Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-11

AUTHORS

A. S. Kaledina, A. D. Zorina, V. V. Zarubaev, V. V. Anokhina, E. B. Erkhitueva, R. E. Trifonov

ABSTRACT

Cyanoethylation of dammaran-3β-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-О-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.

PAGES

1627-1632

References to SciGraph publications

  • 2004-03. Synthesis and Pharmacological Activity of Acylated Betulonic Acid Oxides and 28-Oxo-Allobetulone in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2003-05. Synthesis and Antiviral Activity of Hydrazides and Substituted Benzalhydrazides of Betulinic Acid and Its Derivatives in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2010-07. Antiviral activity of 2,3-secotriterpenic hydrazones of the lupane and 19β,28-epoxy-18α-oleanane types in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2009-01. Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2011-05. Synthesis and antitumor activity of aminopropoxy derivatives of betulin, erythrodiol, and uvaol in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2010-11. Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 1997-06. Synthesis of secoacids of the damarrane series in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2013-03. Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus in CHEMISTRY OF NATURAL COMPOUNDS
  • 2007-11. Effect of nitrogen-containing derivatives of the plant triterpenes betulin and glycyrrhetic acid on the growth of MT-4, MOLT-4, CEM, and Hep G2 tumor cells in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2006-04. Polymeric derivatives of dipterocarpol, a dammarane triterpenoid in RUSSIAN JOURNAL OF APPLIED CHEMISTRY
  • 2011-09. Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2010-05. Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids in RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY
  • 2011-04. Synthetic transformations of higher terpenoids: XXIV. Synthesis of cyanoethyl derivatives of lupane triterpenoids and their transformation into 1,2,4-oxadiazoles in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s1070428015110184

    DOI

    http://dx.doi.org/10.1134/s1070428015110184

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1021256340


    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/2008/0904", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Chemical Engineering", 
            "type": "DefinedTerm"
          }, 
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/09", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Engineering", 
            "type": "DefinedTerm"
          }
        ], 
        "author": [
          {
            "affiliation": {
              "alternateName": "Saint Petersburg State University", 
              "id": "https://www.grid.ac/institutes/grid.15447.33", 
              "name": [
                "St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Kaledina", 
            "givenName": "A. S.", 
            "id": "sg:person.015364461455.56", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015364461455.56"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Saint Petersburg State University", 
              "id": "https://www.grid.ac/institutes/grid.15447.33", 
              "name": [
                "St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Zorina", 
            "givenName": "A. D.", 
            "id": "sg:person.014157301757.37", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014157301757.37"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Research Institute of Influenza", 
              "id": "https://www.grid.ac/institutes/grid.452514.3", 
              "name": [
                "Research Institute of Influenza, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Zarubaev", 
            "givenName": "V. V.", 
            "id": "sg:person.01030233666.29", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01030233666.29"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Saint Petersburg State University", 
              "id": "https://www.grid.ac/institutes/grid.15447.33", 
              "name": [
                "St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Anokhina", 
            "givenName": "V. V.", 
            "id": "sg:person.0764242132.26", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0764242132.26"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Saint Petersburg State University", 
              "id": "https://www.grid.ac/institutes/grid.15447.33", 
              "name": [
                "St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Erkhitueva", 
            "givenName": "E. B.", 
            "id": "sg:person.010061675145.67", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010061675145.67"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Saint Petersburg State University", 
              "id": "https://www.grid.ac/institutes/grid.15447.33", 
              "name": [
                "St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Trifonov", 
            "givenName": "R. E.", 
            "id": "sg:person.016240375135.66", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016240375135.66"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "sg:pub.10.1134/s1070428011040208", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1007721402", 
              "https://doi.org/10.1134/s1070428011040208"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02464128", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1010253795", 
              "https://doi.org/10.1007/bf02464128"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02464128", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1010253795", 
              "https://doi.org/10.1007/bf02464128"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/j.bmcl.2009.02.122", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1013030643"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/cbdv.201000107", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1015017717"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162011030101", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1016750820", 
              "https://doi.org/10.1134/s1068162011030101"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s107042720604029x", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1017733605", 
              "https://doi.org/10.1134/s107042720604029x"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/0040-4020(58)80024-1", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1020013086"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/s0960-894x(03)00714-5", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1023983764"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/s0960-894x(03)00714-5", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1023983764"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s10600-013-0505-4", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1024737665", 
              "https://doi.org/10.1007/s10600-013-0505-4"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/a:1023948919315", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1026263269", 
              "https://doi.org/10.1023/a:1023948919315"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1351/pac199971061045", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1026916336"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/j.molmed.2004.11.001", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1029067180"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162011050086", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1035560443", 
              "https://doi.org/10.1134/s1068162011050086"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162010030155", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1038105372", 
              "https://doi.org/10.1134/s1068162010030155"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162010030155", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1038105372", 
              "https://doi.org/10.1134/s1068162010030155"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162007060076", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1043330650", 
              "https://doi.org/10.1134/s1068162007060076"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162010060142", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1045498606", 
              "https://doi.org/10.1134/s1068162010060142"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162010060142", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1045498606", 
              "https://doi.org/10.1134/s1068162010060142"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/b:phac.0000034305.96047.87", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1048313155", 
              "https://doi.org/10.1023/b:phac.0000034305.96047.87"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162009010154", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1050126775", 
              "https://doi.org/10.1134/s1068162009010154"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/j.bmcl.2010.12.035", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1051206620"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1068162010040114", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1053060786", 
              "https://doi.org/10.1134/s1068162010040114"
            ], 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2015-11", 
        "datePublishedReg": "2015-11-01", 
        "description": "Cyanoethylation of dammaran-3\u03b2-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-\u041e-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.", 
        "genre": "research_article", 
        "id": "sg:pub.10.1134/s1070428015110184", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": true, 
        "isPartOf": [
          {
            "id": "sg:journal.1136317", 
            "issn": [
              "1070-4280", 
              "1608-3393"
            ], 
            "name": "Russian Journal of Organic Chemistry", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "11", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "51"
          }
        ], 
        "name": "Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids", 
        "pagination": "1627-1632", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "6546b45fd41edf8441ecc10d04c10afcead6239870974b9b78b53a1fbfefd345"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1134/s1070428015110184"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1021256340"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1134/s1070428015110184", 
          "https://app.dimensions.ai/details/publication/pub.1021256340"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-10T15:12", 
        "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/v90/0000000001_0000000264/records_8663_00000585.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1134%2FS1070428015110184"
      }
    ]
     

