Rosickyite-Benzimidazole and novantisol were ideal anthelmintic.
理想的驱虫药物有丙硫苯咪唑和左咪唑。
And a super high contrast was obtained when 6 nitro benzimidazole and thiosalicylic acid were used together.
而硫代水杨酸与6硝基苯并咪唑配合使用时，得到了超高反差效果。
New benzimidazole molecules with excellent corrosion inhibition properties were designed by 3d-qsar contour maps.
通过3d - QSAR等势图设计出了几种具有较好缓蚀性能的苯并咪唑化合物。
The present invention consists of ulcer activeness resisting benzimidazole compound and water soluble amide medicinal composite.
本发明包括含有具有抗溃疡活性的苯并咪唑化合物和水溶性酰胺的药用组合物。
Preferred transition metal compounds are based on cobalt and chromium, especially complexes thereof having benzimidazole ligands.
优选的过渡金属化合物基于钴和铬，尤其是其具有苯并咪唑配位体的络合物。
Benzimidazole and their derivatives are important material and intermediate product, it is a important structure cell which consist in many medicines.
苯并咪唑及其衍生物是有机合成中重要的原料和中间体，是一种存在于多种药物中的重要结构单元。
Aim to design and synthesize the novel aniline-type derivatives of benzimidazole, and to assay their activities of inhibiting secretion of gastric juice and gastric acids.
目的设计合成新型苯胺类苯并咪唑衍生物，并评价其对大白鼠胃液分泌和胃酸分泌的作用。
The invention provides an organic luminescent material, i. e. a terphenyl bridged-bis-benzimidazole quaternary ammonium compound, a preparation method and application thereof.
本发明提供一种三联苯桥联双苯并咪唑季铵盐类化合物有机发光材料、制备方法及应用。
The development of the benzimidazole and it's derivatives, especially two replacements of benzimidazole, is regarded as a category with a variety bioactivities of heterocyclic.
苯并咪唑及其衍生物的开发，尤其是二取代化合物越来越受到重视，被认为是一类具有多种生物生理活性的杂环。
In accordance with said invention, the ulcer activeness resisting water non-soluble benzimidazole compound can be solubilized and the stable medicinal composite can be provided.
按照本发明，可将具有抗溃疡活性的水不溶性苯并咪唑化合物增溶，并能提供稳定的药用组合物。
Benzopyran derivatives substituted with a benzimidazole derivative, pharmaceutically acceptable salts thereof, their preparations and pharmaceutical compositions containing them.
苯并咪唑衍生物取代的苯并吡喃衍生物，其药用盐，它们的制备方法和含有它们的药物组合物。
In the article, we dissertated comprehensively the functional mechanism, the relationship of structure, the synthetical methods and the safety of acylureas and the benzimidazole.
本文比较全面的论述了酰基脲化合物的作用机制、构效关系、合成方法和安全性以及苯并咪唑类化合物作用机制、安全性和应用情况。
The claimed invention provides benzimidazole derivatives antagonists of VR1, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
本发明披露作为VR1拮抗剂的苯并咪唑衍生物，制备它们的方法，含有它们的组合物和它们在治疗中的用途。
The present invention belongs to the field of medicine preparation, in the concrete, it relates to a composition of substituted benzimidazole proton pump inhibitor and its preparation method.
本发明涉及药物制剂领域，具体涉及含取代苯并咪唑质子泵抑制剂的组合物及其制备方法。
The present invention belongs to the field of medicine preparation, in the concrete, it relates to a composition of substituted benzimidazole proton pump inhibitor and its preparation method.
本发明涉及药物制剂领域，具体涉及含取代苯并咪唑质子泵抑制剂的组合物及其制备方法。
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