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Phenolic Substances and Biological Activities of Verbana officinalis L.: A Mini-Review 马鞭草酚类物质及其生物活性综述
Pub Date : 2020-02-05 DOI: 10.19080/omcij.2019.09.555758
Ghayth Rigane
The published data related to the identification of the major phenolic compounds as well as its biological activities present in Verbana officinalis L. This plant has received a great interest in the worldwide for its diuretic, expectorant and anti-rheumatic, anti-inflammatory, antifungal, antibacterial, analgesic and antioxidant activities.
马鞭草具有利尿、化痰、抗风湿、抗炎、抗真菌、抗菌、镇痛和抗氧化等作用,已发表的有关马鞭草中主要酚类化合物及其生物活性的鉴定资料在世界范围内引起了极大的兴趣。
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引用次数: 1
Noscapine as Anticancer Agent & Its Role in Ovarian Cancer 诺斯卡平的抗癌作用及其在卵巢癌中的作用
Pub Date : 2019-12-12 DOI: 10.19080/omcij.2019.09.555757
Ramesh Chandra
Cancer is a public health problem accounting for an estimated 9.6 million deaths worldwide, according to the latest WHO report, mainly affecting low-middle income countries. Noscapine (narcotize), a non-toxic benzylisoquinoline alkaloid derived from opium poppy, is commonly used as a cough suppressant in humans and exhibited various activities against a variety of cancers with unclear mechanism of action. Unlike other alkaloids obtained from opium poppy, noscapine is not sleep-inducing, hypnotic drug, rendering it as non-addictive drug and therefore used as antimitotic & antitussive drug around the world, can be orally consumed. Ovarian Cancer is one of the common causes of gynecologic cancer affecting women around the world. The main reason for treatment failure and mortality is the drug resistance against DDP (cisplatin), which has emerged the use of Noscapine against drug-resistant ovarian cancer cell line SKOV3/DDP by activation of apoptosis. Herein, we will describe noscapine chemically; its medicinal utility and pharmacological history behind the noscapine family of compounds then follow its journey for treating ovarian cancer (Figure 1).
根据世界卫生组织的最新报告,癌症是一个公共卫生问题,全世界约有960万人死于癌症,主要影响中低收入国家。诺斯卡平是一种从罂粟中提取的无毒苯异喹啉类生物碱,常被用作人类止咳药,对多种癌症具有多种活性,但作用机制尚不清楚。与从罂粟中提取的其他生物碱不同,诺斯卡平不是睡眠诱导、催眠药物,使其成为非成瘾性药物,因此在世界各地用作抗有丝分裂和止咳药,可以口服。卵巢癌是影响世界各地妇女的妇科癌症的常见原因之一。治疗失败和死亡的主要原因是对DDP(顺铂)的耐药,诺斯平通过激活细胞凋亡来治疗耐药卵巢癌细胞系SKOV3/DDP。在这里,我们将描述诺斯卡平的化学性质;诺斯卡平家族化合物背后的药用效用和药理学历史,然后跟随其治疗卵巢癌的历程(图1)。
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引用次数: 1
Synthesis of Acridone Base Phenolic Compounds for Antibacterial Activity 吖啶酮类酚类化合物抗菌活性的合成
Pub Date : 2019-11-14 DOI: 10.19080/omcij.2019.09.555756
Afreen Begum
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引用次数: 0
Preliminary Phytochemical Screening of Seeds of Phytolacca Latbenia (Moq.) walte. A Wild Medicinal Plant of Tropical and Sub-Tropical Region of Pakistan 植物种子的植物化学初步筛选。巴基斯坦热带和亚热带地区的一种野生药用植物
Pub Date : 2019-11-13 DOI: 10.19080/omcij.2019.09.555754
S. Ijaz
Phytolacca latbenia (Moq.) walte locally known as Luber belonging to family Phytollacaceae is used in traditional medicine system and pharmaceutical industries as well. Whole plant is medicinally important. The aim of this study was to analyze the seeds of Phytolacca latbenia (Moq.) Walte physico-chemically and phytochemically. Various bioactive compounds (alkaloids, terpenoids, favonoids, saponins, carbohydrate, proteins etc) were detected in water extract, while other solvents were not ideal for extraction few compounds were screened out from them. High extraction was done by water solvent and low value was in acetone solvent. Seeds of Phytolacca latbenia showed variety of therapeutic potential due to the presence of several phytochemical compounds.
植物科植物(Phytolacca latbenia, Moq.)在当地被称为Luber,在传统医药系统和制药工业中也有广泛的应用。整株植物具有重要的药用价值。本研究的目的是对植物的种子进行分析。沃尔特:物理化学和植物化学。水提物中检出多种生物活性物质(生物碱、萜类、黄酮类、皂苷、碳水化合物、蛋白质等),而其他溶剂不适合提取,从中筛选出少量化合物。水溶剂提取率高,丙酮溶剂提取率低。由于其含有多种植物化学成分,因此具有丰富的药用价值。
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引用次数: 2
A Review of 2,4-D Environmental Fate, Persistence and Toxicity Effects on Living Organisms 2,4- d对生物的环境命运、持久性和毒性作用研究进展
Pub Date : 2019-11-13 DOI: 10.19080/omcij.2019.09.555755
Chali Abate Jote
2,4-D is one of the most used herbicides in the world. It has been used since 1940s and its popularity seems to be increasing. Due to its broad range of application and excessive usage, it has becoming a serious problem as it can cause pollution to the environment. Extensive researches have been done for 2,4-D but comparatively few for its derivatives. Therefore, in this review article, I focused on 2,4-D environmental fates, persistence and effects on living organisms. Hence, its toxicity levels, toxicity classification and ecotoxicity studies were reviewed based on available references. In this review article, also discussed the toxicity effects of 2,4-D on animals and humans.
