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Screening of Anticancer Potential and DNA Damage Ability ofSyringodium isoetifolium against HeLa Cell Line 异叶丁香抗HeLa细胞潜能及DNA损伤能力的筛选
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p381
M. Pradeep, V. Shudarsan, M. Kaviraj, V. Lakshimi, D. Satheesh
Cervical cancer is a kind of cancer, which mainly occurs in the lower portion of uterus. Human papilloma virus plays a major role in the occurrence of cervical cancer. Major symptoms are vaginal bleeding, foul odour in vagina, pelvic pain, etc. It is mostly diagnosed by biopsy. Chemotherapy, radiation and surgery are the widely used treatments for cervical cancer, but the main drawback was their side effects. To avoid these conditions people might follow the ancient methods of treatment. Medicinal plants got wide attention in the current society to cure various diseases. The seagrass obtained from the seashores possess a wide range of medicinal properties like anticancer activity. In this study, the anticancer potentials of the seagrass, Syringodium isoetifolium was checked with the help of MTT and Comet assays. The various functional compounds present in the seagrass were also detected by FT-IR analysis. From the results obtained from MTT assay, the least inhibitory concentration of the sample was found to be 35.63 μg/mL. Further results obtained from the Comet assay prove that the sample has the ability to kill the cancer cells. This study concludes that the methanolic extract of Syringodium isoetifolium can be used as an alternative and marine based source for the treatment of cervical cancer.
宫颈癌是一种主要发生在子宫下部的癌症。人乳头瘤病毒在子宫颈癌的发生中起主要作用。主要症状为阴道出血、阴道异味、盆腔疼痛等。它大多是通过活检诊断的。化疗、放疗和手术是宫颈癌广泛使用的治疗方法,但主要缺点是它们的副作用。为了避免这些情况,人们可能会遵循古老的治疗方法。药用植物治疗各种疾病在当今社会受到广泛关注。从海岸获得的海草具有广泛的药用特性,如抗癌活性。本研究采用MTT法和comet法研究了海草紫丁香的抗癌作用。利用傅里叶变换红外光谱分析,对海草中存在的各种功能化合物进行了检测。MTT法测定样品的最低抑菌浓度为35.63 μg/mL。彗星试验的进一步结果证明,该样品具有杀死癌细胞的能力。综上所述,丁香醇提物可作为一种替代的海洋来源用于宫颈癌的治疗。
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引用次数: 0
Exploring 3D QSAR Study of Pyridone-Pyrimidone Derivatives as GlucokinaseActivators in Treatment of Diabetes Mellitus by using CoMFA Method CoMFA法探讨吡啶酮-嘧啶酮衍生物作为葡萄糖激酶激活剂治疗糖尿病的三维QSAR研究
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p360
Priyanka N. Chhajed, R. B. Patil
In this work, we have performed 3D QSAR study of reported pyridone-pyrimidone derivatives. CoMFA was applied to generate 3D QSAR models. Total eight QSAR models were generated. Model 2 was close to standard set criteria. Effect of steric and electrostatic substituents on biological activity was observed on contour maps. This study will be helpful for future researchers in designing new pyridinepyrimidone derivatives.
在这项工作中,我们对已报道的吡啶酮-嘧啶酮衍生物进行了3D QSAR研究。应用comfa3生成QSAR三维模型。共生成8个QSAR模型。模型2接近标准设定标准。在等高线图上观察了立体和静电取代基对生物活性的影响。本研究为今后研究人员设计新的吡啶嘧啶类衍生物提供了参考。
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引用次数: 0
Ultrasound Assisted New Imines of 3E-3-(4-Substituted benzylidene)-4-(substituted-1,3,4-thiadiazole-2-ylimino)pentane-2-one and their Antimicrobial Studies 超声辅助3E-3-(4-取代苄基)-4-(取代-1,3,4-噻二唑-2-酰基)戊烷-2- 1的新亚胺及其抗菌研究
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p364
M.B. Zade, S. N. Ibatte
A new series of Schiff bases of 3-(4-substituted benzylidene)-4-(substituted-1,3,4-thiadiazole-2- ylimino)pentane-2-one having various substituents of aryl attached to acetoacetone by Knovengel condensation and substituted 1,3,4-thiadiazole were synthesized by using solid supported tetrabutylammonium hydrogen sulfate in microwave irradiation. The synthesized Schiff bases have been evaluated by 1H NMR, elemental analysis, FTIR, mass spectroscopy. All Schiff bases have been screened for their antimicrobial activities. These compounds possess good result of antimicrobial studies.
