Zeitschriftenartikel zum Thema „Anti-MRSA activity“
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Asnani, Ari, Eva Luviriani und Oedjijono Oedjijono. „Activity of Actinomycetes Isolated from Mangrove Segara Anakan Cilacap toward Methicillin-resistant Staphylococcus aureus (MRSA)“. Jurnal Kimia Sains dan Aplikasi 23, Nr. 1 (06.12.2019): 1–7. http://dx.doi.org/10.14710/jksa.23.1.1-7.
Kubo, Isao, Ping Xiao und Ken'ichi Fujita. „Anti-MRSA activity of alkyl gallates“. Bioorganic & Medicinal Chemistry Letters 12, Nr. 2 (Januar 2002): 113–16. http://dx.doi.org/10.1016/s0960-894x(01)00663-1.
Yao, Cheng-Jiao, Yi-lin Li, Meng-Jun Pu, Li-Hong Luo, Qin Xiong, Feng-Jiao Xie, Ting-Lin Li und Pei-Min Feng. „Aminoglycosides with Anti-MRSA Activity: A Concise Review“. Current Topics in Medicinal Chemistry 21, Nr. 27 (08.12.2021): 2483–99. http://dx.doi.org/10.2174/1568026621666211004093647.
Yao, Cheng-Jiao, Yi-lin Li, Meng-Jun Pu, Li-Hong Luo, Qin Xiong, Feng-Jiao Xie, Ting-Lin Li und Pei-Min Feng. „Aminoglycosides with Anti-MRSA Activity: A Concise Review“. Current Topics in Medicinal Chemistry 21, Nr. 27 (08.12.2021): 2483–99. http://dx.doi.org/10.2174/1568026621666211004093647.
Imamura, Hideaki, Norikazu Ohtake, Hideki Jona, Aya Shimizu, Minoru Moriya, Hiroki Sato, Yuichi Sugimoto et al. „Dicationic dithiocarbamate carbapenems with anti-MRSA activity“. Bioorganic & Medicinal Chemistry 9, Nr. 6 (Juni 2001): 1571–78. http://dx.doi.org/10.1016/s0968-0896(01)00044-x.
Ohtake, Norikazu, Hideaki Imamura, Hideki Jona, Hideo Kiyonaga, Aya Shimizu, Minoru Moriya, Hiroki Sato, Masato Nakano, Ryosuke Ushijima und Susumu Nakagawa. „Novel dithiocarbamate carbapenems with anti-MRSA activity“. Bioorganic & Medicinal Chemistry 6, Nr. 7 (Juli 1998): 1089–101. http://dx.doi.org/10.1016/s0968-0896(98)00069-8.
Ohtake, Norikazu, Hideaki Imamura, Hideo Kiyonaga, Hideki Jona, Masayuki Ogawa, Shigemitsu Okada, Aya Shimizu et al. „Novel dithiocarbamate carbapenems1 with anti-MRSA activity“. Bioorganic & Medicinal Chemistry Letters 7, Nr. 13 (Juli 1997): 1617–22. http://dx.doi.org/10.1016/s0960-894x(97)00272-2.
Yee, Cheung, Donald Biek, Kevin Krause und Gregory Williams. „Ceftaroline: a Cephalosporin with Anti-MRSA Activity“. Clinical Microbiology Newsletter 33, Nr. 21 (November 2011): 161–69. http://dx.doi.org/10.1016/j.clinmicnews.2011.10.001.
Cao, Feng, Wei Peng, Xiaoli Li, Ming Liu, Bin Li, Rongxin Qin, Weiwei Jiang et al. „Emodin is identified as the active component of ether extracts from Rhizoma Polygoni Cuspidati, for anti-MRSA activity“. Canadian Journal of Physiology and Pharmacology 93, Nr. 6 (Juni 2015): 485–93. http://dx.doi.org/10.1139/cjpp-2014-0465.
Yu, Moxi, Yachen Hou, Meiling Cheng, Yongshen Liu, Caise Ling, Dongshen Zhai, Hui Zhao et al. „Antibacterial Activity of Squaric Amide Derivative SA2 against Methicillin-Resistant Staphylococcus aureus“. Antibiotics 11, Nr. 11 (28.10.2022): 1497. http://dx.doi.org/10.3390/antibiotics11111497.
