family of anthelmintics.

In the interaction of candesartan with AT receptor the carboxyl group of the benzimidazole ring plays an important role.

It is a systemic benzimidazole fungicide that is selectively toxic to microorganisms and invertebrates, especially earthworms.

It has a difluoroalkoxy sidegroup on the benzimidazole part and two methoxy groups in position 3 and 4 on the pyridine.