    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.10.1134/s1070428015110184'

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

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1134/s1070428015110184'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428015110184'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428015110184'


     

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

    172 TRIPLES      21 PREDICATES      47 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1134/s1070428015110184 schema:about anzsrc-for:09
    2 anzsrc-for:0904
    3 schema:author Ne5e4c0f10dc040bf8a86cfd7f63dc854
    4 schema:citation sg:pub.10.1007/bf02464128
    5 sg:pub.10.1007/s10600-013-0505-4
    6 sg:pub.10.1023/a:1023948919315
    7 sg:pub.10.1023/b:phac.0000034305.96047.87
    8 sg:pub.10.1134/s1068162007060076
    9 sg:pub.10.1134/s1068162009010154
    10 sg:pub.10.1134/s1068162010030155
    11 sg:pub.10.1134/s1068162010040114
    12 sg:pub.10.1134/s1068162010060142
    13 sg:pub.10.1134/s1068162011030101
    14 sg:pub.10.1134/s1068162011050086
    15 sg:pub.10.1134/s107042720604029x
    16 sg:pub.10.1134/s1070428011040208
    17 https://doi.org/10.1002/cbdv.201000107
    18 https://doi.org/10.1016/0040-4020(58)80024-1
    19 https://doi.org/10.1016/j.bmcl.2009.02.122
    20 https://doi.org/10.1016/j.bmcl.2010.12.035
    21 https://doi.org/10.1016/j.molmed.2004.11.001
    22 https://doi.org/10.1016/s0960-894x(03)00714-5
    23 https://doi.org/10.1351/pac199971061045
    24 schema:datePublished 2015-11
    25 schema:datePublishedReg 2015-11-01
    26 schema:description Cyanoethylation of dammaran-3β-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-О-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.
    27 schema:genre research_article
    28 schema:inLanguage en
    29 schema:isAccessibleForFree true
    30 schema:isPartOf N22877a27e2424aacaffd7e8a62659b7b
    31 N3e5e64c358034e07ad52a53b3bfd6ef1
    32 sg:journal.1136317
    33 schema:name Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids
    34 schema:pagination 1627-1632
    35 schema:productId N212ba6906ee84dbeb480acfc87f8c718
    36 N430484ceb92c45e5a8d2640b04d7f07d
    37 Nad023769bb8746948d85fe6154988a3b
    38 schema:sameAs https://app.dimensions.ai/details/publication/pub.1021256340
    39 https://doi.org/10.1134/s1070428015110184
    40 schema:sdDatePublished 2019-04-10T15:12
    41 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    42 schema:sdPublisher Nd58b71ac33cb4511a61dc27abe18b25b
    43 schema:url http://link.springer.com/10.1134%2FS1070428015110184
    44 sgo:license sg:explorer/license/
    45 sgo:sdDataset articles
    46 rdf:type schema:ScholarlyArticle
    47 N1065580812ae47ffbce9a3c88db613ba rdf:first sg:person.0764242132.26
    48 rdf:rest N8b5bfdf0c5364599a646631205123bf6
    49 N142e250dc0464400bb6243962a56d7e9 rdf:first sg:person.016240375135.66
    50 rdf:rest rdf:nil
    51 N16488787dd8d44419055617223316a7b rdf:first sg:person.014157301757.37
    52 rdf:rest N23b8b018b2c74b4ab2af92d78ddf8b2f
    53 N212ba6906ee84dbeb480acfc87f8c718 schema:name doi
    54 schema:value 10.1134/s1070428015110184
    55 rdf:type schema:PropertyValue
    56 N22877a27e2424aacaffd7e8a62659b7b schema:issueNumber 11
    57 rdf:type schema:PublicationIssue
    58 N23b8b018b2c74b4ab2af92d78ddf8b2f rdf:first sg:person.01030233666.29
    59 rdf:rest N1065580812ae47ffbce9a3c88db613ba
    60 N3e5e64c358034e07ad52a53b3bfd6ef1 schema:volumeNumber 51
