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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1186/s40169-017-0181-2.

Title:
A perspective on multi-target drug discovery and design for complex diseases | Clinical and Translational Medicine
Description:
Diseases of infection, of neurodegeneration (such as Alzheimer’s and Parkinson’s diseases), and of malignancy (cancers) have complex and varied causative factors. Modern drug discovery has the power to identify potential modulators for multiple targets from millions of compounds. Computational approaches allow the determination of the association of each compound with its target before chemical synthesis and biological testing is done. These approaches depend on the prior identification of clinically and biologically validated targets. This Perspective will focus on the molecular and computational approaches that underpin drug design by medicinal chemists to promote understanding and collaboration with clinical scientists.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We don't see any clear sign of profit-making.

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

google, scholar, pubmed, article, drug, cas, drugs, compounds, multitarget, discovery, molecular, design, target, targets, chem, activity, receptor, ligands, med, treatment, screening, docking, receptors, binding, cns, computational, development, approved, central, diseases, chemical, disease, virtual, inhibitors, methods, brain, approaches, approach, biological, lead, effects, molecules, inhibitor, ligand, multiple, identification, analysis, alzheimers, potential, combination,

Topics {✒️}

β1-adrenergic g-protein-coupled receptor n-methyl-d-aspartate glutamate receptors methyl]-n-methylprop-2-yn-1-amine hybrids bautista-aguilera om dopamine d-3 receptor-preferring article download pdf protein-coupled receptor database n-methylprop-2-yn-1-amine serotonin-dopamine activity modulator ns3/4a protease inhibitor nonsteroidal anti-inflammatory drugs multi-kinase inhibitors emerged structure-based virtual screening pathway-target-drug-disease relationships athletic performance-enhancing substances predicting p-glycoprotein efflux extending cell-based assays pan-kinase inhibitor staurosporine multipotent tacrine-dihydropyridine hybrids pharmacophore-based virtual screening cheminformatics-based target identification ligand-based virtual screening p-glycoprotein efflux properties small-scale academic laboratories quantitative structure-exposure relationships central nervous system sg/group/ttd/ttd 1-methyl-1h-indol-2-yl multi-target drugs emerge predicting multi-target bioactivities central beta-amyloid computer-aided drug discovery quantitative structure–activity relationship n-substituted piperidin-4-yl multi-target ligands intended structure-brain exposure relationships docked ligand-target complexes radioiodine-refractory thyroid cancers designing multi-target drugs structure-based drug discovery anti-cancer drug discovery multi-target-directed ligands including pan-cdks inhibitors multi-target drug discovery model gene-environment interactions grid-based molecular docking pharmacophore-based docking program post-synaptic d2 receptors targeting cyclin-dependent kinases previous 3d-qsar analyses

Questions {❓}

  • Cherkasov A, Muratov EN, Fourches D, Varnek A, Baskin II, Cronin M et al (2014) QSAR modeling: where have you been?
  • Hughes RE, Nikolic K, Ramsay RR (2016) One for all?
  • Peters JU (2013) Polypharmacology—foe or friend?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:A perspective on multi-target drug discovery and design for complex diseases
         description:Diseases of infection, of neurodegeneration (such as Alzheimer’s and Parkinson’s diseases), and of malignancy (cancers) have complex and varied causative factors. Modern drug discovery has the power to identify potential modulators for multiple targets from millions of compounds. Computational approaches allow the determination of the association of each compound with its target before chemical synthesis and biological testing is done. These approaches depend on the prior identification of clinically and biologically validated targets. This Perspective will focus on the molecular and computational approaches that underpin drug design by medicinal chemists to promote understanding and collaboration with clinical scientists.
         datePublished:2018-01-17T00:00:00Z
         dateModified:2018-01-17T00:00:00Z
         pageStart:1
         pageEnd:14
         license:http://creativecommons.org/licenses/by/4.0/
         sameAs:https://doi.org/10.1186/s40169-017-0181-2
         keywords:
            Multi-target drugs
            Neurodegeneration
            Cancer
            Cheminformatics
            Virtual screening
            Biological assays
            Medicine/Public Health
            general
         image:
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         isPartOf:
            name:Clinical and Translational Medicine
            issn:
               2001-1326
            volumeNumber:7
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               name:Rona R. Ramsay
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                     address:
                        name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
                        type:PostalAddress
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               name:Katarina Nikolic
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                     name:University of Belgrade
                     address:
                        name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
                        type:PostalAddress
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      headline:A perspective on multi-target drug discovery and design for complex diseases
      description:Diseases of infection, of neurodegeneration (such as Alzheimer’s and Parkinson’s diseases), and of malignancy (cancers) have complex and varied causative factors. Modern drug discovery has the power to identify potential modulators for multiple targets from millions of compounds. Computational approaches allow the determination of the association of each compound with its target before chemical synthesis and biological testing is done. These approaches depend on the prior identification of clinically and biologically validated targets. This Perspective will focus on the molecular and computational approaches that underpin drug design by medicinal chemists to promote understanding and collaboration with clinical scientists.
      datePublished:2018-01-17T00:00:00Z
      dateModified:2018-01-17T00:00:00Z
      pageStart:1
      pageEnd:14
      license:http://creativecommons.org/licenses/by/4.0/
      sameAs:https://doi.org/10.1186/s40169-017-0181-2
      keywords:
         Multi-target drugs
         Neurodegeneration
         Cancer
         Cheminformatics
         Virtual screening
         Biological assays
         Medicine/Public Health
         general
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs40169-017-0181-2/MediaObjects/40169_2017_181_Fig1_HTML.gif
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         name:Clinical and Translational Medicine
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            2001-1326
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         name:Springer Berlin Heidelberg
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            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
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            name:Rona R. Ramsay
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                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Marija R. Popovic-Nikolic
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                  name:University of Belgrade
                  address:
                     name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
                     type:PostalAddress
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            name:Katarina Nikolic
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                  name:University of Belgrade
                  address:
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                     type:PostalAddress
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                  name:Alma Mater Studiorum-Bologna University
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                     name:Department of Pharmacy and Biotechnology, Alma Mater Studiorum-Bologna University, Bologna, Italy
                     type:PostalAddress
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         name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
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         name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
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            name:Biomedical Sciences Research Complex, University of St Andrews
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               name:Biomedical Sciences Research Complex, University of St Andrews, St Andrews, UK
               type:PostalAddress
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      affiliation:
            name:University of Belgrade
            address:
               name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
               type:PostalAddress
            type:Organization
      name:Katarina Nikolic
      affiliation:
            name:University of Belgrade
            address:
               name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
               type:PostalAddress
            type:Organization
      name:Elisa Uliassi
      affiliation:
            name:Alma Mater Studiorum-Bologna University
            address:
               name:Department of Pharmacy and Biotechnology, Alma Mater Studiorum-Bologna University, Bologna, Italy
               type:PostalAddress
            type:Organization
      name:Maria Laura Bolognesi
      affiliation:
            name:Alma Mater Studiorum-Bologna University
            address:
               name:Department of Pharmacy and Biotechnology, Alma Mater Studiorum-Bologna University, Bologna, Italy
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Biomedical Sciences Research Complex, University of St Andrews, St Andrews, UK
      name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
      name:Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia
      name:Department of Pharmacy and Biotechnology, Alma Mater Studiorum-Bologna University, Bologna, Italy
      name:Department of Pharmacy and Biotechnology, Alma Mater Studiorum-Bologna University, Bologna, Italy

External Links {🔗}(337)

Analytics and Tracking {📊}

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Libraries {📚}

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5.34s.