采用固体负载硫酸氢四丁基铵在微波辐照下合成了一系列新的希夫碱:3-(4-取代苄基)-4-(取代-1,3,4-噻二唑-2-酰基)戊烷-2- 1,具有不同的芳基取代基,通过knovengel缩合与乙酰丙酮和取代1,3,4-噻二唑相连。对合成的席夫碱进行了1H NMR、元素分析、FTIR、质谱等表征。所有的希夫碱都经过了抗菌活性筛选。这些化合物具有良好的抗菌效果。
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引用次数: 0
Review Paper on Net Zero Energy Buildings 净零能耗建筑检讨文件
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.7-1-sp4.pp48-50
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引用次数: 2
Stabilization Using Fly Ash of Clayey Soil – A Review 粉煤灰在粘性土中的稳定研究进展
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.7-1-sp4.pp83-85
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引用次数: 0
Pharmacological Investigation of Fluoro, Iodo and Hydroxy Derivative ofChloro Substituted Homoisoflavonoids 氯代同型异黄酮的氟、碘和羟基衍生物的药理研究
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p357
D. Gaikwad, R. Murkute, S. Gaikwad
In present study, the synthesized substituted homoisoflavonoid derivatives were screened for their in vivo/in vitro antiarthritic activity, in vitro anti-inflammatory and DPPH free radical scavenging activity. The male Wistar rats were used for investigation of in vivo antiarthritic activity against complete freund’s adjuvant (CFA) induced arthritis and assessment was done for change in paw volume, serum marker enzymes (ALP, SGOT and SGPT) and membrane stabilization potential. in vitro anti-inflammatory activity was assessed by the protein denaturation method. In vitro free radical scavenging activity was assessed by the DPPH method. The result indicated that compound HIFa showed a significant antiarthritic activity as compared to other substituted homoisoflavonoid derivatives. The significant membrane stabilization and inhibition of protein denaturation showed in vitro antiarthritic and antiinflammatory activity of substituted homoisoflavonoid derivatives. The substituted homoisoflavonoid derivatives showed dose dependent DPPH free radical scavenging activity. From the present study, it was observed that the iodo derivative of substituted homoisoflavonoid derivatives have significant pharmacological activities as compared to floro and hydroxyl derivatives.
