Synthesis of 1,4-dihydropyridine derivatives having an oxy-, alkoxy-, or dimethylaminophenyl substituent in the 4 position, their antioxidant activity, and their ... View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1996-10

AUTHORS

M. Plotnietse, G. Tirzitis, Ya. Uldrikis, Zh. Koronova, D. Tirzite, N. Makarova, G. Dahurs

ABSTRACT

The method of Hantzsch was used to synthesize esters and amides of 2,6-dimethyl-4-aryl-1,4-dihydropyridine-3,5-dicarboxylic acid, containing electron donor substituents in the phenyl ring. It was found that in addition to their antioxidant properties, 3,5-diamides and 4-(3′,4′-dioxyphenyl) derivatives have an affinity for model phospholipid membranes.

PAGES

1166-1172

References to SciGraph publications

  • 1968-09. A rapid method for evaluation of antioxidants in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • 1971-02. A simplified method for the evaluation of antioxidants in JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/bf01169228

    DOI

    http://dx.doi.org/10.1007/bf01169228

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1002640617


    Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
    Incoming Citations Browse incoming citations for this publication using opencitations.net

    JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

    [
      {
        "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "about": [
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0306", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Physical Chemistry (incl. Structural)", 
            "type": "DefinedTerm"
          }, 
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Chemical Sciences", 
            "type": "DefinedTerm"
          }
        ], 
        "author": [
          {
            "familyName": "Plotnietse", 
            "givenName": "M.", 
            "id": "sg:person.012155141657.93", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012155141657.93"
            ], 
            "type": "Person"
          }, 
          {
            "familyName": "Tirzitis", 
            "givenName": "G.", 
            "id": "sg:person.01360231013.54", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01360231013.54"
            ], 
            "type": "Person"
          }, 
          {
            "familyName": "Uldrikis", 
            "givenName": "Ya.", 
            "id": "sg:person.012211761547.48", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012211761547.48"
            ], 
            "type": "Person"
          }, 
          {
            "familyName": "Koronova", 
            "givenName": "Zh.", 
            "id": "sg:person.07606461663.02", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07606461663.02"
            ], 
            "type": "Person"
          }, 
          {
            "familyName": "Tirzite", 
            "givenName": "D.", 
            "type": "Person"
          }, 
          {
            "familyName": "Makarova", 
            "givenName": "N.", 
            "id": "sg:person.015046316243.79", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015046316243.79"
            ], 
            "type": "Person"
          }, 
          {
            "familyName": "Dahurs", 
            "givenName": "G.", 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "https://doi.org/10.1016/s0223-5234(96)80009-2", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1011283632"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/s0223-5234(96)80009-2", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1011283632"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0022-2828(90)90083-e", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1016840710"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/lipi.19880901007", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1016943998"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1039/jr9290000750", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1017321151"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/cber.18830160225", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1029069922"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02635693", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1029619074", 
              "https://doi.org/10.1007/bf02635693"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02668958", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1033972730", 
              "https://doi.org/10.1007/bf02668958"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/lipi.19920941110", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1043159748"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/food.19930370121", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1044312104"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0009-3084(92)90090-c", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1044632545"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0009-3084(92)90090-c", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1044632545"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0891-5849(92)90025-c", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1050546039"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0891-5849(92)90025-c", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1050546039"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/ja01180a037", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055779354"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jm00107a001", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055935308"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://app.dimensions.ai/details/publication/pub.1077594416", 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://app.dimensions.ai/details/publication/pub.1078693271", 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "1996-10", 
        "datePublishedReg": "1996-10-01", 
        "description": "The method of Hantzsch was used to synthesize esters and amides of 2,6-dimethyl-4-aryl-1,4-dihydropyridine-3,5-dicarboxylic acid, containing electron donor substituents in the phenyl ring. It was found that in addition to their antioxidant properties, 3,5-diamides and 4-(3\u2032,4\u2032-dioxyphenyl) derivatives have an affinity for model phospholipid membranes.", 
        "genre": "research_article", 
        "id": "sg:pub.10.1007/bf01169228", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1356886", 
            "issn": [
              "0009-3122", 
              "1573-8353"
            ], 
            "name": "Chemistry of Heterocyclic Compounds", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "10", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "32"
          }
        ], 
        "name": "Synthesis of 1,4-dihydropyridine derivatives having an oxy-, alkoxy-, or dimethylaminophenyl substituent in the 4 position, their antioxidant activity, and their binding to phospholipid membranes", 
        "pagination": "1166-1172", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "0c9285435ad6c3b9dfb44598cafabde7cf83ca2febaa1dd901f237871fe954bf"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1007/bf01169228"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1002640617"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1007/bf01169228", 
          "https://app.dimensions.ai/details/publication/pub.1002640617"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-11T13:35", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000370_0000000370/records_46775_00000000.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1007/BF01169228"
      }
    ]
     

    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/bf01169228'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf01169228'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf01169228'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf01169228'


     

    This table displays all metadata directly associated to this object as RDF triples.

