Example of Drug Discovery Today format
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Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format
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Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format Example of Drug Discovery Today format
Sample paper formatted on SciSpace - SciSpace
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open access Open Access ISSN: 13596446 e-ISSN: 18785832
recommended Recommended

Drug Discovery Today — Template for authors

Publisher: Elsevier
Categories Rank Trend in last 3 yrs
Pharmacology #9 of 297 up up by 1 rank
Drug Discovery #6 of 145 down down by 1 rank
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 712 Published Papers | 10073 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 10/07/2020
Insights & related journals
General info
Top papers
Popular templates
Get started guide
Why choose from SciSpace
FAQ

Journal Performance & Insights

  • Impact Factor
  • CiteRatio
  • SJR
  • SNIP

Impact factor determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

7.321

6% from 2018

Impact factor for Drug Discovery Today from 2016 - 2019
Year Value
2019 7.321
2018 6.88
2017 6.848
2016 6.369
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 6% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

CiteRatio is a measure of average citations received per peer-reviewed paper published in the journal.

14.1

10% from 2019

CiteRatio for Drug Discovery Today from 2016 - 2020
Year Value
2020 14.1
2019 12.8
2018 13.6
2017 12.3
2016 11.4
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 10% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR) measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

1.778

6% from 2019

SJR for Drug Discovery Today from 2016 - 2020
Year Value
2020 1.778
2019 1.896
2018 2.248
2017 2.008
2016 2.17
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 6% in last years.
  • This journal’s SJR is in the top 10 percentile category.

Source Normalized Impact per Paper (SNIP) measures actual citations received relative to citations expected for the journal's category.

2.084

14% from 2019

SNIP for Drug Discovery Today from 2016 - 2020
Year Value
2020 2.084
2019 1.832
2018 1.988
2017 1.624
2016 1.887
graph view Graph view
table view Table view

insights Insights

  • SNIP of this journal has increased by 14% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

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open access Open Access ISSN: 1633864 e-ISSN: 15206025
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CiteRatio: 6.5 | SJR: 0.976 | SNIP: 1.593
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Drug Discovery Today

Guideline source: View

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Elsevier

Drug Discovery Today

Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingl...... Read More

Pharmacology

Drug Discovery

Pharmacology, Toxicology and Pharmaceutics

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Last updated on
10 Jul 2020
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ISSN
1359-6446
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Impact Factor
High - 1.794
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
elsarticle-num
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Citation Type
Numbered
[25]
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Bibliography Example
G. E. Blonder, M. Tinkham, T. M. Klapwijk, Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion, Phys. Rev. B 25 (7) (1982) 4515–4532. URL 10.1103/PhysRevB.25.4515

Top papers written in this journal

Journal Article DOI: 10.1016/S1359-6446(03)02933-7
The growing impact of click chemistry on drug discovery.
Hartmuth C. Kolb1, K. Barry Sharpless1
15 Dec 2003 - Drug Discovery Today

Abstract:

Click chemistry is a modular approach that uses only the most practical and reliable chemical transformations. Its applications are increasingly found in all aspects of drug discovery, ranging from lead finding through combinatorial chemistry and target-templated in situ chemistry, to proteomics and DNA research, using biocon... Click chemistry is a modular approach that uses only the most practical and reliable chemical transformations. Its applications are increasingly found in all aspects of drug discovery, ranging from lead finding through combinatorial chemistry and target-templated in situ chemistry, to proteomics and DNA research, using bioconjugation reactions. The copper-(I)-catalyzed 1,2,3-triazole formation from azides and terminal acetylenes is a particularly powerful linking reaction, due to its high degree of dependability, complete specificity, and the bio-compatibility of the reactants. The triazole products are more than just passive linkers; they readily associate with biological targets, through hydrogen bonding and dipole interactions. read more read less

Topics:

Click chemistry (59%)59% related to the paper, Chemical biology (51%)51% related to the paper
View PDF
2,722 Citations
Journal Article DOI: 10.1016/S1359-6446(05)03575-0
PEGylation, successful approach to drug delivery.
Francesco M. Veronese1, Gianfranco Pasut1
01 Nov 2005 - Drug Discovery Today

Abstract:

PEGylation defines the modification of a protein, peptide or non-peptide molecule by the linking of one or more polyethylene glycol (PEG) chains. This polymer is non-toxic, non-immunogenic, non-antigenic, highly soluble in water and FDA approved. The PEG-drug conjugates have several advantages: a prolonged residence in body, ... PEGylation defines the modification of a protein, peptide or non-peptide molecule by the linking of one or more polyethylene glycol (PEG) chains. This polymer is non-toxic, non-immunogenic, non-antigenic, highly soluble in water and FDA approved. The PEG-drug conjugates have several advantages: a prolonged residence in body, a decreased degradation by metabolic enzymes and a reduction or elimination of protein immunogenicity. Thanks to these favorable properties, PEGylation now plays an important role in drug delivery, enhancing the potentials of peptides and proteins as therapeutic agents. read more read less

Topics:

PEGylation (72%)72% related to the paper, Drug delivery (57%)57% related to the paper, Drug carrier (52%)52% related to the paper
View PDF
1,964 Citations
open accessOpen access Journal Article DOI: 10.1016/J.DRUDIS.2014.10.003
Peptide therapeutics: current status and future directions.
01 Jan 2015 - Drug Discovery Today

Abstract:

