Zanamivir (BioDeep_00000006660)

 

Secondary id: BioDeep_00001868183

human metabolite blood metabolite Chemicals and Drugs


代谢物信息卡片


(2R,3R,4S)-4-[(diaminomethylidene)amino]-3-acetamido-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid

化学式: C12H20N4O7 (332.1332)
中文名称: 扎那米韦
谱图信息: 最多检出来源 Homo sapiens(blood) 94.7%

分子结构信息

SMILES: CC(=O)NC1C(C=C(OC1C(C(CO)O)O)C(=O)O)N=C(N)N
InChI: InChI=1S/C12H20N4O7/c1-4(18)15-8-5(16-12(13)14)2-7(11(21)22)23-10(8)9(20)6(19)3-17/h2,5-6,8-10,17,19-20H,3H2,1H3,(H,15,18)(H,21,22)(H4,13,14,16)/t5-,6+,8+,9+,10+/m0/s1

描述信息

Zanamivir is only found in individuals that have used or taken this drug. It is a guanido-neuraminic acid that is used to inhibit neuraminidase. [PubChem]The proposed mechanism of action of zanamivir is via inhibition of influenza virus neuraminidase with the possibility of alteration of virus particle aggregation and release. By binding and inhibiting the neuraminidase protein, the drug renders the influenza virus unable to escape its host cell and infect others.
J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AH - Neuraminidase inhibitors
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents
C254 - Anti-Infective Agent > C281 - Antiviral Agent
D004791 - Enzyme Inhibitors

同义名列表

33 个代谢物同义名

(2R,3R,4S)-4-[(diaminomethylidene)amino]-3-acetamido-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid; (2R,3R,4S)-3-(Acetylamino)-4-carbamimidamido-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid; (2R,3R,4S)-3-(Acetylamino)-4-carbamimidamido-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylate; 5-(Acetylamino)-2,6-anhydro-4-carbamimidamido-3,4,5-trideoxy-D-glycero-D-galacto-non-2-enonic acid; 5-(Acetylamino)-2,6-anhydro-4-carbamimidamido-3,4,5-trideoxy-D-glycero-D-galacto-non-2-enonate; 5-Acetamido-2,6-anhydro-3,4,5-trideoxy-4-guanidino-D-glycero-D-galacto-non-2-enonic acid; 5-Acetamido-2,6-anhydro-3,4,5-trideoxy-4-guanidino-D-glycero-D-galacto-non-2-enonate; 5-Acetylamino-2,6-anhydro-4-guanidino-3,4,5-trideoxy-D-galacto-non-enoic acid; 2,3-Didehydro-2,4-dideoxy-4-guanidino-N-acetyl-D-neuraminic acid; 2,3-Didehydro-2,4-dideoxy-4-guanidinyl-N-acetylneuraminic acid; 4-Guanidino-2,4-dideoxy-2,3-didehydro-N-acetylneuraminic acid; 4-Guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminic acid; Acid, 4-guanidino-2-deoxy-2,3-didehydro-N-acetylneuraminic; 4 Guanidino 2 deoxy 2,3 didehydro N acetylneuraminic acid; 4-Guanidino-2-deoxy-2,3-didehydro-N-acetylneuraminic acid; 4-Guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminate; GlaxoSmithKline brand OF zanamivir; Glaxo wellcome brand OF zanamivir; Zanamivir glaxosmithkline brand; Biota brand OF zanamivir; Zanamivir biota brand; 4 Guanidino neu5ac2En; 4-Guanidino-neu5ac2En; Modified sialic acid; SCHEMBL3497032; Zanamavir; Zanamivir; Relenza; GANA; ZMR; GNA; Zanamivir; Zanamivir



