Compounds > hyaluronoglucosaminidase
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hyaluronoglucosaminidase and isopentenyladenosine

hyaluronoglucosaminidase has been researched along with isopentenyladenosine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brizzolari, A; Faioni, E; Razzari, C; Santaniello, E; Vistoli, G1
Chizhov, AO; Drenichev, MS; Kurochkin, NN; Leyssen, P; Mikhailov, SN; Neyts, J; Oslovsky, VE; Pannecouque, C; Sun, L; Tararov, VI; Tijsma, A1
Drenichev, MS; Karganova, GG; Kozlovskaya, LI; Kurochkin, NN; Mikhailov, SN; Orlov, AA; Oslovsky, VE; Osolodkin, DI; Palyulin, VA; Solyev, PN1
Béres, T; Dolezal, K; Dzubák, P; Hajdúch, M; Krystof, V; Lenobel, R; Niemann, P; Spíchal, L; Strnad, M; Voller, J; Zatloukal, M1
Béres, T; Doležal, K; Džubák, P; Hajdúch, M; Kaminski, PA; Niemann, P; Strnad, M; Voller, J; Zatloukal, M1

Other Studies

5 other study(ies) available for hyaluronoglucosaminidase and isopentenyladenosine

ArticleYear
Naturally occurring N(6)-substituted adenosines (cytokinin ribosides) are in vitro inhibitors of platelet aggregation: an in silico evaluation of their interaction with the P2Y(12) receptor.
    Bioorganic & medicinal chemistry letters, 2014, Dec-15, Volume: 24, Issue:24

    Topics: Adenosine; Adenosine Diphosphate; Blood Platelets; Cytokinins; Humans; In Vitro Techniques; Plant Growth Regulators; Platelet Aggregation; Platelet Aggregation Inhibitors; Purinergic P1 Receptor Agonists; Receptors, Purinergic P2Y12; Ribonucleosides

2014
Modification of the length and structure of the linker of N(6)-benzyladenosine modulates its selective antiviral activity against enterovirus 71.
    European journal of medicinal chemistry, 2016, Mar-23, Volume: 111

    Topics: Adenosine; Antiviral Agents; Dose-Response Relationship, Drug; Enterovirus A, Human; Humans; Microbial Sensitivity Tests; Molecular Structure; Structure-Activity Relationship

2016
New tools in nucleoside toolbox of tick-borne encephalitis virus reproduction inhibitors.
    Bioorganic & medicinal chemistry letters, 2017, 03-01, Volume: 27, Issue:5

    Topics: Animals; Antiviral Agents; Encephalitis Viruses, Tick-Borne; Humans; Molecular Structure; Nucleosides; Structure-Activity Relationship; Virus Internalization; Virus Replication

2017
Anticancer activity of natural cytokinins: a structure-activity relationship study.
    Phytochemistry, 2010, Volume: 71, Issue:11-12

    Topics: Adenosine; Antineoplastic Agents; Cytokinins; Drug Screening Assays, Antitumor; Genes, p53; Humans; Inhibitory Concentration 50; Isopentenyladenosine; Kinetin; Molecular Structure; National Cancer Institute (U.S.); Plant Growth Regulators; Stereoisomerism; Structure-Activity Relationship; United States

2010
The natural cytokinin 2OH3MeOBAR induces cell death by a mechanism that is different from that of the "classical" cytokinin ribosides.
    Phytochemistry, 2017, Volume: 136

    Topics: Adenosine; Apoptosis; Cell Death; Cytokinins; Glycosides; Isopentenyladenosine; Kinetin; Molecular Structure

2017