Activity Prediction of Various Herbicides against Honey Bee, Avian, and Multiple Human Leukemia, CNS, Ovarian, Prostate Cancer Cell Lines

K. Hammud
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Abstract

Herbicides classify as chemicals targeting specific biochemical pathways in plants and may influence human or animal health according to their chemistry, concentration, environment, biological target and others. With safety concern, International Agency for Research on Cancer (IARC) classified herbicides and their metabolites as fetal developments may be a consequence of enzymatic inhibition or other mechanisms. Thirty phytotoxins were subjected to online pkCSM website, as a Quantitative Structure Activity Relationship (QSAR) prediction activity against honey bee, avian, and multiple human Leukemia, CNS, Ovarian, Prostate Cancer cell lines. Prediction outcomes were varied and influenced by chemical structure of each tested herbicide. Sulfentrazone having evidence of human non- carcinogenic character (Group E) had hepatotoxicity prediction and cancer cell lines activity less than 5 of Leukemia, CNS, Ovarian, and Prostate. Also, it had CYP1A2 inhibition, negative response of p- glycoprotein, Ames, skin sensitization, renal OCT2, and hERG. All above characters beside low intestinal absorption and Blood- Brain Barrier (BBB) presented encouraging online funding as more structurally safe having active – multiple toxicological and cellular interactions. Simetryn and Simazine that have the same core structure except (-SCH3) group replaced with chloro group gave semi identical results of many calculated characters and inactive materials to cancer cell lines and herbicide activity, honey bee and avian toxicities but not BBB, total clearance, and oral rat chronic (LOAEL) confirming structure influences upon prediction.
各种除草剂对蜜蜂、鸟类和多种人类白血病、中枢神经系统、卵巢癌、前列腺癌细胞的活性预测
除草剂是一种针对植物特定生化途径的化学品,根据其化学性质、浓度、环境、生物靶标等因素,可能影响人类或动物的健康。出于安全考虑,国际癌症研究机构(IARC)将除草剂及其代谢物归类为胎儿发育可能是酶抑制或其他机制的结果。利用pkCSM网站对30种植物毒素进行了定量结构活性关系(QSAR)预测,对蜜蜂、鸟类和多种人类白血病、中枢神经系统、卵巢癌、前列腺癌细胞系进行了活性预测。每种除草剂的化学结构对预测结果有不同的影响。磺胺曲酮具有人类非致癌性(E组)的肝毒性预测和白血病、中枢神经系统、卵巢癌和前列腺癌细胞系活性低于5。CYP1A2抑制,p-糖蛋白、Ames、皮肤致敏、肾OCT2、hERG均呈阴性反应。除了低肠吸收和血脑屏障(BBB)之外,所有这些特性都是鼓励在线资助的,因为它们结构更安全,具有积极的多重毒理学和细胞相互作用。Simetryn和Simazine的核心结构相同,除了(-SCH3)基团被氯基团取代外,它们对癌细胞的许多计算特性和无活性物质以及除草剂活性、蜜蜂和鸟类毒性的结果都是半相同的,但BBB、总清除率和口服大鼠慢性(LOAEL)的结果不一致,证实了结构对预测的影响。
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