数据库引用编号

22 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 7 ACE2, ANXA4, NEU1, NEU2, NEU3, NEU4, TLR4
Peripheral membrane protein 5 ANXA4, CYP1B1, ERVW-1, NEU1, NEU3
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 3 CALU, CYP1B1, NEU4
Mitochondrion membrane 1 NEU4
Nucleus 1 ANXA4
cytosol 1 NEU2
Cell membrane 5 ACE2, NEU3, TLR4, TNF, TNFRSF1A
Early endosome membrane 1 NEU3
Multi-pass membrane protein 1 SLC15A1
Golgi apparatus membrane 1 TNFRSF1A
cell junction 1 NEU1
cell surface 6 ACE2, ANXA4, TLR4, TNF, TNFRSF1A, TNR
glutamatergic synapse 1 TNR
Golgi apparatus 2 CALU, ST6GAL1
Golgi membrane 2 ST6GAL1, TNFRSF1A
lysosomal membrane 2 NEU1, NEU3
mitochondrial inner membrane 1 NEU4
neuronal cell body 1 TNF
Cytoplasm, cytosol 1 NEU2
Lysosome 4 NEU1, NEU2, NEU3, NEU4
plasma membrane 11 ACE2, ANXA4, ERVW-1, IFNLR1, NEU1, NEU3, NEU4, SLC15A1, TLR4, TNF, TNFRSF1A
Membrane 12 ACE2, ANXA4, CALU, CYP1B1, IFNLR1, NEU1, NEU2, NEU3, NEU4, SLC15A1, TLR4, TNFRSF1A
apical plasma membrane 2 ACE2, SLC15A1
brush border 1 SLC15A1
caveola 1 NEU3
extracellular exosome 3 ACE2, ANXA4, NEU1
Lysosome membrane 2 NEU1, NEU3
Lumenal side 1 NEU1
endoplasmic reticulum 1 CALU
extracellular space 8 ACE2, CXCL8, IFNA1, IL10, IL6, TNF, TNFRSF1A, TNR
lysosomal lumen 2 NEU1, NEU4
perinuclear region of cytoplasm 2 ANXA4, TLR4
Schaffer collateral - CA1 synapse 1 TNR
mitochondrion 1 CYP1B1
intracellular membrane-bounded organelle 2 CYP1B1, NEU1
Microsome membrane 2 CYP1B1, NEU4
Single-pass type I membrane protein 5 ACE2, ERVW-1, IFNLR1, TLR4, TNFRSF1A
Secreted 7 ACE2, CALU, CXCL8, IFNA1, IL10, IL6, TNFRSF1A
extracellular region 10 ACE2, CALU, CXCL8, IL10, IL6, NEU1, ST6GAL1, TNF, TNFRSF1A, TNR
Mitochondrion outer membrane 1 NEU4
mitochondrial outer membrane 1 NEU4
Cell projection, cilium 1 ACE2
nuclear membrane 1 ANXA4
external side of plasma membrane 3 NEU3, TLR4, TNF
Secreted, extracellular space, extracellular matrix 1 TNR
cytoplasmic vesicle 1 ANXA4
Early endosome 1 TLR4
recycling endosome 1 TNF
Single-pass type II membrane protein 2 ST6GAL1, TNF
Apical cell membrane 2 ACE2, SLC15A1
Membrane raft 4 ACE2, TNF, TNFRSF1A, TNR
collagen-containing extracellular matrix 2 ANXA4, TNR
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 2 TLR4, TNFRSF1A
Cell projection, neuron projection 1 NEU4
Zymogen granule membrane 1 ANXA4
neuron projection 1 NEU4
cilium 1 ACE2
phagocytic cup 2 TLR4, TNF
brush border membrane 1 ACE2
Recycling endosome membrane 1 NEU3
Membrane, caveola 1 NEU3
Melanosome 1 CALU
Golgi cisterna membrane 1 ST6GAL1
lipopolysaccharide receptor complex 1 TLR4
endoplasmic reticulum lumen 3 ACE2, CALU, IL6
specific granule lumen 1 NEU1
endocytic vesicle membrane 1 ACE2
Golgi apparatus, Golgi stack membrane 1 ST6GAL1
Lysosome lumen 2 NEU1, NEU4
perineuronal net 1 TNR
vesicle membrane 1 ANXA4
Sarcoplasmic reticulum lumen 1 CALU
[Transmembrane protein]: Cell membrane 1 ERVW-1
[Surface protein]: Cell membrane 1 ERVW-1
[Isoform 1]: Cell membrane 1 NEU4
Golgi medial cisterna 1 ST6GAL1
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalytic complex 1 NEU2
interleukin-6 receptor complex 1 IL6
Golgi trans cisterna 1 ST6GAL1
tumor necrosis factor receptor superfamily complex 1 TNFRSF1A
tenascin complex 1 TNR
[Isoform 2]: Mitochondrion inner membrane 1 NEU4
interleukin-28 receptor complex 1 IFNLR1
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
organelle inner membrane 1 NEU4
[Processed angiotensin-converting enzyme 2]: Secreted 1 ACE2
[Isoform 2]: Apical cell membrane 1 ACE2
[Syncytin-1]: Virion 1 ERVW-1