Gao, Yujie, Yuanhao Dong, Yubin Cao, Wenlong Huang, Chenhao Yu, Shangyan Sui, Anchun Mo und Qiang Peng. „Graphene Oxide Nanosheets with Efficient Antibacterial Activity Against Methicillin-Resistant Staphylococcus aureus (MRSA)“. Journal of Biomedical Nanotechnology 17, Nr. 8 (01.08.2021): 1627–34. http://dx.doi.org/10.1166/jbn.2021.3123.
Sundar, Ranjitha Dhevi V., und Sathiavelu Arunachalam. „Anti-MRSA activity of Pollianthes tuberosa leaf extracts“. Bangladesh Journal of Pharmacology 17, Nr. 1 (18.03.2022): 11–13. http://dx.doi.org/10.3329/bjp.v17i1.57727.
Zhao, Min, Tomonori Kamada, Aya Takeuchi, Hiromi Nishioka, Teruo Kuroda und Yasuo Takeuchi. „Structure–activity relationship of indoloquinoline analogs anti-MRSA“. Bioorganic & Medicinal Chemistry Letters 25, Nr. 23 (Dezember 2015): 5551–54. http://dx.doi.org/10.1016/j.bmcl.2015.10.058.
Rukavina, Zora, May Wenche Jøraholmen, Dunja Božić, Ivana Frankol, Petra Golja Gašparović, Nataša Škalko-Basnet, Maja Šegvić Klarić und Željka Vanić. „Azithromycin-loaded liposomal hydrogel: a step forward for enhanced treatment of MRSA-related skin infections“. Acta Pharmaceutica 73, Nr. 4 (01.12.2023): 559–79. http://dx.doi.org/10.2478/acph-2023-0042.
Kristiana, Rhesi, Gilles Bedoux, Gerard Pals, I. Wayan Mudianta, Laure Taupin, Christel Marty, Meezan Ardhanu Asagabaldan et al. „Bioactivity of compounds secreted by symbiont bacteria of Nudibranchs from Indonesia“. PeerJ 8 (02.01.2020): e8093. http://dx.doi.org/10.7717/peerj.8093.
Al Bshabshe, Ali, Martin R. P. Joseph, Amgad A. Awad El-Gied, Abdalla N. Fadul, Harish C. Chandramoorthy und Mohamed E. Hamid. „Clinical Relevance and Antimicrobial Profiling of Methicillin-Resistant Staphylococcus aureus (MRSA) on Routine Antibiotics and Ethanol Extract of Mango Kernel (Mangifera indica L.)“. BioMed Research International 2020 (19.02.2020): 1–8. http://dx.doi.org/10.1155/2020/4150678.
Xu, Li, Xuejie Xu, Ganjun Yuan, Yimin Wang, Yunqiu Qu und Erxiao Liu. „Mechanism of Azalomycin F5a against Methicillin-Resistant Staphylococcus aureus“. BioMed Research International 2018 (2018): 1–5. http://dx.doi.org/10.1155/2018/6942452.
Dai, Jie, Narsaiah Battini, Zhonglin Zang, Yan Luo und Chenghe Zhou. „Novel Thiazolylketenyl Quinazolinones as Potential Anti-MRSA Agents and Allosteric Modulator for PBP2a“. Molecules 28, Nr. 10 (22.05.2023): 4240. http://dx.doi.org/10.3390/molecules28104240.
Dong, Li-Mei, Li-Lan Huang, Hang Dai, Qiao-Lin Xu, Jin-Kui Ouyang, Xu-Chao Jia, Wen-Xiang Gu und Jian-Wen Tan. „Anti-MRSA Sesquiterpenes from the Semi-Mangrove Plant Myoporum bontioides A. Gray“. Marine Drugs 16, Nr. 11 (08.11.2018): 438. http://dx.doi.org/10.3390/md16110438.
Arnould, Jean Claude, Ruth N. Illingworth, Wright W. Nichols und R. Geoffrey Wilson. „Synthesis and antibacterial activity of lipophilic carbapenems with anti-MRSA activity“. Bioorganic & Medicinal Chemistry Letters 6, Nr. 20 (Oktober 1996): 2449–54. http://dx.doi.org/10.1016/0960-894x(96)00450-7.
