Evidence map›Paper›PMID 31057026›Full record

ReviewPharmaceutical biology2019

HPLC-based activity profiling for pharmacologically and toxicologically relevant natural products - principles and recent examples.

Matthias Hamburger

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. International journal of molecular sciences · 2024
    Article
  6. Review
  7. Article
  8. Metabolites ofMetabolites · 2023
    Article
  9. Article
  10. Review
  11. 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

1 author at 1 institution in 1 country.

Matthias Hamburgera Pharmaceutical Biology, Pharmacenter , University of Basel , Basel , Switzerland.
University of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextDiscovery of pharmacologically active natural products as starting points for drug development remains important and, for reasons of consumer safety, the identification of toxicologically relevant compounds in herbal drugs.

objectiveTo explain, with the aid of relevant examples from our own research, how these goals can be achieved.

methodsAn in-house technology platform comprising pre-formatted extract libraries in 96-well format, miniaturized tracking of activity in extracts via HPLC-activity profiling, structure elucidation with microprobe NMR, and in vitro and in vivo pharmacological methods were used.

resultsPiperine was identified as a new scaffold for allosteric GABA

conclusionsThe allosteric binding site for piperine analogues remains to be characterized and cardiac risks of herbal drugs need to be further evaluated to ensure consumer safety.

Indexed as

AnimalsBinding SitesChromatography, High Pressure LiquidDrug DiscoveryERG1 Potassium ChannelGABA ModulatorsHumansMolecular StructurePlant PreparationsPotassium Channel BlockersReceptors, GABA-AStructure-Activity RelationshipERG1 Potassium ChannelGABA ModulatorsKCNH2 protein, humanPlant PreparationsPotassium Channel BlockersReceptors, GABA-AdehydroevodiamineGABAA receptorhERGhortiaminepiperine

Identifiers

PMID31057026
PMCPMC6507960
OpenAlexW2944425800

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.