    136 TRIPLES      21 PREDICATES      42 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1007/bf01169228 schema:about anzsrc-for:03
    2 anzsrc-for:0306
    3 schema:author Na736e95bc718443d9b3d172c365293e5
    4 schema:citation sg:pub.10.1007/bf02635693
    5 sg:pub.10.1007/bf02668958
    6 https://app.dimensions.ai/details/publication/pub.1077594416
    7 https://app.dimensions.ai/details/publication/pub.1078693271
    8 https://doi.org/10.1002/cber.18830160225
    9 https://doi.org/10.1002/food.19930370121
    10 https://doi.org/10.1002/lipi.19880901007
    11 https://doi.org/10.1002/lipi.19920941110
    12 https://doi.org/10.1016/0009-3084(92)90090-c
    13 https://doi.org/10.1016/0022-2828(90)90083-e
    14 https://doi.org/10.1016/0891-5849(92)90025-c
    15 https://doi.org/10.1016/s0223-5234(96)80009-2
    16 https://doi.org/10.1021/ja01180a037
    17 https://doi.org/10.1021/jm00107a001
    18 https://doi.org/10.1039/jr9290000750
    19 schema:datePublished 1996-10
    20 schema:datePublishedReg 1996-10-01
    21 schema:description The method of Hantzsch was used to synthesize esters and amides of 2,6-dimethyl-4-aryl-1,4-dihydropyridine-3,5-dicarboxylic acid, containing electron donor substituents in the phenyl ring. It was found that in addition to their antioxidant properties, 3,5-diamides and 4-(3′,4′-dioxyphenyl) derivatives have an affinity for model phospholipid membranes.
    22 schema:genre research_article
    23 schema:inLanguage en
    24 schema:isAccessibleForFree false
    25 schema:isPartOf Nba44c438603047c2b6cb1588b2190743
    26 Nfe26827c096c41d6962ba72f41854b9b
    27 sg:journal.1356886
    28 schema:name Synthesis of 1,4-dihydropyridine derivatives having an oxy-, alkoxy-, or dimethylaminophenyl substituent in the 4 position, their antioxidant activity, and their binding to phospholipid membranes
    29 schema:pagination 1166-1172
    30 schema:productId Nb6463b03360d497dbdd5fcf84b0cd019
    31 Ne98996ea87fe4b228f289a715ed05cab
    32 Nfe2e00b2f3dc431f910d713b98595e8e
    33 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002640617
    34 https://doi.org/10.1007/bf01169228
    35 schema:sdDatePublished 2019-04-11T13:35
    36 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    37 schema:sdPublisher N9125a028c37f4541b8a8a75905c1305b
    38 schema:url http://link.springer.com/10.1007/BF01169228
    39 sgo:license sg:explorer/license/
    40 sgo:sdDataset articles
    41 rdf:type schema:ScholarlyArticle
    42 N2d9f9645fab748d4bcdd1c030a960331 schema:familyName Dahurs
    43 schema:givenName G.
    44 rdf:type schema:Person
    45 N408776b7599a47ccb861118c0e7b1f5f rdf:first N821b95635b474dc99bf732184fa50198
    46 rdf:rest Neb5e6950c2454160ae497d4f8e716e56
    47 N821b95635b474dc99bf732184fa50198 schema:familyName Tirzite
    48 schema:givenName D.
    49 rdf:type schema:Person
    50 N9038a4f7f62e48cfab85935d75f91c41 rdf:first sg:person.012211761547.48
    51 rdf:rest Nf494dd6b5f7744e2a88920f7b3a44554
    52 N9125a028c37f4541b8a8a75905c1305b schema:name Springer Nature - SN SciGraph project
    53 rdf:type schema:Organization
    54 Na736e95bc718443d9b3d172c365293e5 rdf:first sg:person.012155141657.93
    55 rdf:rest Ne67906448d95420d8b4b830e3e4e5f5f
    56 Nabba5df014cb4f5fbec7b4ecb27deb19 rdf:first N2d9f9645fab748d4bcdd1c030a960331
    57 rdf:rest rdf:nil
    58 Nb6463b03360d497dbdd5fcf84b0cd019 schema:name doi
    59 schema:value 10.1007/bf01169228
    60 rdf:type schema:PropertyValue
    61 Nba44c438603047c2b6cb1588b2190743 schema:volumeNumber 32
    62 rdf:type schema:PublicationVolume
    63 Ne67906448d95420d8b4b830e3e4e5f5f rdf:first sg:person.01360231013.54
    64 rdf:rest N9038a4f7f62e48cfab85935d75f91c41
    65 Ne98996ea87fe4b228f289a715ed05cab schema:name readcube_id
    66 schema:value 0c9285435ad6c3b9dfb44598cafabde7cf83ca2febaa1dd901f237871fe954bf
    67 rdf:type schema:PropertyValue
    68 Neb5e6950c2454160ae497d4f8e716e56 rdf:first sg:person.015046316243.79
    69 rdf:rest Nabba5df014cb4f5fbec7b4ecb27deb19
