P. Bartos, L. Piotrowski, B. Nawrot, G. Pratviel, E. Sochacka
{"title":"The possible pathway of oxone-mediated desulfuration of 2-thiouridine","authors":"P. Bartos, L. Piotrowski, B. Nawrot, G. Pratviel, E. Sochacka","doi":"10.1135/CSS201414163","DOIUrl":"https://doi.org/10.1135/CSS201414163","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"108 1","pages":"163-166"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63712933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
B. Dumat, G. Bordeau, A. Aranda-Pérez, F. Mahuteau-Betzer, C. Fiorini-Debuisschert, M. Teulade‐Fichou
{"title":"Novel triphenylamines optimized for two-photon excited microscopy: from DNA to protein labeling","authors":"B. Dumat, G. Bordeau, A. Aranda-Pérez, F. Mahuteau-Betzer, C. Fiorini-Debuisschert, M. Teulade‐Fichou","doi":"10.1135/CSS201414320","DOIUrl":"https://doi.org/10.1135/CSS201414320","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"320-321"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Petrová, M. Buděšínský, Eva Zborníková, Natalia Panova, Pavel Novák, I. Rosenberg
{"title":"Activation of human RNase L by 5’- C -phosphonate-modified oligoadenylates","authors":"M. Petrová, M. Buděšínský, Eva Zborníková, Natalia Panova, Pavel Novák, I. Rosenberg","doi":"10.1135/CSS201414348","DOIUrl":"https://doi.org/10.1135/CSS201414348","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"348-349"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Preparation of PNA-diamino acid-oligoether conjugates","authors":"Alice Ghidini, Peter Steunenberg, R. Strömberg","doi":"10.1135/CSS201414270","DOIUrl":"https://doi.org/10.1135/CSS201414270","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"270-273"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zofia Tomasiewicz, Marcin Warmiński, K. Ubych, Maciej Lukaszewicz, J. Zuberek, A. Kropiwnicka, E. Darżynkiewicz, J. Kowalska, J. Jemielity
{"title":"Properties and applications of amino- or carboxyfunctionalized mRNA 5’-cap analogues and their conjugates","authors":"Zofia Tomasiewicz, Marcin Warmiński, K. Ubych, Maciej Lukaszewicz, J. Zuberek, A. Kropiwnicka, E. Darżynkiewicz, J. Kowalska, J. Jemielity","doi":"10.1135/CSS201414387","DOIUrl":"https://doi.org/10.1135/CSS201414387","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"387-388"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713623","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zhinan Jin, J. Deval, J. Symons, Hua Tan, K. Shaw, Hyunsoon Kang, C. Moy, D. Smith, Guangyi Wang, N. Dyatkina, L. Blatt, L. Beigelman
{"title":"Derisking the potential for mitochondrial toxicity of ribonucleoside analogs in antiviral screens","authors":"Zhinan Jin, J. Deval, J. Symons, Hua Tan, K. Shaw, Hyunsoon Kang, C. Moy, D. Smith, Guangyi Wang, N. Dyatkina, L. Blatt, L. Beigelman","doi":"10.1135/CSS201414123","DOIUrl":"https://doi.org/10.1135/CSS201414123","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"123-125"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63712711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
D. Cirule, K. Ozols, Irina Novosjolova, M. Turks, Ē. Bizdēna
{"title":"A Synthetic Route to 2,6-Bis-triazolyl Purine Deoxynucleosides via Click Chemistry","authors":"D. Cirule, K. Ozols, Irina Novosjolova, M. Turks, Ē. Bizdēna","doi":"10.1135/CSS201414233","DOIUrl":"https://doi.org/10.1135/CSS201414233","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"233-235"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63712972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tobias Santner, Lukas Rigger, S. Flür, V. Schwarz, M. Košutić, J. Levic, L. Jud, Marina Frener, Sandro Neuner, R. Micura
{"title":"From novel RNA modifications to riboswitch function","authors":"Tobias Santner, Lukas Rigger, S. Flür, V. Schwarz, M. Košutić, J. Levic, L. Jud, Marina Frener, Sandro Neuner, R. Micura","doi":"10.1135/CSS201414183","DOIUrl":"https://doi.org/10.1135/CSS201414183","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"183-185"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
D. Hocková, D. Keough, P. Spacek, Z. Janeba, M. Edstein, M. Chavchich, Tzu-Hsuan Wang, W. Eng, N. West, J. Jersey, L. Guddat
{"title":"Acyclic nucleoside bisphosphonates as inhibitors of 6-oxopurine phosphoribosyltransferases: potential antimalarial and antibacterial agents","authors":"D. Hocková, D. Keough, P. Spacek, Z. Janeba, M. Edstein, M. Chavchich, Tzu-Hsuan Wang, W. Eng, N. West, J. Jersey, L. Guddat","doi":"10.1135/CSS201414107","DOIUrl":"https://doi.org/10.1135/CSS201414107","url":null,"abstract":"","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"14 1","pages":"107-110"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Functionalized nucleic acids have found applications in chemical biology, bioanalysis, catalysis and nanotechnology. Modifications can be introduced into the phosphate backbone, sugar moiety and, most often, onto a nucleobase. Base-modified DNA can be synthesized chemically or enzymatically. Chemical synthesis is carried out on solid support and utilizes phosphorimidate building blocks. Enzymatic synthesis of (base-modified) DNA is based on the incorporation of (functionalized) nucleoside triphosphates by a DNA polymerase.
{"title":"Preparation of modified oligonucleotides by nicking enzyme amplification reaction","authors":"Petra Ménová, Michal Hocek","doi":"10.1135/CSS201414324","DOIUrl":"https://doi.org/10.1135/CSS201414324","url":null,"abstract":" Functionalized nucleic acids have found applications in chemical biology, bioanalysis, catalysis and nanotechnology. Modifications can be introduced into the phosphate backbone, sugar moiety and, most often, onto a nucleobase. Base-modified DNA can be synthesized chemically or enzymatically. Chemical synthesis is carried out on solid support and utilizes phosphorimidate building blocks. Enzymatic synthesis of (base-modified) DNA is based on the incorporation of (functionalized) nucleoside triphosphates by a DNA polymerase.","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"33 1","pages":"324-325"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63713271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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