Peptides are recognized for being highly selective and efficacious and, at the same time, relatively safe and well tolerated. Consequently, there is an increased interest in peptides in pharmaceutical research and development (R&D), and approximately 140 peptide therapeutics are currently being evaluated in clinical trials. G... Peptides are recognized for being highly selective and efficacious and, at the same time, relatively safe and well tolerated. Consequently, there is an increased interest in peptides in pharmaceutical research and development (R&D), and approximately 140 peptide therapeutics are currently being evaluated in clinical trials. Given that the low-hanging fruits in the form of obvious peptide targets have already been picked, it has now become necessary to explore new routes beyond traditional peptide design. Examples of such approaches are multifunctional and cell penetrating peptides, as well as peptide drug conjugates. Here, we discuss the current status, strengths, and weaknesses of peptides as medicines and the emerging new opportunities in peptide drug design and development. read more read less
View PDF
1,669 Citations
Journal Article DOI: 10.1016/J.DRUDIS.2006.07.005
Exploiting the enhanced permeability and retention effect for tumor targeting.
Arun K. Iyer1, Greish Khaled2, Jun Fang1, Hiroshi Maeda1
01 Sep 2006 - Drug Discovery Today

Abstract:

Of the tumor targeting strategies, the enhanced permeability and retention (EPR) effect of macromolecules is a key mechanism for solid tumor targeting, and considered a gold standard for novel drug design. In this review, we discuss various endogenous factors that can positively impact the EPR effect in tumor tissues. Further... Of the tumor targeting strategies, the enhanced permeability and retention (EPR) effect of macromolecules is a key mechanism for solid tumor targeting, and considered a gold standard for novel drug design. In this review, we discuss various endogenous factors that can positively impact the EPR effect in tumor tissues. Further, we discuss ways to augment the EPR effect by use of exogenous agents, as well as practical methods available in the clinical setting. Some innovative examples developed by researchers to combat cancer by the EPR mechanism are also discussed. read more read less

Topics:

Enhanced permeability and retention effect (63%)63% related to the paper
1,558 Citations
Journal Article DOI: 10.1016/S1359-6446(04)03069-7
Ligand efficiency: a useful metric for lead selection.
15 May 2004 - Drug Discovery Today

Topics:

Ligand efficiency (66%)66% related to the paper, Metric (mathematics) (56%)56% related to the paper, Selection (genetic algorithm) (51%)51% related to the paper
1,529 Citations
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SciSpace is a very innovative solution to the formatting problem and existing providers, such as Mendeley or Word did not really evolve in recent years.

- Andreas Frutiger, Researcher, ETH Zurich, Institute for Biomedical Engineering

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What to expect from SciSpace?

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With SciSpace, you do not need a word template for Drug Discovery Today.

It automatically formats your research paper to Elsevier formatting guidelines and citation style.

You can download a submission ready research paper in pdf, LaTeX and docx formats.

Time comparison

Time taken to format a paper and Compliance with guidelines

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Drug Discovery Today format uses elsarticle-num citation style.

Automatically format and order your citations and bibliography in a click.

SciSpace allows imports from all reference managers like Mendeley, Zotero, Endnote, Google Scholar etc.

Frequently asked questions

Absolutely not! With our tool, you can freely write without having to focus on LaTeX. You can write your entire paper as per the Drug Discovery Today guidelines and autoformat it.

Yes. The template is fully compliant as per the guidelines of this journal. Our experts at SciSpace ensure that. Also, if there's any update in the journal format guidelines, we take care of it and include that in our algorithm.

Sure. We support all the top citation styles like APA style, MLA style, Vancouver style, Harvard style, Chicago style, etc. For example, in case of this journal, when you write your paper and hit autoformat, it will automatically update your article as per the Drug Discovery Today citation style.

You can avail our Free Trial for 7 days. I'm sure you'll find our features very helpful. Plus, it's quite inexpensive.

Yup. You can choose the right template, copy-paste the contents from the word doc and click on auto-format. You'll have a publish-ready paper that you can download at the end.

A matter of seconds. Besides that, our intuitive editor saves a load of your time in writing and formating your manuscript.

One little Google search can get you the Word template for any journal. However, why do you need a Word template when you can write your entire manuscript on SciSpace, autoformat it as per Drug Discovery Today's guidelines and download the same in Word, PDF and LaTeX formats? Try us out!.

Absolutely! You can do it using our intuitive editor. It's very easy. If you need help, you can always contact our support team.

SciSpace is an online tool for now. We'll soon release a desktop version. You can also request (or upvote) any feature that you think might be helpful for you and the research community in the feature request section once you sign-up with us.

Sure. You can request any template and we'll have it up and running within a matter of 3 working days. You can find the request box in the Journal Gallery on the right sidebar under the heading, "Couldn't find the format you were looking for?".

After you have written and autoformatted your paper, you can download it in multiple formats, viz., PDF, Docx and LaTeX.

To be honest, the answer is NO. The impact factor is one of the many elements that determine the quality of a journal. Few of those factors the review board, rejection rates, frequency of inclusion in indexes, Eigenfactor, etc. You must assess all the factors and then take the final call.

SHERPA/RoMEO Database

We have extracted this data from Sherpa Romeo to help our researchers understand the access level of this journal. The following table indicates the level of access a journal has as per Sherpa Romeo Archiving Policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

The 5 most common citation types in order of usage are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

Our journal submission experts are skilled in submitting papers to various international journals.

After uploading your paper on SciSpace, you would see a button to request a journal submission service for Drug Discovery Today.

Each submission service is completed within 4 - 5 working days.

Yes. SciSpace provides this functionality.

After signing up, you would need to import your existing references from Word or .bib file.

SciSpace would allow download of your references in Drug Discovery Today Endnote style, according to elsevier guidelines.

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