Evidence map›Paper›PMID 17914846›Full record

ArticleThe Journal of organic chemistry2007

Synthesis and spectral properties of cholesterol- and FTY720-containing boron dipyrromethene dyes.

Zaiguo Li, Robert Bittman

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Synthesis and Biological Evaluation of BODIPY-PF-543.Molecules (Basel, Switzerland) · 2019
    Article
  5. Article
  6. Article
  7. α-Synuclein Regulates Neuronal Cholesterol Efflux.Molecules (Basel, Switzerland) · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Peptide conjugation via CuAAC 'click' chemistry.Molecules (Basel, Switzerland) · 2013
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Sphingosine 1-phosphate lyase enzyme assay using a BODIPY-labeled substrate.Biochemical and biophysical research communications · 2009
    Article
  19. Review
  20. 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

2 authors.

Zaiguo LiDepartment of Chemistry and Biochemistry, Queens College of City University of New York, Flushing, New York 11367-1597, USA.
Robert Bittman

Funding

Synthesis of Novel Bioactive Sphingolipids as a ResourceR24HL083187 · NHLBI · QUEENS COLLEGE · PI BITTMAN, ROBERT · 2006 to 2013
$2.5M
NHLBI NIH HHS HL-083187NHLBI NIH HHS R24 HL083187
6 · The paper itself

Abstract

Two analogues (1, 2) of free cholesterol and one analogue (3) of the immunosuppressive sphingolipid FTY720 containing a boron dipyrromethene chromophore (BODIPY) were synthesized. The synthetic routes involved preparation of boron dipyrromethene moieties (5, 11), bearing a phenylethynyl group at different positions of the chromophore, and lipids (13, 20) bearing an azido group. The dye was tethered to the lipid via a 1,2,3-triazole in the linker by the click reaction. Analogues derived from 11 [in which an (E)-styrylethynyl moiety is bonded to C-5 of BODIPY] exhibited a marked red shift (approximately 70-80 nm) compared with those derived from 5 (in which a phenylethynyl moiety is bonded to C-8 of BODIPY).

Indexed as

Boron CompoundsCholesterolFingolimod HydrochlorideFluorescent DyesMolecular StructurePorphobilinogenPropylene GlycolsSpectrophotometry, UltravioletSphingosineStereoisomerismBoron CompoundsCholesteroldipyrrometheneFingolimod HydrochlorideFluorescent DyesPorphobilinogenPropylene GlycolsSphingosine

Identifiers

PMID17914846
PMCPMC2547128

What OpenQuestion holds

Textmetadata
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.