文献列表

  • Jie Wang-Jairaj, Irene Miller, Aditya Joshi, Tharaka Jayabalan, Amanda Peppercorn, Peter Zammit-Tabona, Amanda Oliver. Zanamivir aqueous solution in severe influenza: A global Compassionate Use Program, 2009-2019. Influenza and other respiratory viruses. 2022 05; 16(3):542-551. doi: 10.1111/irv.12947. [PMID: 34939702]
  • Han Ju, N Arul Murugan, Lingxin Hou, Ping Li, Laura Guizzo, Ying Zhang, Chiara Bertagnin, Xiujie Kong, Dongwei Kang, Ruifang Jia, Xiuli Ma, Ruikun Du, Vasanthanathan Poongavanam, Arianna Loregian, Bing Huang, Xinyong Liu, Peng Zhan. Identification of C5-NH2 Modified Oseltamivir Derivatives as Novel Influenza Neuraminidase Inhibitors with Highly Improved Antiviral Activities and Favorable Druggability. Journal of medicinal chemistry. 2021 12; 64(24):17992-18009. doi: 10.1021/acs.jmedchem.1c01366. [PMID: 34735766]
  • Xun Lv, Pengfei Wang, Chenning Li, Shuihong Cheng, Yuhai Bi, Xuebing Li. Zanamivir-Cholesterol Conjugate: A Long-Acting Neuraminidase Inhibitor with Potent Efficacy against Drug-Resistant Influenza Viruses. Journal of medicinal chemistry. 2021 12; 64(23):17403-17412. doi: 10.1021/acs.jmedchem.1c01531. [PMID: 34797984]
  • Xin Liu, Weichuan Luo, Boning Zhang, Yong Gu Lee, Imrul Shahriar, Madduri Srinivasarao, Philip S Low. Design of Neuraminidase-Targeted Imaging and Therapeutic Agents for the Diagnosis and Treatment of Influenza Virus Infections. Bioconjugate chemistry. 2021 08; 32(8):1548-1553. doi: 10.1021/acs.bioconjchem.1c00255. [PMID: 34161726]
  • Bettina Sehnert, Juliane Mietz, Rita Rzepka, Stefanie Buchholz, Andrea Maul-Pavicic, Sandra Schaffer, Falk Nimmerjahn, Reinhard E Voll. Neuraminidase Inhibitor Zanamivir Ameliorates Collagen-Induced Arthritis. International journal of molecular sciences. 2021 Jan; 22(3):. doi: 10.3390/ijms22031428. [PMID: 33572654]
  • Liqian Zhou, Juanjuan Wang, Guangyi Liu, Qingqing Lu, Ruyi Dong, Geng Tian, Jialiang Yang, Lihong Peng. Probing antiviral drugs against SARS-CoV-2 through virus-drug association prediction based on the KATZ method. Genomics. 2020 11; 112(6):4427-4434. doi: 10.1016/j.ygeno.2020.07.044. [PMID: 32745502]
  • Liva Checkmahomed, Blandine Padey, Andrés Pizzorno, Olivier Terrier, Manuel Rosa-Calatrava, Yacine Abed, Mariana Baz, Guy Boivin. In Vitro Combinations of Baloxavir Acid and Other Inhibitors against Seasonal Influenza A Viruses. Viruses. 2020 10; 12(10):. doi: 10.3390/v12101139. [PMID: 33049959]
  • Chuanxiong Nie, Badri Parshad, Sumati Bhatia, Chong Cheng, Marlena Stadtmüller, Alexander Oehrl, Yannic Kerkhoff, Thorsten Wolff, Rainer Haag. Topology-Matching Design of an Influenza-Neutralizing Spiky Nanoparticle-Based Inhibitor with a Dual Mode of Action. Angewandte Chemie (International ed. in English). 2020 09; 59(36):15532-15536. doi: 10.1002/anie.202004832. [PMID: 32421225]
  • Donald C Hall, Hai-Feng Ji. A search for medications to treat COVID-19 via in silico molecular docking models of the SARS-CoV-2 spike glycoprotein and 3CL protease. Travel medicine and infectious disease. 2020 May; 35(?):101646. doi: 10.1016/j.tmaid.2020.101646. [PMID: 32294562]
  • Natalia A Ilyushina, Takashi E Komatsu, William L Ince, Eric F Donaldson, Nicolette Lee, Julian J O'Rear, Raymond P Donnelly. Influenza A virus hemagglutinin mutations associated with use of neuraminidase inhibitors correlate with decreased inhibition by anti-influenza antibodies. Virology journal. 2019 11; 16(1):149. doi: 10.1186/s12985-019-1258-x. [PMID: 31783761]