本研究对合成的取代类同型异黄酮衍生物进行体内/体外抗关节炎、体外抗炎和DPPH自由基清除活性的筛选。采用雄性Wistar大鼠,研究其体内抗CFA性关节炎的活性,评估其足部体积、血清标记酶(ALP、SGOT和SGPT)和膜稳定电位的变化。体外抗炎活性用蛋白变性法测定。采用DPPH法测定其体外自由基清除能力。结果表明,与其他取代的同型异黄酮衍生物相比,化合物HIFa具有明显的抗关节炎活性。取代的异黄酮衍生物具有明显的膜稳定作用和抑制蛋白变性的作用,具有体外抗关节炎和抗炎活性。取代的同型异黄酮衍生物具有剂量依赖性的DPPH自由基清除活性。从本研究中,我们观察到碘衍生物取代的同型异黄酮衍生物具有显著的药理活性相比,氟和羟基衍生物。
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引用次数: 0
A Review on the Strength Aspects of Light Weight Concrete Using Ultra-light Weight Foamed Glass Aggregate 超轻泡沫玻璃骨料轻混凝土强度研究进展
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.7-1-sp4.pp17-19
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引用次数: 0
Microwave Assisted a Highly Atom Economic, Chemo-, Regio- andStereoselective Synthesis and Evaluation of Dispiro[1H-indene-2,3′-pyrrolidine-2′,3′′-[3H]indole]-1,2′′(1′′H)diones as Antibacterial and Antifungal Agents 微波辅助下高原子经济性、化学选择性、区域选择性和立体选择性合成[1h -茚-2,3 ' -吡咯烷-2 ',3 " -[3H]吲哚]-1,2 " (1 " H)二酮类抗菌和抗真菌药物的评价
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p356
M. Kaleeswari, P. S. Harikrishnan
1,3-Dipolar cycloaddition of in situ generated non-stabilized azomethine ylides through the decarboxylative condensation of sarcosine and substituted isatins with 2-(arylmethylene)-2,3-dihydro-1H-inden-1-ones in microwave produced dispiro[1H-indene-2,3Œ-pyrrolidine-2Œ,3ŒŒ-[3H]indole]-1,2ŒŒ(1ŒŒH)diones in a highly stereo- and regio-selective fashion. The synthesized compounds were subjected to antibacterial and antifungal studies. It was found that many compounds possess a considerable antibacterial and antifungal activity against all the tested organisms.
以高度立体和区域选择性的方式,用2-(芳基亚甲基)-2,3-二氢- 1h -吲哚-1- Œ- Œ-[3H]吲哚]-1,2 - Œ- Œ(1′Œ′ŒH)二酮,对肌氨酸和取代的isatins进行脱羧缩合,原位生成非稳定的偶极环加成,得到了dispiro[1h -吲哚-2,3′Œ-pyrrolidine-2′Œ,3′Œ′Œ] 1,2′Œ′Œ(1′Œ′ŒH)二酮。合成的化合物进行了抗菌和抗真菌研究。发现许多化合物对所有被试生物都具有相当的抗菌和抗真菌活性。
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引用次数: 0
Synthesis, Characterization, Antimalarial and Anticancer Activities ofFew New Amino Analogues of 1,4-Naphthoquinone 1,4-萘醌氨基类似物的合成、表征及抗疟抗癌活性研究
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.ajomc-p372
S. Sanjay, Shashiprabha, K. Shridhara, K. Nagarajan, H. Sivaramakrishnan, B. Arun
Present study involves the synthesis, characterization, antimalarial and anticancer activities of some novel substituted amino analogues of 1,4-naphthoquinone. The chloro group present in the key starting materials like 2,3-dichloro-1,4-naphthoquinone (1) and 2-chloro-3-[trans-4-(4-chlorophenyl)- cyclohexyl]-1,4-naphthoquinone (2) was replaced by substituted amines. These analogues were isolated, purified and screened for antimalarial and anticancer activities. A few of the novel compounds were found to possess substantial biological activity and are reasonably potent.
本文主要研究了1,4-萘醌氨基类似物的合成、表征及其抗疟和抗癌活性。关键原料2,3-二氯-1,4-萘醌(1)和2-氯-3-[反式-4-(4-氯苯基)-环己基]-1,4-萘醌(2)中的氯基团被取代胺取代。对这些类似物进行了分离纯化,并进行了抗疟和抗癌活性筛选。一些新化合物被发现具有实质性的生物活性,并且相当有效。
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引用次数: 0
To Study the Effect of Unbalancing on Two Overhung Rotors by Vibration Monitoring 通过振动监测研究不平衡对双悬挑转子的影响
Pub Date : 2022-01-01 DOI: 10.14233/ajomc.2022.7-1-sp4.pp235-238
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引用次数: 0
期刊
Asian Journal of Organic & Medicinal Chemistry
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