Page last updated: 2024-08-22

hyaluronoglucosaminidase and n(6)-phenyladenosine

hyaluronoglucosaminidase has been researched along with n(6)-phenyladenosine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Daly, DT; Kusachi, S; Olsson, RA; Thompson, RD; Yamada, N1
Buolamwini, JK; Zhu, Z1
Cappellacci, L; Franchetti, P; Graser, G; Grifantini, M; Jayaram, HN; Lavecchia, A; Petrelli, R; Saiko, P; Szekeres, T; Vita, P1
Chizhov, AO; Drenichev, MS; Kurochkin, NN; Leyssen, P; Mikhailov, SN; Neyts, J; