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Authors = Weimin Ding

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WEIMIN (82) , DING (685)

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Open AccessArticle Design, Development, and Performance Evaluation of a Trash-Board Moldboard Plow for the Interaction between Soil and Straw with Two Different Water Content Levels
Agronomy 2016, 6(2), 30; doi:10.3390/agronomy6020030
Received: 23 December 2015 / Revised: 28 April 2016 / Accepted: 2 May 2016 / Published: 6 May 2016
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Abstract
A two-year field study was conducted to investigate the performance of a lightweight trash-board moldboard plow (with and without a trash-board), as influenced by stubble height and water content. Both fields were measured for the performance of a trash-board moldboard plow when used
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A two-year field study was conducted to investigate the performance of a lightweight trash-board moldboard plow (with and without a trash-board), as influenced by stubble height and water content. Both fields were measured for the performance of a trash-board moldboard plow when used during the optimization of the plowing depth, the water content, and the reaction forces. The results showed that in the first year, when a trash-board was required, the results were significantly different. The fields had lower draft and reaction force in the soil with only stubble height, which was greater than that in the soil with dense straw for all water content levels. This was also observed in the second year for the whole depth. This study shows that the moldboard plow with a trash-board provided minimum draft and reaction forces with only straw and heavy straw. The results indicate that straw nearby shear significantly increased displacement for all treatments, with variance of straw nearby moldboard. Hence, the results verify that a trash-board continuously created large soil fragmentation with different water content. Straw labels create a position of straw which also allows for better results. It is important to install trash-boards with the moldboard plow for heavy straw incorporation. Full article
(This article belongs to the Special Issue Interactions between Plant Rhizosphere and Soil Organisms)
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Open AccessArticle A 3D QSAR Study of Betulinic Acid Derivatives as Anti-Tumor Agents Using Topomer CoMFA: Model Building Studies and Experimental Verification
Molecules 2013, 18(9), 10228-10241; doi:10.3390/molecules180910228
Received: 2 July 2013 / Revised: 13 August 2013 / Accepted: 13 August 2013 / Published: 22 August 2013
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Abstract
Betulinic acid (BA) is a natural product that exerts its cytotoxicity against various malignant carcinomas without side effects by triggering the mitochondrial pathway to apoptosis. Betulin (BE), the 28-hydroxyl analog of BA, is present in large amounts (up to 30% dry weight) in
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Betulinic acid (BA) is a natural product that exerts its cytotoxicity against various malignant carcinomas without side effects by triggering the mitochondrial pathway to apoptosis. Betulin (BE), the 28-hydroxyl analog of BA, is present in large amounts (up to 30% dry weight) in the outer bark of birch trees, and shares the same pentacyclic triterpenoid core as BA, yet exhibits no significant cytotoxicity. Topomer CoMFA studies were performed on 37 BA and BE derivatives and their in vitro anti-cancer activity results (reported as IC50 values) against HT29 human colon cancer cells in the present study. All derivatives share a common pentacyclic triterpenoid core and the molecules were split into three pieces by cutting at the C-3 and C-28 sites with a consideration toward structural diversity. The analysis gave a leave-one-out cross-validation q2 value of 0.722 and a non-cross-validation r2 value of 0.974, which suggested that the model has good predictive ability (q2 > 0.2). The contour maps illustrated that bulky and electron-donating groups would be favorable for activity at the C-28 site, and a moderately bulky and electron-withdrawing group near the C-3 site would improve this activity. BE derivatives were designed and synthesized according to the modeling result, whereby bulky electronegative groups (maleyl, phthalyl, and hexahydrophthalyl groups) were directly introduced at the C-28 position of BE. The in vitro cytotoxicity values of the given analogs against HT29 cells were consistent with the predicted values, proving that the present topomer CoMFA model is successful and that it could potentially guide the synthesis of new betulinic acid derivatives with high anti-cancer activity. The IC50 values of these three new compounds were also assayed in five other tumor cell lines. 28-O-hexahydrophthalyl BE exhibited the greatest anti-cancer activities and its IC50 values were lower than those of BA in all cell lines, excluding DU145 cells. Full article
(This article belongs to the Section Medicinal Chemistry)

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