Evidence map›Paper›PMID 31913597›Full record

ArticleACS infectious diseases2020

Re-Engineering of Yohimbine's Biological Activity through Ring Distortion: Identification and Structure-Activity Relationships of a New Class of Antiplasmodial Agents.

Nicholas G Paciaroni, David L Perry, Verrill M Norwood, Claribel Murillo-Solano, Jennifer Collins, Srinivasarao Tenneti, Debopam Chakrabarti, Robert W Huigens

Abstract read
In one paragraph

Article in ACS infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
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  5. Review
  6. Review
  7. Antimalarial Natural Products.Progress in the chemistry of organic natural products · 2022
    Article
  8. Article
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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

8 authors.

Nicholas G PaciaroniDepartment of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , 1345 Center Drive , Gainesville , Florida 32610 , United States.ORCID 0000-0001-5799-1544
David L PerryDivision of Molecular Biology and Microbiology, Burnett School of Biomedical Sciences , University of Central Florida , 12722 Research Parkway , Orlando , Florida 32826 , United States.
Verrill M NorwoodDepartment of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , 1345 Center Drive , Gainesville , Florida 32610 , United States.
Claribel Murillo-SolanoDivision of Molecular Biology and Microbiology, Burnett School of Biomedical Sciences , University of Central Florida , 12722 Research Parkway , Orlando , Florida 32826 , United States.ORCID 0000-0002-8116-7181
Jennifer CollinsDivision of Molecular Biology and Microbiology, Burnett School of Biomedical Sciences , University of Central Florida , 12722 Research Parkway , Orlando , Florida 32826 , United States.ORCID 0000-0002-1195-4630
Srinivasarao TennetiDepartment of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , 1345 Center Drive , Gainesville , Florida 32610 , United States.ORCID 0000-0002-6687-8348
Debopam ChakrabartiDivision of Molecular Biology and Microbiology, Burnett School of Biomedical Sciences , University of Central Florida , 12722 Research Parkway , Orlando , Florida 32826 , United States.ORCID 0000-0002-4554-3119
Robert W HuigensDepartment of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , 1345 Center Drive , Gainesville , Florida 32610 , United States.ORCID 0000-0003-3811-2721

Funding

Indole Alkaloids and Phenazine Antibiotics: New Platforms for Drug DiscoveryR35GM128621 · NIGMS · UNIVERSITY OF FLORIDA · PI HUIGENS, ROBERT WILLIAM · 2018 to 2022
$1.7M
NIGMS NIH HHS R35 GM128621
6 · The paper itself

Abstract

Select natural products are ideal starting points for ring distortion, or the dramatic altering of inherently complex molecules through short synthetic pathways, to generate an array of novel compounds with diverse skeletal architectures. A major goal of our ring distortion approach is to re-engineer the biological activity of indole alkaloids to identify new compounds with diverse biological activities in areas of significance to human health and medicine. In this study, we re-engineered the biological activity of the indole alkaloid yohimbine through ring rearrangement and ring cleavage synthesis pathways to discover new series of antiplasmodial agents. One new compound,

Indexed as

Drug DiscoveryAntimalarialsBiological ProductsChloroquineDrug ResistanceHep G2 CellsHumansIndole AlkaloidsMalariaMolecular StructureParasitic Sensitivity TestsPlasmodium falciparumStructure-Activity RelationshipTrophozoitesYohimbineAntimalarialsBiological ProductsChloroquineIndole AlkaloidsYohimbinedrug discoveryindole alkaloidsmalariaring distortionyohimbine

Identifiers

PMID31913597
PMCPMC7346850

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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.