Evidence map›Paper›PMID 24102367›Full record

ArticleOrganic letters2013

Conformational preferences of zampanolide and dactylolide.

Erik M Larsen, Matthew R Wilson, Jaroslav Zajicek, Richard E Taylor

Abstract read
In one paragraph

Article in Organic letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Hydrocarbon Macrocycle Conformer Ensembles andAngewandte Chemie (International ed. in English) · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Erik M LarsenDepartment of Chemistry & Biochemistry and the Harper Cancer Research Institute, University of Notre Dame , 251 Nieuwland Science Hall, Notre Dame, Indiana 46556-5670, United States.
Matthew R Wilson
Jaroslav Zajicek
Richard E Taylor

Funding

Synthesis and Biosynthesis of Pyran and Spiroketal Structural UnitsR01GM084922 · NIGMS · UNIVERSITY OF NOTRE DAME · PI TAYLOR, RICHARD E. · 2010 to 2013
$1.1M
CONFORMATION ACTIVITY RELATIONSHIPSR01CA085499 · NCI · UNIVERSITY OF NOTRE DAME · PI TAYLOR, RICHARD E · 2000 to 2003
$669k
NCI NIH HHS R01 CA085499NIGMS NIH HHS GM084922NIGMS NIH HHS R01 GM084922
6 · The paper itself

Abstract

The solution conformation behavior of the macrolide core of microtubule-stabilizing agents (-)-zampanolide and (-)-dactylolide has been determined through a combination of high-field NMR experiments and computational modeling. Taken together, the results demonstrate that in solution both molecules exist as a mixture of three interconverting conformational families, one of which bears strong resemblance to zampanolide's tubulin-bound conformation.

Indexed as

Bridged Bicyclo Compounds, HeterocyclicLactonesMacrolidesMagnetic Resonance SpectroscopyModels, MolecularMolecular ConformationMonte Carlo MethodStereoisomerismBridged Bicyclo Compounds, HeterocyclicdactylolideLactonesMacrolideszampanolide

Identifiers

PMID24102367
PMCPMC3946545

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.