Example of Molecular Diversity format
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Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format Example of Molecular Diversity format
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open access Open Access

Molecular Diversity — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Information Systems #129 of 329 down down by 43 ranks
Inorganic Chemistry #30 of 69 up up by 3 ranks
Physical and Theoretical Chemistry #77 of 169 down down by 3 ranks
Organic Chemistry #88 of 185 down down by 3 ranks
Drug Discovery #83 of 145 down down by 4 ranks
Catalysis #36 of 57 down down by 3 ranks
Molecular Biology #271 of 382 down down by 13 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 323 Published Papers | 1131 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 24/06/2020
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Related Journals

open access Open Access
recommended Recommended

Wiley

Quality:  
High
CiteRatio: 8.3
SJR: 1.497
SNIP: 0.954
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American Chemical Society

Quality:  
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SJR: 1.231
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Elsevier

Quality:  
High
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open access Open Access

Elsevier

Quality:  
Good
CiteRatio: 5.4
SJR: 0.803
SNIP: 1.408

Journal Performance & Insights

Impact Factor

CiteRatio

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.

A measure of average citations received per peer-reviewed paper published in the journal.

2.013

1% from 2018

Impact factor for Molecular Diversity from 2016 - 2019
Year Value
2019 2.013
2018 2.032
2017 2.229
2016 1.752
graph view Graph view
table view Table view

3.5

8% from 2019

CiteRatio for Molecular Diversity from 2016 - 2020
Year Value
2020 3.5
2019 3.8
2018 3.7
2017 3.4
2016 3.5
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 1% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 8% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.385

5% from 2019

SJR for Molecular Diversity from 2016 - 2020
Year Value
2020 0.385
2019 0.368
2018 0.482
2017 0.494
2016 0.463
graph view Graph view
table view Table view

0.741

1% from 2019

SNIP for Molecular Diversity from 2016 - 2020
Year Value
2020 0.741
2019 0.735
2018 0.697
2017 0.724
2016 0.57
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 5% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 1% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Molecular Diversity

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Springer

Molecular Diversity

Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishe...... Read More

Medicine

i
Last updated on
23 Jun 2020
i
ISSN
1381-1991
i
Impact Factor
Medium - 0.95
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
i
Citation Type
Author Year
(Blonder et al, 1982)
i
Bibliography Example
Beenakker CWJ (2006) Specular andreev reflection in graphene. Phys Rev Lett 97(6):067,007, URL 10.1103/PhysRevLett.97.067007

Top papers written in this journal

Journal Article DOI: 10.1007/S11030-009-9138-8
Controlled microwave heating in modern organic synthesis: highlights from the 2004–2008 literature
C. Oliver Kappe1, Doris Dallinger1
21 Apr 2009 - Molecular Diversity

Abstract:

Direct and rapid heating by microwave irradiation in combination with sealed vessel processing in many cases enables reactions to be carried out in a fraction of the time generally required using conventional conditions. This makes microwave chemistry an ideal tool for rapid reaction scouting and optimization of conditions, a... Direct and rapid heating by microwave irradiation in combination with sealed vessel processing in many cases enables reactions to be carried out in a fraction of the time generally required using conventional conditions. This makes microwave chemistry an ideal tool for rapid reaction scouting and optimization of conditions, allowing very rapid progress through hypotheses–experiment–results iterations. The speed at which multiple variations of reaction conditions can be performed allows a morning discussion of “What should we try?” to become an after-lunch discussion of “What were the results” Not surprisingly, therefore, many scientists both in academia and industry have turned to microwave synthesis as a front-line methodology for their projects. In this review, more than 220 published examples of microwave-assisted synthetic organic transformations from the 2004 to 2008 literature are discussed. An additional ca. 500 reaction schemes are presented in the Electronic Supplementary Material, providing the reader with an overall number of ca. 930 references in this fast-moving and exciting field. read more read less
423 Citations
Journal Article DOI: 10.1023/A:1021372108686
Predictive QSAR modeling based on diversity sampling of experimental datasets for the training and test set selection.
Alexander Golbraikh1, Alexander Tropsha1
01 Dec 2000 - Molecular Diversity

Abstract:

One of the most important characteristics of Quantitative Structure Activity Relashionships (QSAR) models is their predictive power. The latter can be defined as the ability of a model to predict accurately the target property (e.g., biological activity) of compounds that were not used for model development. We suggest that t... One of the most important characteristics of Quantitative Structure Activity Relashionships (QSAR) models is their predictive power. The latter can be defined as the ability of a model to predict accurately the target property (e.g., biological activity) of compounds that were not used for model development. We suggest that this goal can be achieved by rational division of an experimental SAR dataset into the training and test set, which are used for model development and validation, respectively. Given that all compounds are represented by points in multidimensional descriptor space, we argue that training and test sets must satisfy the following criteria: (i) Representative points of the test set must be close to those of the training set; (ii) Representative points of the training set must be close to representative points of the test set; (iii) Training set must be diverse. For quantitative description of these criteria, we use molecular dataset diversity indices introduced recently (Golbraikh, A., J. Chem. Inf. Comput. Sci., 40 (2000) 414-425). For rational division of a dataset into the training and test sets, we use three closely related sphere-exclusion algorithms. Using several experimental datasets, we demonstrate that QSAR models built and validated with our approach have statistically better predictive power than models generated with either random or activity ranking based selection of the training and test sets. We suggest that rational approaches to the selection of training and test sets based on diversity principles should be used routinely in all QSAR modeling research. read more read less