    70 Nf494dd6b5f7744e2a88920f7b3a44554 rdf:first sg:person.07606461663.02
    71 rdf:rest N408776b7599a47ccb861118c0e7b1f5f
    72 Nfe26827c096c41d6962ba72f41854b9b schema:issueNumber 10
    73 rdf:type schema:PublicationIssue
    74 Nfe2e00b2f3dc431f910d713b98595e8e schema:name dimensions_id
    75 schema:value pub.1002640617
    76 rdf:type schema:PropertyValue
    77 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
    78 schema:name Chemical Sciences
    79 rdf:type schema:DefinedTerm
    80 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
    81 schema:name Physical Chemistry (incl. Structural)
    82 rdf:type schema:DefinedTerm
    83 sg:journal.1356886 schema:issn 0009-3122
    84 1573-8353
    85 schema:name Chemistry of Heterocyclic Compounds
    86 rdf:type schema:Periodical
    87 sg:person.012155141657.93 schema:familyName Plotnietse
    88 schema:givenName M.
    89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012155141657.93
    90 rdf:type schema:Person
    91 sg:person.012211761547.48 schema:familyName Uldrikis
    92 schema:givenName Ya.
    93 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012211761547.48
    94 rdf:type schema:Person
    95 sg:person.01360231013.54 schema:familyName Tirzitis
    96 schema:givenName G.
    97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01360231013.54
    98 rdf:type schema:Person
    99 sg:person.015046316243.79 schema:familyName Makarova
    100 schema:givenName N.
    101 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015046316243.79
    102 rdf:type schema:Person
    103 sg:person.07606461663.02 schema:familyName Koronova
    104 schema:givenName Zh.
    105 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07606461663.02
    106 rdf:type schema:Person
    107 sg:pub.10.1007/bf02635693 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029619074
    108 https://doi.org/10.1007/bf02635693
    109 rdf:type schema:CreativeWork
    110 sg:pub.10.1007/bf02668958 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033972730
    111 https://doi.org/10.1007/bf02668958
    112 rdf:type schema:CreativeWork
    113 https://app.dimensions.ai/details/publication/pub.1077594416 schema:CreativeWork
    114 https://app.dimensions.ai/details/publication/pub.1078693271 schema:CreativeWork
    115 https://doi.org/10.1002/cber.18830160225 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029069922
    116 rdf:type schema:CreativeWork
    117 https://doi.org/10.1002/food.19930370121 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044312104
    118 rdf:type schema:CreativeWork
    119 https://doi.org/10.1002/lipi.19880901007 schema:sameAs https://app.dimensions.ai/details/publication/pub.1016943998
    120 rdf:type schema:CreativeWork
    121 https://doi.org/10.1002/lipi.19920941110 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043159748
    122 rdf:type schema:CreativeWork
    123 https://doi.org/10.1016/0009-3084(92)90090-c schema:sameAs https://app.dimensions.ai/details/publication/pub.1044632545
    124 rdf:type schema:CreativeWork
    125 https://doi.org/10.1016/0022-2828(90)90083-e schema:sameAs https://app.dimensions.ai/details/publication/pub.1016840710
    126 rdf:type schema:CreativeWork
    127 https://doi.org/10.1016/0891-5849(92)90025-c schema:sameAs https://app.dimensions.ai/details/publication/pub.1050546039
    128 rdf:type schema:CreativeWork
    129 https://doi.org/10.1016/s0223-5234(96)80009-2 schema:sameAs https://app.dimensions.ai/details/publication/pub.1011283632
    130 rdf:type schema:CreativeWork
    131 https://doi.org/10.1021/ja01180a037 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055779354
    132 rdf:type schema:CreativeWork
    133 https://doi.org/10.1021/jm00107a001 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055935308
    134 rdf:type schema:CreativeWork
    135 https://doi.org/10.1039/jr9290000750 schema:sameAs https://app.dimensions.ai/details/publication/pub.1017321151
    136 rdf:type schema:CreativeWork
     




    Preview window. Press ESC to close (or click here)


    ...