Results 101 to 110 of about 33,790 (273)
Mechanism of Action of the Fungicide Thiabendazole, 2-(4′-Thiazolyl) Benzimidazole [PDF]
Paris M. Allen, David Gottlieb
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Fluorescence Spectra of Some Benzimidazoles in Acid Media [PDF]
Michio Kondo, Harumitsu Kuwano
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Reactivity of δ‐Functionalized para‐Quinone Methides in Nucleophilic Addition Reactions
The electrophilic reactivities of para‐quinone methides (pQMs) with functional groups at the exocyclic polarized carbon‐carbon double bond were determined by photometrical monitoring the kinetics of their reactions with carbanions in DMSO at 20°C. The experimental second‐order rate constants k2 were evaluated by the Mayr‐Patz equation, that is, the ...
Christoph Gross+3 more
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Polymerization of Ethylene Catalyzed by Vanadium(III) Complexes
Thirty five complexes of 1,2- bis(benzimidazole, benzothiazole and benzoxazole)benzene, 1,2-bis(benzimidazole, benzothiazole and benzoxazole)-4-methyl-benzene, 1,2-bis (benzimidazole, benzothiazole and benzoxazole)4-bromobenzene, 1, 2-bis ...
Hamdi Ali Elagab
doaj
Inhibition of Enterovirus Cytopathic Effects by 2-(α-Hydroxybenzyl)-Benzimidazole [PDF]
Rostom Bablanian+2 more
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Five CT cocrystals using TFBQ and fused, polycyclic donors derived from fluorene are synthesized. The π‐stacking in all cocrystals provides a platform for the displaying of in‐plane molecular motions of TFBQ, which is by supramolecular interactions.
Armando Navarro‐Huerta+7 more
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SPECTRUM AND CHARACTERISTICS OF THE VIRUS INHIBITORY ACTION OF 2-(α-HYDROXYBENZYL)-BENZIMIDAZOLE [PDF]
Hans J. Eggers, Igor Tamm
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Is Mycobacterial InhA a Suitable Target for Rational Drug Design?
InhA is the target of isoniazid, a first‐line antituberculosis drug. Isoniazid is, in fact, a prodrug that needs to be activated. Researchers are trying to develop direct inhibitors of InhA. This includes the resolution of crystallographic structures. The Protein Data Bank contains over a hundred InhA structures.
Julien Rizet+7 more
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BENZIMIDAZOLE: AN OVERVIEW [PDF]
Prabhat Kumar Upadhyaya+4 more
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CXCR4 is a transmembrane receptor overexpressed in a large variety of cancer cells. In addition to classical antibody‐ and peptide‐targeting for the development of Positron Emission Tomography (PET) radiopharmaceuticals, this receptor possesses a range of small organic inhibitors that can be exploited. These are based mainly on nitrogen‐rich scaffolds,
Marie M Le Roy+5 more
wiley +1 more source