    61 rdf:type schema:PublicationVolume
    62 N430484ceb92c45e5a8d2640b04d7f07d schema:name readcube_id
    63 schema:value 6546b45fd41edf8441ecc10d04c10afcead6239870974b9b78b53a1fbfefd345
    64 rdf:type schema:PropertyValue
    65 N8b5bfdf0c5364599a646631205123bf6 rdf:first sg:person.010061675145.67
    66 rdf:rest N142e250dc0464400bb6243962a56d7e9
    67 Nad023769bb8746948d85fe6154988a3b schema:name dimensions_id
    68 schema:value pub.1021256340
    69 rdf:type schema:PropertyValue
    70 Nd58b71ac33cb4511a61dc27abe18b25b schema:name Springer Nature - SN SciGraph project
    71 rdf:type schema:Organization
    72 Ne5e4c0f10dc040bf8a86cfd7f63dc854 rdf:first sg:person.015364461455.56
    73 rdf:rest N16488787dd8d44419055617223316a7b
    74 anzsrc-for:09 schema:inDefinedTermSet anzsrc-for:
    75 schema:name Engineering
    76 rdf:type schema:DefinedTerm
    77 anzsrc-for:0904 schema:inDefinedTermSet anzsrc-for:
    78 schema:name Chemical Engineering
    79 rdf:type schema:DefinedTerm
    80 sg:journal.1136317 schema:issn 1070-4280
    81 1608-3393
    82 schema:name Russian Journal of Organic Chemistry
    83 rdf:type schema:Periodical
    84 sg:person.010061675145.67 schema:affiliation https://www.grid.ac/institutes/grid.15447.33
    85 schema:familyName Erkhitueva
    86 schema:givenName E. B.
    87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010061675145.67
    88 rdf:type schema:Person
    89 sg:person.01030233666.29 schema:affiliation https://www.grid.ac/institutes/grid.452514.3
    90 schema:familyName Zarubaev
    91 schema:givenName V. V.
    92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01030233666.29
    93 rdf:type schema:Person
    94 sg:person.014157301757.37 schema:affiliation https://www.grid.ac/institutes/grid.15447.33
    95 schema:familyName Zorina
    96 schema:givenName A. D.
    97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014157301757.37
    98 rdf:type schema:Person
    99 sg:person.015364461455.56 schema:affiliation https://www.grid.ac/institutes/grid.15447.33
    100 schema:familyName Kaledina
    101 schema:givenName A. S.
    102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015364461455.56
    103 rdf:type schema:Person
    104 sg:person.016240375135.66 schema:affiliation https://www.grid.ac/institutes/grid.15447.33
    105 schema:familyName Trifonov
    106 schema:givenName R. E.
    107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016240375135.66
    108 rdf:type schema:Person
    109 sg:person.0764242132.26 schema:affiliation https://www.grid.ac/institutes/grid.15447.33
    110 schema:familyName Anokhina
    111 schema:givenName V. V.
    112 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0764242132.26
    113 rdf:type schema:Person
    114 sg:pub.10.1007/bf02464128 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010253795
    115 https://doi.org/10.1007/bf02464128
    116 rdf:type schema:CreativeWork
    117 sg:pub.10.1007/s10600-013-0505-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1024737665
    118 https://doi.org/10.1007/s10600-013-0505-4
    119 rdf:type schema:CreativeWork
    120 sg:pub.10.1023/a:1023948919315 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026263269
    121 https://doi.org/10.1023/a:1023948919315
    122 rdf:type schema:CreativeWork
    123 sg:pub.10.1023/b:phac.0000034305.96047.87 schema:sameAs https://app.dimensions.ai/details/publication/pub.1048313155
    124 https://doi.org/10.1023/b:phac.0000034305.96047.87