  • Takanori Tomozawa, Kazuki Hoshino, Makoto Yamashita, Shuku Kubo. Efficacy of laninamivir octanoate in mice with advanced inflammation stage caused by infection of highly lethal influenza virus. Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy. 2019 Aug; 25(8):584-588. doi: 10.1016/j.jiac.2019.02.023. [PMID: 30935767]
  • R Farrukee, J Butler, P C Reading, A C Hurt. Characterization of substitutions in the neuraminidase of A(H7N9) influenza viruses selected following serial passage in the presence of different neuraminidase inhibitors. Antiviral research. 2019 08; 168(?):68-75. doi: 10.1016/j.antiviral.2019.05.009. [PMID: 31132385]
  • Jing Tang, Jing Zhang, Jianfang Zhou, Wenfei Zhu, Lei Yang, Shumei Zou, Hejiang Wei, Li Xin, Weijuan Huang, Xiyan Li, Yanhui Cheng, Dayan Wang. Highly pathogenic avian influenza H7N9 viruses with reduced susceptibility to neuraminidase inhibitors showed comparable replication capacity to their sensitive counterparts. Virology journal. 2019 07; 16(1):87. doi: 10.1186/s12985-019-1194-9. [PMID: 31266524]
  • Merryn Roe, Matthew Kaye, Pina Iannello, Hilda Lau, Iwona Buettner, M Ximena Tolosa, Tasoula Zakis, Vivian K Leung, Michelle K Chow. Report on influenza viruses received and tested by the Melbourne WHO Collaborating Centre for Reference and Research on Influenza in 2017. Communicable diseases intelligence (2018). 2019 Jun; 43(?):. doi: . [PMID: 31203585]
  • Khristine Kaith S Lloren, Jin Jung Kwon, Won-Suk Choi, Ju Hwan Jeong, Su Jeong Ahn, Young Ki Choi, Yun Hee Baek, Min-Suk Song. In Vitro and In Vivo Characterization of Novel Neuraminidase Substitutions in Influenza A(H1N1)pdm09 Virus Identified Using Laninamivir-Mediated In Vitro Selection. Journal of virology. 2019 03; 93(6):. doi: 10.1128/jvi.01825-18. [PMID: 30602610]
  • Matthias Müller, Daniel Lauster, Helen H K Wildenauer, Andreas Herrmann, Stephan Block. Mobility-Based Quantification of Multivalent Virus-Receptor Interactions: New Insights Into Influenza A Virus Binding Mode. Nano letters. 2019 03; 19(3):1875-1882. doi: 10.1021/acs.nanolett.8b04969. [PMID: 30719917]
  • Jian Zhang, Natarajan Arul Murugan, Ye Tian, Chiara Bertagnin, Zengjun Fang, Dongwei Kang, Xiujie Kong, Haiyong Jia, Zhuosen Sun, Ruifang Jia, Ping Gao, Vasanthanathan Poongavanam, Arianna Loregian, Wenfang Xu, Xiuli Ma, Xiao Ding, Bing Huang, Peng Zhan, Xinyong Liu. Structure-Based Optimization of N-Substituted Oseltamivir Derivatives as Potent Anti-Influenza A Virus Agents with Significantly Improved Potency against Oseltamivir-Resistant N1-H274Y Variant. Journal of medicinal chemistry. 2018 11; 61(22):9976-9999. doi: 10.1021/acs.jmedchem.8b01065. [PMID: 30365885]
  • Hou-Wen Cheng, Hsiao-Wen Wang, Tsung-Yun Wong, Hsien-Wei Yeh, Yi-Chun Chen, Der-Zen Liu, Pi-Hui Liang. Synthesis of S-linked NeuAc-α(2-6)-di-LacNAc bearing liposomes for H1N1 influenza virus inhibition assays. Bioorganic & medicinal chemistry. 2018 05; 26(9):2262-2270. doi: 10.1016/j.bmc.2018.02.012. [PMID: 29472127]
  • Ramona Trebbien, Claus Bohn Christiansen, Thea Kølsen Fischer. Antiviral resistance due to deletion in the neuraminidase gene and defective interfering-like viral polymerase basic 2 RNA of influenza A virus subtype H3N2. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2018 05; 102(?):1-6. doi: 10.1016/j.jcv.2018.02.005. [PMID: 29448067]
