Proceedings of 5th International Electronic Conference on Medicinal Chemistry最新文献

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Antistaphylococcal activity of new salicylamide analogues 新型水杨胺类似物的抗葡萄球菌活性
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-31 DOI: 10.3390/ecmc2019-06344
Hana Michnová, A. Imramovský, Pratibha Magar, A. Čížek, J. Jampílek
{"title":"Antistaphylococcal activity of new salicylamide analogues","authors":"Hana Michnová, A. Imramovský, Pratibha Magar, A. Čížek, J. Jampílek","doi":"10.3390/ecmc2019-06344","DOIUrl":"https://doi.org/10.3390/ecmc2019-06344","url":null,"abstract":": Antimicrobial resistance is still a serious global threat. Staphylococcus aureus is a common cause of severe infections in health facilities and the community. People with methicillin-resistant S. aureus (MRSA) are estimated to be 64% more likely to die than people with a non-resistant form of the infection. For that reason, the research and development of new active compounds is really needed. Salicylamides are anti-infectious agents with a wide range of pharmacological effects, such us antiviral, antibacterial, antifungal and anthelminthic. Thus, derivatives of this group are very promising compounds. A series of newly synthesized complex salicylamide derivatives was tested for their antimicrobial effect against methicillin-resistant Staphylococcus aureus (MRSA). Staphylococcus aureus ATCC 29213 as a control and three isolates of MRSA were used. The activity was assessed by the evaluation of minimum inhibitory concentration. Using the microdilution method with subcultivation of aliquots, the minimum bactericidal concentration was determined too. Ciprofloxacin and ampicillin were used as standard antibacterial drugs. Four most promising compounds from the series were chosen and are demonstrated in this contribution.","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115727282","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Food for celiacs with black quinoa (Chenopodium petiolare kunth) 用黑藜麦(Chenopodium petiolare kunth)治疗乳糜泻的食物
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-31 DOI: 10.3390/ecmc2019-06347
Juan B Beltramino, M. Mesa, S. Soto
{"title":"Food for celiacs with black quinoa (Chenopodium petiolare kunth)","authors":"Juan B Beltramino, M. Mesa, S. Soto","doi":"10.3390/ecmc2019-06347","DOIUrl":"https://doi.org/10.3390/ecmc2019-06347","url":null,"abstract":"","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"45 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115788297","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chemical imaging in pharmaceutics for formulation analysis, quality control, and monitoring of formulation interactions with biological tissue 药剂学中用于制剂分析、质量控制和制剂与生物组织相互作用监测的化学成像
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-31 DOI: 10.3390/ecmc2019-06351
I. Iermak, Ana Paula Silva, C. Kurachi, V. Bagnato, N. Inada
{"title":"Chemical imaging in pharmaceutics for formulation analysis, quality control, and monitoring of formulation interactions with biological tissue","authors":"I. Iermak, Ana Paula Silva, C. Kurachi, V. Bagnato, N. Inada","doi":"10.3390/ecmc2019-06351","DOIUrl":"https://doi.org/10.3390/ecmc2019-06351","url":null,"abstract":"Raman microspectroscopy is an elegant and efficient tool for chemical analysis of the samples since it provides information about the structure, conformation, and changes of molecules both in pharmaceutical formulation and in the biological tissue. It is especially useful for samples containing water since water absorption is not dominating the Raman spectrum, as it happens in the case of infrared spectroscopy. Analysis of several formulations for onychomycosis treatment is shown as the example of Raman microspectroscopy application in pharmaceutics. Differences between the formulations are shown to be linked to their efficiency in the infection treatment. Comparison of Raman microspectroscopy as the tool to analyze pharmaceutical formulations, their efficiency and stability is made in relation to the other spectroscopical and microscopical methods and the advantages and disadvantages of several techniques are discussed. The application of the results obtained in this study is demonstrated on further improvement of the formulation in development.","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"38 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130638827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In silico studies of bacterial efflux pump inhibition by thioxanthones and their synergistic antibacterial activity 硫代蒽酮抑制细菌外排泵及其协同抗菌活性的硅片研究
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06300
E. Sousa, Fernando Durães, F. Barbosa, Joana Freitas-Silva, Paulo M. Costa, M. Pinto