Lee, Young-Seob, Dae-Young Lee, Yeon Bok Kim, Sang-Won Lee, Seon-Woo Cha, Hong-Woo Park, Geum-Soog Kim, Dong-Yeul Kwon, Min-Ho Lee und Sin-Hee Han. „The Mechanism Underlying the Antibacterial Activity of Shikonin against Methicillin-ResistantStaphylococcus aureus“. Evidence-Based Complementary and Alternative Medicine 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/520578.
Zhao, Hui, Lu Liu, Lingshuang Yang, Qihui Gu, Ying Li, Jumei Zhang, Shi Wu, Moutong Chen, Xinqiang Xie und Qingping Wu. „Pseudomonas protegens FJKB0103 Isolated from Rhizosphere Exhibits Anti-Methicillin-Resistant Staphylococcus aureus Activity“. Microorganisms 10, Nr. 2 (28.01.2022): 315. http://dx.doi.org/10.3390/microorganisms10020315.
Bueso-Bordils, Jose I., Pedro A. Alemán-López, Rafael Martín-Algarra, Maria J. Duart, Antonio Falcó und Gerardo M. Antón-Fos. „Molecular Topology for the Search of New Anti-MRSA Compounds“. International Journal of Molecular Sciences 22, Nr. 11 (29.05.2021): 5823. http://dx.doi.org/10.3390/ijms22115823.
Alshamsan, Aws, Fadilah Sfouq Aleanizy, Mohamed Badran, Fulwah Yahya Alqahtani, Haya Alfassam, Abdulaziz Almalik und Sara Alosaimy. „Exploring anti-MRSA activity of chitosan-coated liposomal dicloxacillin“. Journal of Microbiological Methods 156 (Januar 2019): 23–28. http://dx.doi.org/10.1016/j.mimet.2018.11.015.
D'Andrea, Stan V., Daniel Bonner, Joanne J. Bronson, Junius Clark, Ken Denbleyker, Joan Fung-Tomc, Shelley E. Hoeft et al. „Synthesis and anti-MRSA Activity of Novel Cephalosporin Derivatives“. Tetrahedron 56, Nr. 31 (Juli 2000): 5687–98. http://dx.doi.org/10.1016/s0040-4020(00)00418-x.
MUN, SU-HYUN, OK-HWA KANG, DAE-KI JOUNG, SUNG-BAE KIM, JANG-GI CHOI, DONG-WON SHIN und DONG-YEUL KWON. „In vitro anti-MRSA activity of carvone with gentamicin“. Experimental and Therapeutic Medicine 7, Nr. 4 (23.01.2014): 891–96. http://dx.doi.org/10.3892/etm.2014.1498.
Shin, Dongyun, Seong-Hyuk Park, Sooyoung Park, Chang-Yong Lee und Young-Ger Suh. „Efficient Synthesis of 1-Thiomansonones with Anti-MRSA Activity“. Synlett 29, Nr. 07 (29.01.2018): 938–42. http://dx.doi.org/10.1055/s-0036-1591894.
OHTAKE, N., H. IMAMURA, H. KIYONAGA, H. JONA, M. OGAWA, S. OKADA, A. SHIMIZU et al. „ChemInform Abstract: Novel Dithiocarbamate Carbapenems with anti-MRSA Activity.“ ChemInform 28, Nr. 46 (03.08.2010): no. http://dx.doi.org/10.1002/chin.199746236.
Aunpad, R., und K. Na-Bangchang. „P2085 A novel antimicrobial peptide with anti-MRSA activity“. International Journal of Antimicrobial Agents 29 (März 2007): S602. http://dx.doi.org/10.1016/s0924-8579(07)71924-6.
Iobbi, Valeria, Valentina Parisi, Giulia Bernabè, Nunziatina De Tommasi, Angela Bisio und Paola Brun. „Anti-Biofilm Activity of Carnosic Acid from Salvia rosmarinus against Methicillin-Resistant Staphylococcus aureus“. Plants 12, Nr. 21 (25.10.2023): 3679. http://dx.doi.org/10.3390/plants12213679.
Jieputra, Alden, Marijam Purwanta, Arifa Mustika und Wiwin Retnowati. „In vitro Antimicrobial Activity Test of Zingiber officinale var. rubrum Rhizome Extract against Methicillin-Sensitive Staphylococcus aureus (MSSA) and Methicillin-Resistant Staphylococcus aureus (MRSA)“. JUXTA: Jurnal Ilmiah Mahasiswa Kedokteran Universitas Airlangga 15, Nr. 1 (10.01.2024): 57–63. http://dx.doi.org/10.20473/juxta.v15i12024.57-63.