  • Almiro Tivane, Rodney Daniels, Neuza Nguenha, Loira Machalele, Afonso Nacoto, Mirela Pale, Edirsse Mateonane, Sandra Mavale, Josina Chilundo, Délcio Muteto, Judite Salência, Félix Albati, Eduardo Gudo, Tufária Mussá, John McCauley. Antigenic and genetic characterization of influenza viruses isolated in Mozambique during the 2015 season. PloS one. 2018; 13(7):e0201248. doi: 10.1371/journal.pone.0201248. [PMID: 30048502]
  • Won-Suk Choi, Ju Hwan Jeong, Jin Jung Kwon, Su Jeong Ahn, Khristine Kaith S Lloren, Hyeok-Il Kwon, Hee Bok Chae, Jungwon Hwang, Myung Hee Kim, Chul-Joong Kim, Richard J Webby, Elena A Govorkova, Young Ki Choi, Yun Hee Baek, Min-Suk Song. Screening for Neuraminidase Inhibitor Resistance Markers among Avian Influenza Viruses of the N4, N5, N6, and N8 Neuraminidase Subtypes. Journal of virology. 2018 01; 92(1):. doi: 10.1128/jvi.01580-17. [PMID: 29046464]
  • Kaoru Toyama, Hidetoshi Furuie, Hitoshi Ishizuka. Intrapulmonary Pharmacokinetics of Laninamivir, a Neuraminidase Inhibitor, after a Single Nebulized Administration of Laninamivir Octanoate in Healthy Japanese Subjects. Antimicrobial agents and chemotherapy. 2018 01; 62(1):. doi: 10.1128/aac.01722-17. [PMID: 29061751]
  • Mitsuru Tsuji, Nongluk Sriwilaijaroen, Hideo Inoue, Kazuhiko Miki, Kaoru Kinoshita, Kiyotaka Koyama, Kimio Furuhata, Yasuo Suzuki, Kunio Takahashi. Synthesis and anti-influenza virus evaluation of triterpene-sialic acid conjugates. Bioorganic & medicinal chemistry. 2018 01; 26(1):17-24. doi: 10.1016/j.bmc.2017.09.038. [PMID: 29198893]
  • Junhyung Cho, Hwajung Yi, Eun Young Jang, Mi-Seon Lee, Joo-Yeon Lee, Chun Kang, Chan Hee Lee, Kisoon Kim. Mycophenolic mofetil, an alternative antiviral and immunomodulator for the highly pathogenic avian influenza H5N1 virus infection. Biochemical and biophysical research communications. 2017 12; 494(1-2):298-304. doi: 10.1016/j.bbrc.2017.10.037. [PMID: 29017920]
  • Stefanie Quosdorf, Anja Schuetz, Herbert Kolodziej. Different Inhibitory Potencies of Oseltamivir Carboxylate, Zanamivir, and Several Tannins on Bacterial and Viral Neuraminidases as Assessed in a Cell-Free Fluorescence-Based Enzyme Inhibition Assay. Molecules (Basel, Switzerland). 2017 Nov; 22(11):. doi: 10.3390/molecules22111989. [PMID: 29149072]
  • Abraham Ochoa, Enrique Álvarez-Bohórquez, Eduardo Castillero, Luis F Olguin. Detection of Enzyme Inhibitors in Crude Natural Extracts Using Droplet-Based Microfluidics Coupled to HPLC. Analytical chemistry. 2017 05; 89(9):4889-4896. doi: 10.1021/acs.analchem.6b04988. [PMID: 28374582]
  • Takashi Azuma, Mao Ishida, Kanae Hisamatsu, Ayami Yunoki, Kana Otomo, Mari Kunitou, Mai Shimizu, Kaori Hosomaru, Shiori Mikata, Yoshiki Mino. Fate of new three anti-influenza drugs and one prodrug in the water environment. Chemosphere. 2017 Feb; 169(?):550-557. doi: 10.1016/j.chemosphere.2016.11.102. [PMID: 27898328]
  • Ramona Trebbien, Svend Stenvang Pedersen, Kristine Vorborg, Kristina Træholt Franck, Thea Kølsen Fischer. Development of oseltamivir and zanamivir resistance in influenza A(H1N1)pdm09 virus, Denmark, 2014. Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2017 Jan; 22(3):. doi: 10.2807/1560-7917.es.2017.22.3.30445. [PMID: 28128091]