Topics:

Test set (63%)63% related to the paper
301 Citations
Journal Article DOI: 10.1007/S11030-015-9629-8
Molecular diversity of spirooxindoles. Synthesis and biological activity
01 Feb 2016 - Molecular Diversity

Abstract:

Spirooxindoles are important synthetic targets possessing extended biological activity and drug discovery applications. This review focuses on the various strategies for the enantioselective synthesis of spirocyclic oxindoles relying on reports over the past decade and from earlier work. The spirooxindoles in this review are ... Spirooxindoles are important synthetic targets possessing extended biological activity and drug discovery applications. This review focuses on the various strategies for the enantioselective synthesis of spirocyclic oxindoles relying on reports over the past decade and from earlier work. The spirooxindoles in this review are separated into three structural classes, and then further categorized into the method type from which the spirocycle is generated. read more read less
254 Citations
Journal Article DOI: 10.1007/S11030-006-9027-3
Molecular and functional diversity of vascular endothelial growth factors.
Yasuo Yamazaki1, Takashi Morita1
14 Sep 2006 - Molecular Diversity

Abstract:

Members of the vascular endothelial growth factor (VEGF) family are crucial regulators of neovascularization and are classified as cystine knot growth factors that specifically bind cellular receptor tyrosine kinases VEGFR-1, VEGFR-2, and VEGFR-3 with high but variable affinity and selectivity. The VEGF family has recently be... Members of the vascular endothelial growth factor (VEGF) family are crucial regulators of neovascularization and are classified as cystine knot growth factors that specifically bind cellular receptor tyrosine kinases VEGFR-1, VEGFR-2, and VEGFR-3 with high but variable affinity and selectivity. The VEGF family has recently been expanded and currently comprises seven members: VEGF-A, VEGF-B, placenta growth factor (PlGF), VEGF-C, VEGF-D, viral VEGF (also known as VEGF-E), and snake venom VEGF (also known as VEGF-F). Although all members are structurally homologous, there is molecular diversity among the subtypes, and several isoforms, such as VEGF-A, VEGF-B, and PlGF, are generated by alternative exon splicing. These splicing isoforms exhibit differing properties, particularly in binding to co-receptor neuropilins and heparin. VEGF family proteins play multiple physiological roles, such as angiogenesis and lymphangiogenesis, while exogenous members (viral and snake venom VEGFs) display activities that are unique in physiology and function. This review will highlight the molecular and functional diversity of VEGF family proteins. read more read less

Topics:

Vascular endothelial growth factor (59%)59% related to the paper, Neuropilins (57%)57% related to the paper, Vascular endothelial growth factor B (56%)56% related to the paper, Kinase insert domain receptor (56%)56% related to the paper, Vascular endothelial growth factor C (54%)54% related to the paper
232 Citations
Journal Article DOI: 10.1007/S11030-006-8697-1
Molecular similarity and diversity in chemoinformatics: from theory to applications.
Ana G. Maldonado1, Jean-Pierre Doucet1, Michel Petitjean1, Botao Fan1
01 Feb 2006 - Molecular Diversity

Abstract:

This review is dedicated to a survey on molecular similarity and diversity. Key findings reported in recent investigations are selectively highlighted and summarized. Even if this overview is mainly centered in chemoinformatics, applications in other areas (pharmaceutical and medical chemistry, combinatorial chemistry, chemic... This review is dedicated to a survey on molecular similarity and diversity. Key findings reported in recent investigations are selectively highlighted and summarized. Even if this overview is mainly centered in chemoinformatics, applications in other areas (pharmaceutical and medical chemistry, combinatorial chemistry, chemical databases management, etc.) are also introduced. The approaches used to define and descript the concepts of molecular similarity and diversity in the context of chemoinformatics are discussed in the first part of this review. We introduce, in the second and third parts, the descriptions and analyses of different methods and techniques. Finally, current applications and problems are enumerated and discussed in the last part. read more read less

Topics:

Cheminformatics (51%)51% related to the paper
221 Citations
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Molecular Diversity format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Molecular Diversity in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Molecular Diversity guidelines and auto format it.

2. Do you follow the Molecular Diversity guidelines?

Yes, the template is compliant with the Molecular Diversity guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Molecular Diversity?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Molecular Diversity citation style.

4. Can I use the Molecular Diversity templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Molecular Diversity.

5. Can I use a manuscript in Molecular Diversity that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Molecular Diversity that you can download at the end.

6. How long does it usually take you to format my papers in Molecular Diversity?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Molecular Diversity.

7. Where can I find the template for the Molecular Diversity?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Molecular Diversity's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Molecular Diversity's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Molecular Diversity an online tool or is there a desktop version?

SciSpace's Molecular Diversity is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Molecular Diversity?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Molecular Diversity?”

11. What is the output that I would get after using Molecular Diversity?

After writing your paper autoformatting in Molecular Diversity, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Molecular Diversity's impact factor high enough that I should try publishing my article there?

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 these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Molecular Diversity?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Molecular Diversity. The table below indicates the level of access a journal has as per Sherpa Romeo's 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.

14. What are the most common citation types In Molecular Diversity?

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

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

15. How do I submit my article to the Molecular Diversity?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Molecular Diversity's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Molecular Diversity in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Molecular Diversity Endnote style according to Elsevier guidelines.

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