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contentType Journal Article|Research Support, Non-U.S. Gov't
endingPage 302
issn 0223-5234
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publicationName European Journal of Medicinal Chemistry
startingPage 288
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bibliographicCitation Stipković Babić M, Makuc D, Plavec J, Martinović T, Kraljević Pavelić S, Pavelić K, Snoeck R, Andrei G, Schols D, Wittine K, Mintas M. Novel halogenated 3-deazapurine, 7-deazapurine and alkylated 9-deazapurine derivatives of l-ascorbic or imino-l-ascorbic acid: Synthesis, antitumour and antiviral activity evaluations. European Journal of Medicinal Chemistry. 2015 Sep;102():288–302. doi: 10.1016/j.ejmech.2015.08.008.
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date 2015-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC7125971
https://pubmed.ncbi.nlm.nih.gov/26291038
https://doi.org/10.1016/j.ejmech.2015.08.008
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https://portal.issn.org/resource/ISSN/0223-5234
language English
source https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/
title Novel halogenated 3-deazapurine, 7-deazapurine and alkylated 9-deazapurine derivatives of l-ascorbic or imino-l-ascorbic acid: Synthesis, antitumour and antiviral activity evaluations
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http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394000_AID1252410_PMID26291038_VALUE1
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103619996_AID1252405_PMID26291038_VALUE1
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394002_AID1252393_PMID26291038_VALUE10
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394005_AID1252393_PMID26291038_VALUE13
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394001_AID1252402_PMID26291038_VALUE5
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394001_AID1252404_PMID26291038_VALUE5
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394114_AID1252390_PMID26291038_VALUE19
http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID318394009_AID1252388_PMID26291038_VALUE17

Total number of triples: 236.