    125 rdf:type schema:CreativeWork
    126 sg:pub.10.1134/s1068162007060076 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043330650
    127 https://doi.org/10.1134/s1068162007060076
    128 rdf:type schema:CreativeWork
    129 sg:pub.10.1134/s1068162009010154 schema:sameAs https://app.dimensions.ai/details/publication/pub.1050126775
    130 https://doi.org/10.1134/s1068162009010154
    131 rdf:type schema:CreativeWork
    132 sg:pub.10.1134/s1068162010030155 schema:sameAs https://app.dimensions.ai/details/publication/pub.1038105372
    133 https://doi.org/10.1134/s1068162010030155
    134 rdf:type schema:CreativeWork
    135 sg:pub.10.1134/s1068162010040114 schema:sameAs https://app.dimensions.ai/details/publication/pub.1053060786
    136 https://doi.org/10.1134/s1068162010040114
    137 rdf:type schema:CreativeWork
    138 sg:pub.10.1134/s1068162010060142 schema:sameAs https://app.dimensions.ai/details/publication/pub.1045498606
    139 https://doi.org/10.1134/s1068162010060142
    140 rdf:type schema:CreativeWork
    141 sg:pub.10.1134/s1068162011030101 schema:sameAs https://app.dimensions.ai/details/publication/pub.1016750820
    142 https://doi.org/10.1134/s1068162011030101
    143 rdf:type schema:CreativeWork
    144 sg:pub.10.1134/s1068162011050086 schema:sameAs https://app.dimensions.ai/details/publication/pub.1035560443
    145 https://doi.org/10.1134/s1068162011050086
    146 rdf:type schema:CreativeWork
    147 sg:pub.10.1134/s107042720604029x schema:sameAs https://app.dimensions.ai/details/publication/pub.1017733605
    148 https://doi.org/10.1134/s107042720604029x
    149 rdf:type schema:CreativeWork
    150 sg:pub.10.1134/s1070428011040208 schema:sameAs https://app.dimensions.ai/details/publication/pub.1007721402
    151 https://doi.org/10.1134/s1070428011040208
    152 rdf:type schema:CreativeWork
    153 https://doi.org/10.1002/cbdv.201000107 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015017717
    154 rdf:type schema:CreativeWork
    155 https://doi.org/10.1016/0040-4020(58)80024-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020013086
    156 rdf:type schema:CreativeWork
    157 https://doi.org/10.1016/j.bmcl.2009.02.122 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013030643
    158 rdf:type schema:CreativeWork
    159 https://doi.org/10.1016/j.bmcl.2010.12.035 schema:sameAs https://app.dimensions.ai/details/publication/pub.1051206620
    160 rdf:type schema:CreativeWork
    161 https://doi.org/10.1016/j.molmed.2004.11.001 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029067180
    162 rdf:type schema:CreativeWork
    163 https://doi.org/10.1016/s0960-894x(03)00714-5 schema:sameAs https://app.dimensions.ai/details/publication/pub.1023983764
    164 rdf:type schema:CreativeWork
    165 https://doi.org/10.1351/pac199971061045 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026916336
    166 rdf:type schema:CreativeWork
    167 https://www.grid.ac/institutes/grid.15447.33 schema:alternateName Saint Petersburg State University
    168 schema:name St. Petersburg State University, Universitetskaya nab. 7/9, 199034, St. Petersburg, Russia
    169 rdf:type schema:Organization
    170 https://www.grid.ac/institutes/grid.452514.3 schema:alternateName Research Institute of Influenza
    171 schema:name Research Institute of Influenza, St. Petersburg, Russia
    172 rdf:type schema:Organization
     




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


    ...