Results 151 to 160 of about 12,670 (192)

2-(Cyanomethyl)benzimidazole Derivatives as 1,3-Dicarbonyl Analogues for a Kinetically Controlled Diastereo- and Enantioselective Mannich-Type Reaction Catalyzed by Chiral Phosphoric Acid. [PDF]

Org Lett
Ye H, Hou L, Takeda A, Sato T, Yadav J, Kikuchi J, Bao M, Terada M.   +7 more
europepmc   +1 more source

Beyond fenbendazole: Molecular and integrated pathways for managing poultry ascarid resistance. [PDF]

Poult Sci
Rattanapitoon SK, Charoenphon N, Rattanapitoon NK.   +2 more
europepmc   +1 more source

Microbiological evidence for the trisubstituted benzimidazoles targeting MmpL3 in Mycobacterium tuberculosis. [PDF]

Antimicrob Agents Chemother
Zhang M, Zhang M, Allen R, Ames L, Engelhart CA, Quach D, Lv X, Xiao G, Wang H, Wang J, Zhou L, Pan M, Sugie J, Pogliano J, Schnappinger D, Parish T, Chen S.   +16 more
europepmc   +1 more source

Lethal effect of heterologous Haemonchus contortus α- and β-tubulin expression in Leishmania tarentolae. [PDF]

PLoS One
Borchert M, Krücken J, Müller M, von Samson-Himmelstjerna G.   +3 more
europepmc   +1 more source

Synthesis and SARs of benzimidazoles: insights into antimicrobial innovation (2018-2024). [PDF]

RSC Adv
Ibrahim AA, Said EG, AboulMagd AM, Amin NH, Abdel-Rahman HM.   +4 more
europepmc   +1 more source

Identification and biological evaluation of benzimidazole-based compounds as novel TGFβR1 inhibitors. [PDF]

J Enzyme Inhib Med Chem
Tseng HJ, Wu YW, Chen YL, Lin TE, Fang-Chin YT, Wu YL, Sung TY, Yen SC, Hsieh JH, Hsu KC, Pan SL.   +10 more
europepmc   +1 more source

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Poly(benzimidazole)

2009
Abstract Major Applications Fire-resistant material, replacement for asbestos, thermal-protective clothing, ion-exchange resins, microporous absorbent beads, membrane applications. Properties of Special Interest High-temperature stability, nonflammability, unusual resistance to organic solvents, excellent mechanical properties ...
Vladyslav Kholodovych, William J Welsh
openaire   +1 more source

Iron–sulphur dimers with benzimidazolate–thiolate, benzimidazolate–phenolate, or bis(benzimidazolate) terminal chelating ligands

J. Chem. Soc., Chem. Commun., 1986
[Fe2S2L2]2– complexes co-ordinated by the mixed-donor N–S, N–O, or N–N ligands L1–L4 are characterised by electronic and n.m.r. spectroscopy and shown to undergo one-electron reduction to the corresponding trianions with e.s.r. spectra exhibiting a range of g-tensor values which are compared with those for [2Fe–2S]+ proteins of the Rieske type.
Peter Beardwood, John F. Gibson
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Biochemistry of benzimidazole resistance

Acta Tropica, 1994
Heavy reliance on the benzimidazole (BZ) anthelmintics since their introduction in the 1960's for the control of gastrointestinal parasites of livestock has led to widespread BZ resistance in target parasite species. The BZs exert their primary action by binding to tubulin, the major protein component of microtubules.
E, Lacey, J H, Gill
openaire   +2 more sources

Benzimidazole Ligands

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
openaire   +1 more source