Prasad, H. S. Nagendra, A. P. Ananda, Amogh Mukarambi, Navyatha Prashanth Gaonkar, S. Sumathi, H. P. Spoorthy und P. Mallu. „Design, synthesis, and anti-bacterial activities of piperazine based phthalimide derivatives against superbug-Methicillin-Resistant Staphylococcus aureus“. Current Chemistry Letters 12, Nr. 1 (2023): 65–78. http://dx.doi.org/10.5267/j.ccl.2022.9.005.
Chabán, Macarena Funes, Antonia I Antoniou, Catherine Karagianni, Dimitra Toumpa, Mariana Belén Joray, José Luis Bocco, Claudia Sola, Constantinos M Athanassopoulos und María Cecilia Carpinella. „Synthesis and structure–activity relationships of novel abietane diterpenoids with activity against Staphylococcus aureus“. Future Medicinal Chemistry 11, Nr. 24 (Dezember 2019): 3109–24. http://dx.doi.org/10.4155/fmc-2019-0192.
Saravanakumar, Kandasamy, Ramachandran Chelliah, Xiaowen Hu, Deog-Hwan Oh, Kandasamy Kathiresan und Myeong-Hyeon Wang. „Antioxidant, Anti-Lung Cancer, and Anti-Bacterial Activities of Toxicodendron vernicifluum“. Biomolecules 9, Nr. 4 (29.03.2019): 127. http://dx.doi.org/10.3390/biom9040127.
Iizawa, Yuji, Junko Nagai, Tomoyasu Ishikawa, Shohei Hashiguchi, Masafumi Nakao, Akio Miyake und Kenji Okonogi. „In vitro antimicrobial activity of T-91825, a novel anti-MRSA cephalosporin, and in vivo anti-MRSA activity of its prodrug, TAK-599“. Journal of Infection and Chemotherapy 10, Nr. 3 (2004): 146–56. http://dx.doi.org/10.1007/s10156-004-0309-3.
Tsuchiya, Hironori, Masaru Sato, Nobuhiko Takaai und Munekazu Iinuma. „Phytotherapy for mixed MRSA infections: anti-MRSA and anti-candidal activity of chalcones and the combiotic effect with antibiotics.“ Japanese Journal of Pharmacology 71 (1996): 296. http://dx.doi.org/10.1016/s0021-5198(19)37424-4.
Berti, Andrew D., George Sakoulas, Victor Nizet, Ryan Tewhey und Warren E. Rose. „β-Lactam Antibiotics Targeting PBP1 Selectively Enhance Daptomycin Activity against Methicillin-Resistant Staphylococcus aureus“. Antimicrobial Agents and Chemotherapy 57, Nr. 10 (29.07.2013): 5005–12. http://dx.doi.org/10.1128/aac.00594-13.
Fadhlina, Anis, und Hassan Ibrahim Sheikh. „Anti-MRSA activity of Stereospermum fimbriatum’s stem bark extracted using subcritical and supercritical carbon dioxide“. IIUM Journal of Orofacial and Health Sciences 4, Nr. 2 (31.07.2023): 145–51. http://dx.doi.org/10.31436/ijohs.v4i2.221.
Tang, Kai-Wei, Shih-Chun Yang und Chih-Hua Tseng. „Design, Synthesis, and Anti-Bacterial Evaluation of Triazolyl-Pterostilbene Derivatives“. International Journal of Molecular Sciences 20, Nr. 18 (14.09.2019): 4564. http://dx.doi.org/10.3390/ijms20184564.
Jalil, Mohd Taufiq Mat, Nurul Aili Zakaria und Darah Ibrahim. „Effect of Culture Medium Incorporated with Ocimum sanctum Extract in Enhancing Anti-MRSA activity of Endophytic Fungus, Lasiodiplodia pseudotheobromae“. Journal of Pure and Applied Microbiology 15, Nr. 3 (31.07.2021): 1398–408. http://dx.doi.org/10.22207/jpam.15.3.32.
