Evidence map›Paper›PMID 22082008›Full record

ArticleJournal of medicinal chemistry2011

Retooling manganese(III) porphyrin-based peroxynitrite decomposition catalysts for selectivity and oral activity: a potential new strategy for treating chronic pain.

Smita Rausaria, Mahsa M E Ghaffari, Andrew Kamadulski, Kenny Rodgers, Leesa Bryant, Zhoumou Chen, Tim Doyle, Michael J Shaw, Daniela Salvemini, William L Neumann

Open access · greenAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  13. Reciprocal regulation of the nitric oxide and cyclooxygenase pathway in pathophysiology: relevance and clinical implications.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Review
  14. Design, mechanism of action, bioavailability and therapeutic effects of mn porphyrin-based redox modulators.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2013
    Review
  15. Targeting the overproduction of peroxynitrite for the prevention and reversal of paclitaxel-induced neuropathic pain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  16. 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

10 authors at 1 institution in 1 country.

Smita RausariaDepartment of Pharmaceutical Sciences, School of Pharmacy, Southern Illinois University, Edwardsville, Illinois 62026, United States.
Mahsa M E Ghaffari
Andrew Kamadulski
Kenny Rodgers
Leesa Bryant
Zhoumou Chen
Tim Doyle
Michael J Shaw
Daniela Salvemini
William L Neumann
Saint Louis University · US

Funding

Targeting the relief of chronic pain with orally active peroxynitrite decompositiRC1AR058231 · NIAMS · SOUTHERN ILLINOIS UNIV AT EDWARDSVILLE · PI NEUMANN, WILLIAM, SALVEMINI, DANIELA · 2009 to 2010
$974k
NIAMS NIH HHS RC1 AR058231NIAMS NIH HHS RC1AR058231
6 · The paper itself

Abstract

Redox-active metalloporphyrins represent the most well-characterized class of catalysts capable of attenuating oxidative stress in vivo through the direct interception and decomposition of superoxide and peroxynitrite. While many interesting pharmacological probes have emerged from these studies, few catalysts have been developed with pharmaceutical properties in mind. Herein, we describe our efforts to identify new Mn(III)-porphyrin systems with enhanced membrane solubilizing properties. To this end, seven new Mn(III)-tetracyclohexenylporphyin (TCHP) analogues, 7, 10, 12, 15, and 16a-c, have been prepared in which the beta-fused cyclohexenyl rings provide a means to shield the charged metal center from the membrane during passive transport. Compounds 7, 15, and 16a-c have been shown to be orally active and potent analgesics in a model of carrageenan-induced thermal hyperalgesia. In addition, oral administration of compound 7 (10-100 mg/kg, n=5) has been shown to dose dependently reverse mechano-allodynia in the CCI model of chronic neuropathic pain.

Indexed as

ManganeseAdministration, OralAnalgesicsAnimalsBoronic AcidsCarrageenanCatalysisChronic PainElectrochemistryHyperalgesiaMetalloporphyrinsMiceNeuralgiaPeroxynitrous AcidRatsSciatic NerveAnalgesicsBoronic AcidsCarrageenanManganeseMetalloporphyrinsPeroxynitrous AcidSuperoxide Dismutase

Identifiers

PMID22082008
PMCPMC3240686
OpenAlexW1963571701

What OpenQuestion holds

Textmetadata
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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.