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1.
Comput Intell Neurosci ; 2022: 4951080, 2022.
Article in English | MEDLINE | ID: mdl-36035855

ABSTRACT

Based on Rusch's creep constitutive relation, differential equations for the redistribution of shrinkage internal force and creep of the composite beam are derived and solved. The closed solution is cumbersome and is inconvenient to be applied practically. It is hard to solve the accurate solution for coupled differential equations. Therefore, a simplified approach is given. However, it ignores the influence of the redistribution of bending moment of the concrete slab on the axial strain and removes the coupling relationship of differential equations so that it makes the solution become convenient. The comparison of the results calculated by the two approaches shows that their calculated errors are small, within 3%, when the stiffness ratio of the concrete slab and the steel beam are less than 0.185. It also shows that the greater the stiffness of the steel beam, the greater the constraint on the creep of the concrete slab, so is the redistribution of internal force.

2.
Pestic Biochem Physiol ; 164: 26-32, 2020 Mar.
Article in English | MEDLINE | ID: mdl-32284133

ABSTRACT

The phytopathogenic fungus Fusarium graminearum is the major causal agent of fusarium head blight (FHB), which is one of the most serious diseases in wheat. Based on our previous work, the 1,2,3-triazole phenylhydrazone scaffold was further optimized at three modification sites to improve its antifungal activity against F. graminearum. The optimization yielded compound 8d was discovered to be a potent fungicidal agent with an EC50 value of 0.28 µg/mL against F. graminearum, which is 3.6 times lower than previously reported. In addition, 8d also exhibited good inhibitory activities against Rhizoctonia solani and Sclerotinia sclerotiorum with EC50 values of 0.86 and 1.66 µg/mL, respectively. In vivo testing demonstrated that 8d could effectively suppress the disease development of FHB at 200 µg/mL with a protection efficacy of 80.6%. Scanning electron micrographs and transmission electron micrographs showed that the external morphology and internal contents of F. graminearum hyphae were abnormal after 24 h of 8d treatment. Therefore, compound 8d was a promising fungicide candidate for further development.


Subject(s)
Fungicides, Industrial , Fusarium , Hydrazones , Plant Diseases , Triazoles
3.
Pestic Biochem Physiol ; 156: 160-169, 2019 May.
Article in English | MEDLINE | ID: mdl-31027576

ABSTRACT

Succinate dehydrogenase (SDH) is demonstrably one of the most important molecular targets in development of new fungicide. In our continuous efforts to discover novel SDH inhibitors, forty-two carboxamide derivatives containing 1,2,3-triazole ring were designed and synthesized, which were precisely characterized by 1H NMR, ESI-MS, elemental analysis and X-ray single-crystal diffraction. The compounds were screened for antifungal activities against phytopathogenic fungi by mycelia growth inhibition assay in vitro. Compound A3-3 exhibited significant antifungal activity against Sclerotinia sclerotiorum, Botrytis cinerea, Rhizoctonia cerealis and Gaeumannomyces graminsis with EC50 values of 1.08, 8.75, 1.67 and 5.30 µg/mL, respectively, comparable to those of commercial SDHI boscalid. In vivo testing demonstrated that A3-3 was effective for suppressing rape sclerotinia rot, cucumber grey mould and wheat powdery mildew caused by S. sclerotiorum, B. cinerea and Blumeria graminis at a dosage of 200 µg/mL. Inhibition activities against SDH test proved the designed analogues were effective in the enzyme level. The molecular docking simulation revealed that A3-3 interacted with ARG43,TYR58 and TRP173 of the SDH through hydrogen bond and pi-pi interaction, which could explain the probable mechanism of action between the inhibitor and target protein.


Subject(s)
Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/pharmacology , Succinate Dehydrogenase/metabolism , Triazoles/chemistry , Enzyme Activation/drug effects , Molecular Docking Simulation , Molecular Structure , Structure-Activity Relationship
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