{"title":"In silico studies of bacterial efflux pump inhibition by thioxanthones and their synergistic antibacterial activity","authors":"E. Sousa, Fernando Durães, F. Barbosa, Joana Freitas-Silva, Paulo M. Costa, M. Pinto","doi":"10.3390/ecmc2019-06300","DOIUrl":"https://doi.org/10.3390/ecmc2019-06300","url":null,"abstract":"","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"49 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123149080","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Novel synthesis of 3-fluoro- and 3,3-difluoro-substituted β-lactams: evaluation as potential antiproliferative and tubulin destabilizing agents 新合成的3-氟和3,3-二氟取代β-内酰胺:作为潜在的抗增殖和微管蛋白不稳定剂的评价
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06303
Azizah M Malebari, M. Meegan
{"title":"Novel synthesis of 3-fluoro- and 3,3-difluoro-substituted β-lactams: evaluation as potential antiproliferative and tubulin destabilizing agents","authors":"Azizah M Malebari, M. Meegan","doi":"10.3390/ecmc2019-06303","DOIUrl":"https://doi.org/10.3390/ecmc2019-06303","url":null,"abstract":"","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"62 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128252441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acetylcholinesterase and antioxidant evaluation of C18-functionalized ferruginol analogues 乙酰胆碱酯酶和c18功能化铁氨酸类似物的抗氧化评价
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06313
Miguel A. González-Cardenete, A. Yuste, E. García-Martínez, M. Nicolai, R. Zaragozá, P. Rijo
{"title":"Acetylcholinesterase and antioxidant evaluation of C18-functionalized ferruginol analogues","authors":"Miguel A. González-Cardenete, A. Yuste, E. García-Martínez, M. Nicolai, R. Zaragozá, P. Rijo","doi":"10.3390/ecmc2019-06313","DOIUrl":"https://doi.org/10.3390/ecmc2019-06313","url":null,"abstract":"One slide, Max 200 words The abietane-type diterpenoids are characterized by a tricyclic ring system and have shown a wide range of chemical diversity and biological activity. Medicinal chemists have studied derivatives of two readily available materials such as dehydroabietic acid and dehydroabietylamine. To date, there is only one commercial drug, Ecabet® [ecabet sodium], based on abietanes, which is used for the treatment of reflux esophagitis and peptic ulcer disease. The simplest phenolic abietane, ferruginol, exhibits anticancer effects in human ovarian cancer and inhibition of cancer cell migration. It also has shown interesting properties in different models of Alzheimer’s disease, researchers have reported neuroprotective effects of ferruginol against amyloid-b (Aβ) oligomers-induced neurodegenerative alterations and butyrylcholinesterase inhibition. In this communication, we present the results of an investigation of several C18ferruginol analogues on anti-acetylcholinesterase activity and antioxidant agents.","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129689560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharma-toxicological and phytochemical investigations on Tanacetum parthenium and Salix alba extracts: Focus on potential application as anti-migraine agents 巴塞草和白柳提取物的药物毒理学和植物化学研究:重点研究抗偏头痛药物的潜在应用
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06282
C. Ferrante
{"title":"Pharma-toxicological and phytochemical investigations on Tanacetum parthenium and Salix alba extracts: Focus on potential application as anti-migraine agents","authors":"C. Ferrante","doi":"10.3390/ecmc2019-06282","DOIUrl":"https://doi.org/10.3390/ecmc2019-06282","url":null,"abstract":"Migraine is one of the most common neurological disorder, which has long been related to brain serotonin (5-HT) depletion and neuro-inflammation. Despite many treatment options are available, the frequent occurrence of unacceptable adverse effects further supports the research toward nutraceuticals and herbal preparations, among which Tanacetum parthenium and Salix alba showed promising anti-inflammatory and neuro-modulatory activities. \u0000The impact of extract treatment on astrocyte viability, spontaneous migration and apoptosis was evaluated. Anti-inflammatory/anti-oxidant effects were investigated on isolated rat cortexes exposed to a neurotoxic stimulus. The lactate dehydrogenase (LDH) release, nitrite levels and 5-HT turnover were evaluated, as well. A proteomic analysis was focused on specific neuronal proteins and a fingerprint analysis was carried out on selected phenolic compounds. \u0000Both extracts appeared able to exert in vitro anti-oxidant and anti-apoptotic effects. S. alba and T. parthenium extracts reduced LDH release, nitrite levels and 5-HT turnover induced by neurotoxicity stimulus. The downregulation of selected proteins suggest a neurotoxic, which could be ascribed to an elevate content of gallic acid in both S. alba and T. parthenium extracts. \u0000Concluding, both extracts exert neuroprotective effects, although the downregulation of key proteins involved in neuron physiology suggest caution in their use as food supplements.","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"35 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116298076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interactions of zinc(II) complexes with N-donor ligands with 5’-GMP and their cytotoxic activity 锌(II)配合物与n -供体配体与5′-GMP的相互作用及其细胞毒活性
