Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines

In this data file the synthetic procedures for preparation of the original 4-pyridinium-1,4-dihydropyridines (4-Py-1,4-DHP) and their parent compounds – dialkyl 2,6-dimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylates were described. In total, 5 unpublished compounds were obtained and chara...

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Main Authors: Klavs Pajuste, Martins Rucins, Ilona Domracheva, Arkadij Sobolev, Nadiia Pikun, Mara Plotniece, Gunars Duburs, Karlis Pajuste, Aiva Plotniece
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:Data in Brief
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S235234092031427X
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spelling doaj-9223f1ff398c4a9fa9d5e86a17f8d9da2020-12-21T04:44:57ZengElsevierData in Brief2352-34092020-12-0133106545Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridinesKlavs Pajuste0Martins Rucins1Ilona Domracheva2Arkadij Sobolev3Nadiia Pikun4Mara Plotniece5Gunars Duburs6Karlis Pajuste7Aiva Plotniece8Latvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, Latvia; Corresponding author.Latvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Riga Stradiņš University, Dzirciema str. 16, LV-1007, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006, Riga, LatviaIn this data file the synthetic procedures for preparation of the original 4-pyridinium-1,4-dihydropyridines (4-Py-1,4-DHP) and their parent compounds – dialkyl 2,6-dimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylates were described. In total, 5 unpublished compounds were obtained and characterised. All the structures of original compounds were confirmed by Nuclear Magnetic Resonance (NMR, including 1H NMR and 13C NMR) and low resolution mass spectra (MS) data. Additionally, the cytotoxic properties of four 4-Py-1,4-DHPs were evaluated on 3 cell lines – normal NIH3T3 (mouse embryonic fibroblast), cancerous HT-1080 (human lung fibrosarcoma) and MH-22A (mouse hepatoma) and self-assembling properties were studied and characterisation of formed nanoparticles were performed using dynamic light scattering technique. In this article provided data are directly related to the previously published research articles – “Novel cationic amphiphilic 1,4-dihydropyridine derivatives for DNA delivery” [1] where compound 5 was tested as gene delivery agent without full physico-chemical characterisation and “Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1,4-dihydropyridine derivatives” [2] where synthesis and physico-chemical characterisation as well as calcium channel blocking and antioxidant activities were described for compound 6. Synthesis of other compounds – parent 1,4-DHPs 1 and 2, and 4-Py-1,4-DHPs 3–5, their characterisation, estimation of cytotoxicity and self-assembling properties for all 4-Py-1,4-DHPs 3–6 are reported herein for the first time. Information provided in this data file can be used in medicinal chemistry by other scientists to estimate structure-activity relationships for the analysis and construction of various cationic 1,4-dihydropyridine derivatives and related heterocycles.http://www.sciencedirect.com/science/article/pii/S235234092031427X1,4-dihydropyridinePyridiniumQuaternisationCytotoxicitySelf-assemblingNanoparticles
collection DOAJ
language English
format Article
sources DOAJ
author Klavs Pajuste
Martins Rucins
Ilona Domracheva
Arkadij Sobolev
Nadiia Pikun
Mara Plotniece
Gunars Duburs
Karlis Pajuste
Aiva Plotniece
spellingShingle Klavs Pajuste
Martins Rucins
Ilona Domracheva
Arkadij Sobolev
Nadiia Pikun
Mara Plotniece
Gunars Duburs
Karlis Pajuste
Aiva Plotniece
Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
Data in Brief
1,4-dihydropyridine
Pyridinium
Quaternisation
Cytotoxicity
Self-assembling
Nanoparticles
author_facet Klavs Pajuste
Martins Rucins
Ilona Domracheva
Arkadij Sobolev
Nadiia Pikun
Mara Plotniece
Gunars Duburs
Karlis Pajuste
Aiva Plotniece
author_sort Klavs Pajuste
title Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
title_short Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
title_full Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
title_fullStr Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
title_full_unstemmed Data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
title_sort data for the cytotoxicity, self-assembling properties and synthesis of 4-pyridinium-1,4-dihydropyridines
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2020-12-01
description In this data file the synthetic procedures for preparation of the original 4-pyridinium-1,4-dihydropyridines (4-Py-1,4-DHP) and their parent compounds – dialkyl 2,6-dimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylates were described. In total, 5 unpublished compounds were obtained and characterised. All the structures of original compounds were confirmed by Nuclear Magnetic Resonance (NMR, including 1H NMR and 13C NMR) and low resolution mass spectra (MS) data. Additionally, the cytotoxic properties of four 4-Py-1,4-DHPs were evaluated on 3 cell lines – normal NIH3T3 (mouse embryonic fibroblast), cancerous HT-1080 (human lung fibrosarcoma) and MH-22A (mouse hepatoma) and self-assembling properties were studied and characterisation of formed nanoparticles were performed using dynamic light scattering technique. In this article provided data are directly related to the previously published research articles – “Novel cationic amphiphilic 1,4-dihydropyridine derivatives for DNA delivery” [1] where compound 5 was tested as gene delivery agent without full physico-chemical characterisation and “Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1,4-dihydropyridine derivatives” [2] where synthesis and physico-chemical characterisation as well as calcium channel blocking and antioxidant activities were described for compound 6. Synthesis of other compounds – parent 1,4-DHPs 1 and 2, and 4-Py-1,4-DHPs 3–5, their characterisation, estimation of cytotoxicity and self-assembling properties for all 4-Py-1,4-DHPs 3–6 are reported herein for the first time. Information provided in this data file can be used in medicinal chemistry by other scientists to estimate structure-activity relationships for the analysis and construction of various cationic 1,4-dihydropyridine derivatives and related heterocycles.
topic 1,4-dihydropyridine
Pyridinium
Quaternisation
Cytotoxicity
Self-assembling
Nanoparticles
url http://www.sciencedirect.com/science/article/pii/S235234092031427X
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