Evidence map›Paper›PMID 25161722›Full record

ArticleBeilstein journal of organic chemistry2014

Synthesis of isoprenoid bisphosphonate ethers through C-P bond formations: Potential inhibitors of geranylgeranyl diphosphate synthase.

Xiang Zhou, Jacqueline E Reilly, Kathleen A Loerch, Raymond J Hohl, David F Wiemer

Open access · diamondAbstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Phosphonic acid: preparation and applications.Beilstein journal of organic chemistry · 2017
    Review
  10. Article
  11. Article
  12. Article
  13. Article
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

5 authors at 1 institution in 1 country.

Xiang ZhouDepartment of Chemistry, University of Iowa, Iowa City, Iowa 52242-1294, USA.
Jacqueline E ReillyDepartment of Pharmacology, University of Iowa, Iowa City, Iowa 52242-1294, USA.
Kathleen A LoerchDepartment of Chemistry, University of Iowa, Iowa City, Iowa 52242-1294, USA.
Raymond J HohlDepartment of Pharmacology, University of Iowa, Iowa City, Iowa 52242-1294, USA ; Department of Internal Medicine, University of Iowa, Iowa City, Iowa 52242-1294, USA.
David F WiemerDepartment of Chemistry, University of Iowa, Iowa City, Iowa 52242-1294, USA ; Department of Pharmacology, University of Iowa, Iowa City, Iowa 52242-1294, USA.
University of Iowa · US

Funding

Predoctoral Training in the Pharmacological SciencesT32GM067795 · NIGMS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2004 to 2021
$3.4M
NIGMS NIH HHS T32 GM067795
6 · The paper itself

Abstract

A set of bisphosphonate ethers has been prepared through sequential phosphonylation and alkylation of monophosphonate ethers. After formation of the corresponding phosphonic acid salts, these compounds were tested for their ability to inhibit the enzyme geranylgeranyl diphosphate synthase (GGDPS). Five of the new compounds show IC50 values of less than 1 μM against GGDPS with little to no activity against the related enzyme farnesyl diphosphate synthase (FDPS). The most active compound displayed an IC50 value of 82 nM when assayed with GGDPS, and no activity against FDPS even at a 10 μM concentration.

Indexed as

bisphosphonateisoprenoid biosynthesisorganophosphorousphosphonate formation

Identifiers

PMID25161722
PMCPMC4142842
OpenAlexW2134567993

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.