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06286
T. Soldatović, Enisa Selimović, Biljana M Šmit, Darko P Ašanin, Nevena S. Planojević, S. Marković, R. Puchta, B. M. Alzoubi
{"title":"Interactions of zinc(II) complexes with N-donor ligands with 5’-GMP and their cytotoxic activity","authors":"T. Soldatović, Enisa Selimović, Biljana M Šmit, Darko P Ašanin, Nevena S. Planojević, S. Marković, R. Puchta, B. M. Alzoubi","doi":"10.3390/ecmc2019-06286","DOIUrl":"https://doi.org/10.3390/ecmc2019-06286","url":null,"abstract":"Design of novel non-platinum DNA and protein targeting metal-based anticancer agents with potential in vitro toxicity have gained importance in recent years (Bertini, I. et al, Biological Inorganic Chemistry. Structure and Reactivity. University Science Books. Sausalito, CA. 2007. The non-platinum antitumor complexes could be alternatives to platinum-based drugs due to their better characteristics and less negative side effects. (Pessoa, J.C., et al. J. Inorg. Biochem. 2011, 105, 637-644). \u0000The mechanism of substitution from tetrahedral [ZnCl2(en)] and square-pyramidal [ZnCl2(terpy)] complexes (where en = 1,2-diaminoethane or ethylenediamine; terpy= 2,2′:6′,2′′-terpyridine) by guanosine-5’-monophospahate (5’-GMP) have been investigated by 1H NMR spectroscopy. Information about the structures of the final products in solution were obtained from the DFT calculations (B3LYP/6-31G(d)) and experimental 1H NMR data acquired during the course of the reaction. The cytotoxic activity of zinc(II) complexes was tasted on human breast cancer cell line MDA-MB-231, human colon cancer cell line HCT-116 and normal human lung fibroblast cell line MRC-5. Both complexes reduced cell viabilities, while [ZnCl2(terpy)] complex was significantly cytotoxic on MDA-MB-231 after 72 h, and HCT-116 after 24 h without dose dependence. The differences in reactivity toward 5’-GMP and cytotoxic activity of Zn(II) complexes may be attributed to the very stable square-pyramidal geometry of [ZnCl2(terpy)] complex in solution, while weak ligand effect of the en compared to the terpy affected slow interaction of tetrahedral [ZnCl2(en)] complex with the target bio-molecule (Soldatovic, E., et al. J. Coord. Chem. 2019, 72(4), 690-706). \u0000Acknowledgements: T. Soldatovic and E. Selimovic gratefully acknowledge financial support from State University of Novi Pazar, Novi Pazar, Republic of Serbia. R. Puchta would like to thank the Regionales Rechenzentrum Erlangen (RRZE) for a generous allotment of computer time, Prof. Tim Clark for hosting this work at the CCC. B.M. Alzoubi thanks Al-Balqa Applied University for its support. The authors are grateful for the support to the Ministry of Education, Science and Techhnological Development of the Republic of Serbia (Projects No. III41010, OI172016 and OI172036)","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"179 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126072008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Design, synthesis, X-ray structure and evaluation of functionalized hexacyclic carbazoles as new inhibitors of ABCG2 transporter 新型ABCG2转运体抑制剂功能化六环咔唑的设计、合成、x射线结构及评价
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06343
A. Bouraiou, G. Valdameri, I. Zanzarini, Esma Lamera, S. Bouacida, I. Zattoni, D. Kita, Z. Bouaziz, V. R. Moure, M. B. Borgne
{"title":"Design, synthesis, X-ray structure and evaluation of functionalized hexacyclic carbazoles as new inhibitors of ABCG2 transporter","authors":"A. Bouraiou, G. Valdameri, I. Zanzarini, Esma Lamera, S. Bouacida, I. Zattoni, D. Kita, Z. Bouaziz, V. R. Moure, M. B. Borgne","doi":"10.3390/ecmc2019-06343","DOIUrl":"https://doi.org/10.3390/ecmc2019-06343","url":null,"abstract":"","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"30 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121437941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Antioxidant capacity and cholinesterase inhibitory activity of Vulpicida pinastri lichen and its chemical composition 刺槐地衣的抗氧化能力、抑制胆碱酯酶活性及其化学成分
Proceedings of 5th International Electronic Conference on Medicinal Chemistry Pub Date : 2019-10-30 DOI: 10.3390/ecmc2019-06317
Isabel Maria Ureña Vacas, Elena González Burgos, M. Gómez-Serranillos
{"title":"Antioxidant capacity and cholinesterase inhibitory activity of Vulpicida pinastri lichen and its chemical composition","authors":"Isabel Maria Ureña Vacas, Elena González Burgos, M. Gómez-Serranillos","doi":"10.3390/ecmc2019-06317","DOIUrl":"https://doi.org/10.3390/ecmc2019-06317","url":null,"abstract":"","PeriodicalId":312909,"journal":{"name":"Proceedings of 5th International Electronic Conference on Medicinal Chemistry","volume":"9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117268597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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