  • Anja Hoffmann, Dennis Schade, Johannes Kirchmair, Bernd Clement, Andreas Sauerbrei, Michaela Schmidtke. Platform for determining the inhibition profile of neuraminidase inhibitors in an influenza virus N1 background. Journal of virological methods. 2016 11; 237(?):192-199. doi: 10.1016/j.jviromet.2016.09.014. [PMID: 27659246]
  • Lifeng Fu, Yuhai Bi, Yan Wu, Shanshan Zhang, Jianxun Qi, Yan Li, Xuancheng Lu, Zhenning Zhang, Xun Lv, Jinghua Yan, George F Gao, Xuebing Li. Structure-Based Tetravalent Zanamivir with Potent Inhibitory Activity against Drug-Resistant Influenza Viruses. Journal of medicinal chemistry. 2016 07; 59(13):6303-12. doi: 10.1021/acs.jmedchem.6b00537. [PMID: 27341624]
  • Nongluk Sriwilaijaroen, Sadagopan Magesh, Akihiro Imamura, Hiromune Ando, Hideharu Ishida, Miho Sakai, Erika Ishitsubo, Takanori Hori, Setsuko Moriya, Takeshi Ishikawa, Kazuo Kuwata, Takato Odagiri, Masato Tashiro, Hiroaki Hiramatsu, Kenji Tsukamoto, Taeko Miyagi, Hiroaki Tokiwa, Makoto Kiso, Yasuo Suzuki. A Novel Potent and Highly Specific Inhibitor against Influenza Viral N1-N9 Neuraminidases: Insight into Neuraminidase-Inhibitor Interactions. Journal of medicinal chemistry. 2016 05; 59(10):4563-77. doi: 10.1021/acs.jmedchem.5b01863. [PMID: 27095056]
  • Benjamin Bailly, Larissa Dirr, Ibrahim M El-Deeb, Ralf Altmeyer, Patrice Guillon, Mark von Itzstein. A dual drug regimen synergistically blocks human parainfluenza virus infection. Scientific reports. 2016 Apr; 6(?):24138. doi: 10.1038/srep24138. [PMID: 27053240]
  • Ahmed M Tolah, Esam I Azhar, Anwar M Hashem. Susceptibility of influenza viruses circulating in Western Saudi Arabia to neuraminidase inhibitors. Saudi medical journal. 2016 Apr; 37(4):461-5. doi: 10.15537/smj.2016.4.14837. [PMID: 27052292]
  • Siriwan Charyasriwong, Takahiro Haruyama, Nobuyuki Kobayashi. In vitro evaluation of the antiviral activity of methylglyoxal against influenza B virus infection. Drug discoveries & therapeutics. 2016 ; 10(4):201-10. doi: 10.5582/ddt.2016.01045. [PMID: 27558282]
  • Naoko Ito, Masatoki Sato, Nobuo Momoi, Yoshimichi Aoyagi, Kisei Endo, Mina Chishiki, Yukihiko Kawasaki, Mitsuaki Hosoya. Influenza A H1N1 pdm09-associated myocarditis during zanamivir therapy. Pediatrics international : official journal of the Japan Pediatric Society. 2015 Dec; 57(6):1172-4. doi: 10.1111/ped.12712. [PMID: 26482326]
  • Dennis Schade, Jürke Kotthaus, Lukas Riebling, Joscha Kotthaus, Helge Müller-Fielitz, Walter Raasch, Anja Hoffmann, Michaela Schmidtke, Bernd Clement. Zanamivir Amidoxime- and N-Hydroxyguanidine-Based Prodrug Approaches to Tackle Poor Oral Bioavailability. Journal of pharmaceutical sciences. 2015 Sep; 104(9):3208-19. doi: 10.1002/jps.24508. [PMID: 26037932]
  • Byung Soon Hwang, In-Kyoung Lee, Hwa Jung Choi, Bong-Sik Yun. Anti-influenza activities of polyphenols from the medicinal mushroom Phellinus baumii. Bioorganic & medicinal chemistry letters. 2015 Aug; 25(16):3256-60. doi: 10.1016/j.bmcl.2015.05.081. [PMID: 26077494]
  • Tatiana Baranovich, Justin Bahl, Bindumadhav M Marathe, Marie Culhane, Evelyn Stigger-Rosser, Daniel Darnell, Bryan S Kaplan, James F Lowe, Richard J Webby, Elena A Govorkova. Influenza A viruses of swine circulating in the United States during 2009-2014 are susceptible to neuraminidase inhibitors but show lineage-dependent resistance to adamantanes. Antiviral research. 2015 May; 117(?):10-9. doi: 10.1016/j.antiviral.2015.02.004. [PMID: 25701593]
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