Comparing the Suitability of Autodock, Gold and Glide for the Docking and Predicting the Possible Targets of Ru(II)-Based Complexes as Anticancer Agents
出版年份 2013 全文链接
标题
Comparing the Suitability of Autodock, Gold and Glide for the Docking and Predicting the Possible Targets of Ru(II)-Based Complexes as Anticancer Agents
作者
关键词
-
出版物
MOLECULES
Volume 18, Issue 4, Pages 3760-3778
出版商
MDPI AG
发表日期
2013-03-26
DOI
10.3390/molecules18043760
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Inhibitory activities and possible anticancer targets of Ru(II)-based complexes using computational docking method
- (2012) Adebayo A. Adeniyi et al. JOURNAL OF MOLECULAR GRAPHICS & MODELLING
- In silico screening of quadruplex-binding ligands
- (2012) Dik-Lung Ma et al. METHODS
- A Ruthenium Antimetastasis Agent Forms Specific Histone Protein Adducts in the Nucleosome Core
- (2011) Bin Wu et al. CHEMISTRY-A EUROPEAN JOURNAL
- Metal-based antitumour drugs in the post-genomic era: what comes next?
- (2011) Gianni Sava et al. DALTON TRANSACTIONS
- Conjugation of Organoruthenium(II) 3-(1H-Benzimidazol-2-yl)pyrazolo[3,4-b]pyridines and Indolo[3,2-d]benzazepines to Recombinant Human Serum Albumin: a Strategy To Enhance Cytotoxicity in Cancer Cells
- (2011) Iryna N. Stepanenko et al. INORGANIC CHEMISTRY
- A QM/MM study of the binding of RAPTA ligands to cathepsin B
- (2011) Antonella Ciancetta et al. JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN
- uPAR and cathepsin B downregulation induces apoptosis by targeting calcineurin A to BAD via Bcl-2 in glioma
- (2011) Rama Rao Malla et al. JOURNAL OF NEURO-ONCOLOGY
- First Ruthenium Organometallic Complex of Antibacterial Agent Ofloxacin. Crystal Structure and Interactions with DNA
- (2010) Iztok Turel et al. INORGANIC CHEMISTRY
- Is the Reactivity of M(II)−Arene Complexes of 3-Hydroxy-2(1H)-pyridones to Biomolecules the Anticancer Activity Determining Parameter?
- (2010) Muhammad Hanif et al. INORGANIC CHEMISTRY
- Intracellular protein binding patterns of the anticancer ruthenium drugs KP1019 and KP1339
- (2010) Petra Heffeter et al. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
- Metabolization of [Ru(η6-C6H5CF3)(pta)Cl2]: a cytotoxic RAPTA-type complex with a strongly electron withdrawing arene ligand
- (2010) Alexander E. Egger et al. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
- Organometallic Anticancer Compounds
- (2010) Gilles Gasser et al. JOURNAL OF MEDICINAL CHEMISTRY
- Mononuclear transition metal complexes with sterically hindered carboxylate ligands: Synthesis, structural and spectral properties
- (2010) Sethuraman Kannan et al. POLYHEDRON
- The Crystal Structure of BRAF in Complex with an Organoruthenium Inhibitor Reveals a Mechanism for Inhibition of an Active Form of BRAF Kinase
- (2009) Peng Xie et al. BIOCHEMISTRY
- Arene Control over Thiolate to Sulfinate Oxidation in Albumin by Organometallic Ruthenium Anticancer Complexes
- (2009) Wenbing Hu et al. CHEMISTRY-A EUROPEAN JOURNAL
- AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility
- (2009) Garrett M. Morris et al. JOURNAL OF COMPUTATIONAL CHEMISTRY
- KP1019, A New Redox-Active Anticancer Agent - Preclinical Development and Results of a Clinical Phase I Study in Tumor Patients
- (2008) Christian G. Hartinger et al. CHEMISTRY & BIODIVERSITY
- Polymorphisms of Thymidylate Synthase in the 5′- and 3′-Untranslated Regions and Gastric Cancer
- (2008) Wen Zhuang et al. DIGESTIVE DISEASES AND SCIENCES
- The ruthenium(II)–arene compound RAPTA-C induces apoptosis in EAC cells through mitochondrial and p53–JNK pathways
- (2008) Soumya Chatterjee et al. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
- Emerging Protein Targets for Anticancer Metallodrugs: Inhibition of Thioredoxin Reductase and Cathepsin B by Antitumor Ruthenium(II)−Arene Compounds
- (2008) Angela Casini et al. JOURNAL OF MEDICINAL CHEMISTRY
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