Johari, Saiful Azmi, Mastura Mohtar, Sharifah Aminah Syed Mohammad, Rohana Sahdan, Zurina Shaameri, Ahmad Sazali Hamzah und Mohd Fazli Mohammat. „In VitroInhibitory and Cytotoxic Activity of MFM 501, a Novel Codonopsinine Derivative, against Methicillin-ResistantStaphylococcus aureusClinical Isolates“. BioMed Research International 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/823829.
Ramya K A, Anu S. Sanker, Harish Kumar K. S, Shinu Krishnan und Neethu Babu. „Antibacterial Activity of Silver, Gold and AmoxicillinSilver Nanoparticles against Methicillin Resistant Staphylococcus aureus - an invitro Study“. International Journal of Current Research and Review 15, Nr. 10 (2023): 01–04. http://dx.doi.org/10.31782/ijcrr.2023.151001.
Subramaniam, Geetha, Rayshen Renganaden Poolee Cootee, Cheah Cheng Han und Lalita Ambigai Sivasamugham. „ANTI-BACTERIAL ACTIVITY OF Trigonella foenum-graecum AGAINST SKIN PATHOGENS“. Journal of Experimental Biology and Agricultural Sciences 9, Spl-1- GCSGD_2020 (25.03.2021): S110—S115. http://dx.doi.org/10.18006/2021.9(spl-1-gcsgd_2020).s110.s115.
Wei, Guoxing, und Yun He. „Antibacterial and Antibiofilm Activities of Novel Cyclic Peptides against Methicillin-Resistant Staphylococcus aureus“. International Journal of Molecular Sciences 23, Nr. 14 (21.07.2022): 8029. http://dx.doi.org/10.3390/ijms23148029.
Aguilera-Correa, John Jairo, Sara Fernández-López, Iskra Dennisse Cuñas-Figueroa, Sandra Pérez-Rial, Hanna-Leena Alakomi, Liisa Nohynek, Kirsi-Marja Oksman-Caldentey et al. „Sanguiin H-6 Fractionated from Cloudberry (Rubus chamaemorus) Seeds Can Prevent the Methicillin-Resistant Staphylococcus aureus Biofilm Development during Wound Infection“. Antibiotics 10, Nr. 12 (03.12.2021): 1481. http://dx.doi.org/10.3390/antibiotics10121481.
Walter, Sunette. „Antibacterial and anti-biofilm properties of Aptosimum albomarginatum(Marloth& Engl.) and Dicoma schinzii(O. Hoffm.) crude methanolic extracts against S. aureus and MRSA.“ Namibian Journal for Research, Science and Technology 3, Nr. 1 (31.05.2021): 69–77. http://dx.doi.org/10.54421/njrst.v3i1.44.
Sunazuka, T., A. Sugawara, K. Nagai, T. Hirose, Y. Yamaguchi, H. Hanaki, K. B. Sharpless und S. Omura. „‘Click Chemistry’ Synthesis of Macrolide Derivatives with Anti-MRSA and Anti-VRE Activity“. International Journal of Infectious Diseases 12 (Dezember 2008): e256-e257. http://dx.doi.org/10.1016/j.ijid.2008.05.694.
Mi, Qi-Li, Wei-Shong Kong, Yin-Ke Li, Xin Liu, Wan-Li Zeng, Hai-Ying Xiang, Dong Miao et al. „Chromone Derivatives Of Cassia pumila and their Anti-MRSA Activity“. Chemistry of Natural Compounds 57, Nr. 3 (Mai 2021): 432–35. http://dx.doi.org/10.1007/s10600-021-03381-3.
Kriushnapriya, S., N. S. Malathy, A. Shamitha Begum, A. C. Baskaran, B. Appalaraju, K. Mani und K. A. Kandhaswamy. „Anti-MRSA activity of aldehyde Schiff base N-aryl thiosemicarbazones“. British Journal of Biomedical Science 66, Nr. 1 (Januar 2009): 14–19. http://dx.doi.org/10.1080/09674845.2009.11730238.
Sawada, Hiromi, Kenji Onoda, Daichi Morita, Erika Ishitsubo, Kenji Matsuno, Hiroaki Tokiwa, Teruo Kuroda und Hiroyuki Miyachi. „Structure–anti-MRSA activity relationship of macrocyclic bis(bibenzyl) derivatives“. Bioorganic & Medicinal Chemistry Letters 23, Nr. 24 (Dezember 2013): 6563–68. http://dx.doi.org/10.1016/j.bmcl.2013.10.069.