2,4- d是世界上使用最多的除草剂之一。自20世纪40年代以来,它一直在使用,它的受欢迎程度似乎越来越高。由于它的广泛应用和过度使用,它已经成为一个严重的问题,因为它会对环境造成污染。对2,4- d进行了广泛的研究,但对其衍生物的研究相对较少。因此,在这篇综述文章中,我着重于2,4- d的环境命运,持久性和对生物体的影响。在此基础上,对其毒性水平、毒性分类和生态毒性研究进行了综述。本文还讨论了2,4- d对动物和人体的毒性作用。
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引用次数: 6
Are the Authors of Scientific Articles Protected Against Plagiarism? 27 Years of Experience Shows that Rather Plagiarists are Protected in the Peer Review System 科学论文的作者是否受到抄袭的保护?27年的经验表明,剽窃者在同行评审制度中受到保护
Pub Date : 2019-10-23 DOI: 10.19080/omcij.2019.09.555753
Á. Furka
The Author of this article in 1990 submitted for publishing a manuscript describing the split-mix combinatorial synthesis and the invention was expropriated and published by the Editor in Chief of International Journal of Peptide and Protein Research and all the three reviewers are suspected to do so. The Author tried to seek justice but it was refused by the Editor in chief of Nature (where the expropriated invention was published), by the Office of Research Integrity at NIH and by the by the Munksgaard International Publishers, Copenhagen, publisher of the International Journal of Peptide and Protein Research. Since the plagiarists continued to publish misleading papers the Author sent 10 correction letters to the journals but only three were published. The Committee on Ethics of the American Chemical Society also refrained from acting. In order to avoid happening again of the mentioned type of plagiarism, introduction of new rules is suggested by the Author.
这篇文章的作者在1990年提交了一份描述分裂混合组合合成的手稿,该发明被国际肽和蛋白质研究杂志的主编没收并发表,怀疑所有三位审稿人都这样做了。作者试图寻求正义,但被《自然》杂志(被征用的发明发表在该杂志上)主编、美国国立卫生研究院研究诚信办公室和《国际肽和蛋白质研究杂志》的出版商哥本哈根Munksgaard国际出版商拒绝了。由于抄袭者继续发表误导性的论文,作者给这些期刊发了10封更正信,但只有3封被发表。美国化学会伦理委员会也没有采取行动。为了避免上述类型的抄袭再次发生,作者建议引入新的规则。
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引用次数: 0
Synthesis and Characterization of New Biologically Active Pyrrolo[2,3-b]Pyridine Scaffolds 新型生物活性吡咯[2,3-b]吡啶支架的合成与表征
Pub Date : 2019-09-16 DOI: 10.19080/omcij.2019.09.555752
Farid M Sroor
The 4-amino-1-(2,4-dichlorophenyl)-3-(3,4-dimethoxyphenyl)-6-phenyl-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile, 8 and 4-amino- 6-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-3-(3,4-dimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile, 9 were prepared and fully characterized by reaction of the new 2-amino-1-(2,4-dichlorophenyl)-4-(3,4-dimethoxyphenyl)-1H-pyrrole-3-carbonitrile 4 with 2-arylidenemalononitriles 6 and 7 in ethanol and the presence of piperidine (1 mL) to afford 8 and 9 in excellent yield 87% and 91%, respectively.
4-氨基-1-(2,4-二氯苯基)-3-(3,4-二甲氧基苯基)-6-苯基- 1h -吡咯[2,3-b] -5-碳腈,8和4-氨基-6-(4-氯苯基)-1-(2,4-二氯苯基)-3-(3,4-二甲氧基)- 1h -吡咯[2,3-b] -5-碳腈,采用2-氨基-1-(2,4-二氯苯基)-4-(3,4-二甲氧基苯基)- 1h -吡咯-3-碳腈4与2-芳基二甲基腈6和7在乙醇和哌替啶的存在(1 mL)下反应,制备了8和9,产率分别为87%和91%。
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引用次数: 0
Influence of Donor and Acceptor Substituents in 1,3-Oxazole Derivatives and Their Anti-Cancer Activity 1,3-恶唑衍生物中供体和受体取代基的影响及其抗癌活性
Pub Date : 2019-09-13 DOI: 10.19080/omcij.2019.09.555751
Nataliya V Obernikhina
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引用次数: 0
Synthesis and Cytotoxicity Evaluation of Some New 4-(4oxo-4H-Quinazoline-3yl)- Thiobenzoic Acid-S-(1-H-Benzimidazole-2-Yl) Ester Derivates 新型4-(4oxo- 4h -喹唑啉-3基)-硫代苯甲酸- s -(1- h -苯并咪唑-2基)酯衍生物的合成及细胞毒性评价
Pub Date : 2019-09-11 DOI: 10.19080/omcij.2019.08.555750
F. Hassanzadeh
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引用次数: 0
Electrochemical Determination of Ascorbic Acid in Pharmaceutical Tablets using Carbon Paste Electrode 碳糊电极电化学测定片剂中的抗坏血酸
Pub Date : 2019-08-30 DOI: 10.19080/omcij.2019.08.555749
Meareg Amare
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引用次数: 8
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