Synthesis of Nitrostyrylthiazolidine-2,4-dione Derivatives Displaying Antileishmanial Potential.

Saved in:
Bibliographic Details
Title: Synthesis of Nitrostyrylthiazolidine-2,4-dione Derivatives Displaying Antileishmanial Potential.
Authors: Khoumeri O; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France., Hutter S; IHU Méditerranée Infection, UMR RITMES, TEAM-VEPTE, Aix Marseille University, 19-21 Boulevard Jean Moulin, 13005 Marseille, France., Primas N; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France., Castera-Ducros C; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France., Carvalho S; Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK., Wyllie S; Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK., Efrit ML; Laboratoire de Synthèse Organique et Hétérocyclique Sélective-Evaluation D'activité Biologique, LR17ES01, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, Tunis 2092, Tunisia., Fayolle D; Normandie Université, UNICAEN, CERMN, DruiD Platform, Boulevard Becquerel, 14000 Caen, France., Since M; Normandie Université, UNICAEN, CERMN, DruiD Platform, Boulevard Becquerel, 14000 Caen, France., Vanelle P; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France., Verhaeghe P; CNRS, Département de Pharmacochimie Moléculaire UMR 5063, University Grenoble Alpes, 38041 Grenoble, France.; LCC-CNRS, UPR8241, Laboratoire de Chimie de Coordination, Université de Toulouse, CNRS, UPS, 31400 Toulouse, France., Azas N; IHU Méditerranée Infection, UMR RITMES, TEAM-VEPTE, Aix Marseille University, 19-21 Boulevard Jean Moulin, 13005 Marseille, France., El-Kashef H; Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.; Faculty of Pharmacy, Sphinx University, Regional Road, New Assiut 71515, Egypt.
Source: Pharmaceuticals (Basel, Switzerland) [Pharmaceuticals (Basel)] 2024 Jul 03; Vol. 17 (7). Date of Electronic Publication: 2024 Jul 03.
Publication Type: Journal Article
Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101238453 Publication Model: Electronic Cited Medium: Print ISSN: 1424-8247 (Print) Linking ISSN: 14248247 NLM ISO Abbreviation: Pharmaceuticals (Basel) Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 39065730
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Synthesis of Nitrostyrylthiazolidine-2,4-dione Derivatives Displaying Antileishmanial Potential.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Khoumeri+O%22">Khoumeri O</searchLink>; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.<br /><searchLink fieldCode="AU" term="%22Hutter+S%22">Hutter S</searchLink>; IHU Méditerranée Infection, UMR RITMES, TEAM-VEPTE, Aix Marseille University, 19-21 Boulevard Jean Moulin, 13005 Marseille, France.<br /><searchLink fieldCode="AU" term="%22Primas+N%22">Primas N</searchLink>; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France.<br /><searchLink fieldCode="AU" term="%22Castera-Ducros+C%22">Castera-Ducros C</searchLink>; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France.<br /><searchLink fieldCode="AU" term="%22Carvalho+S%22">Carvalho S</searchLink>; Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.<br /><searchLink fieldCode="AU" term="%22Wyllie+S%22">Wyllie S</searchLink>; Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.<br /><searchLink fieldCode="AU" term="%22Efrit+ML%22">Efrit ML</searchLink>; Laboratoire de Synthèse Organique et Hétérocyclique Sélective-Evaluation D'activité Biologique, LR17ES01, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, Tunis 2092, Tunisia.<br /><searchLink fieldCode="AU" term="%22Fayolle+D%22">Fayolle D</searchLink>; Normandie Université, UNICAEN, CERMN, DruiD Platform, Boulevard Becquerel, 14000 Caen, France.<br /><searchLink fieldCode="AU" term="%22Since+M%22">Since M</searchLink>; Normandie Université, UNICAEN, CERMN, DruiD Platform, Boulevard Becquerel, 14000 Caen, France.<br /><searchLink fieldCode="AU" term="%22Vanelle+P%22">Vanelle P</searchLink>; Team Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Aix Marseille University, CNRS, ICR UMR 7273, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France.; Service Central de la Qualité et de l'Information Pharmaceutiques, Hôpital de la Conception, AP-HM, 147 Boulevard Baille, 13005 Marseille, France.<br /><searchLink fieldCode="AU" term="%22Verhaeghe+P%22">Verhaeghe P</searchLink>; CNRS, Département de Pharmacochimie Moléculaire UMR 5063, University Grenoble Alpes, 38041 Grenoble, France.; LCC-CNRS, UPR8241, Laboratoire de Chimie de Coordination, Université de Toulouse, CNRS, UPS, 31400 Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Azas+N%22">Azas N</searchLink>; IHU Méditerranée Infection, UMR RITMES, TEAM-VEPTE, Aix Marseille University, 19-21 Boulevard Jean Moulin, 13005 Marseille, France.<br /><searchLink fieldCode="AU" term="%22El-Kashef+H%22">El-Kashef H</searchLink>; Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.; Faculty of Pharmacy, Sphinx University, Regional Road, New Assiut 71515, Egypt.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101238453%22">Pharmaceuticals (Basel, Switzerland)</searchLink> [Pharmaceuticals (Basel)] 2024 Jul 03; Vol. 17 (7). <i>Date of Electronic Publication: </i>2024 Jul 03.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22MDPI%22">MDPI </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101238453 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>1424-8247 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214248247%22">14248247 </searchLink><i>NLM ISO Abbreviation: </i>Pharmaceuticals (Basel) <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39065730
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3390/ph17070878
    Languages:
      – Code: eng
        Text: English
    Titles:
      – TitleFull: Synthesis of Nitrostyrylthiazolidine-2,4-dione Derivatives Displaying Antileishmanial Potential.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Khoumeri O
      – PersonEntity:
          Name:
            NameFull: Hutter S
      – PersonEntity:
          Name:
            NameFull: Primas N
      – PersonEntity:
          Name:
            NameFull: Castera-Ducros C
      – PersonEntity:
          Name:
            NameFull: Carvalho S
      – PersonEntity:
          Name:
            NameFull: Wyllie S
      – PersonEntity:
          Name:
            NameFull: Efrit ML
      – PersonEntity:
          Name:
            NameFull: Fayolle D
      – PersonEntity:
          Name:
            NameFull: Since M
      – PersonEntity:
          Name:
            NameFull: Vanelle P
      – PersonEntity:
          Name:
            NameFull: Verhaeghe P
      – PersonEntity:
          Name:
            NameFull: Azas N
      – PersonEntity:
          Name:
            NameFull: El-Kashef H
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 03
              M: 07
              Text: 2024 Jul 03
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 1424-8247
          Numbering:
            – Type: volume
              Value: 17
            – Type: issue
              Value: 7
          Titles:
            – TitleFull: Pharmaceuticals (Basel, Switzerland)
              Type: main
ResultId 1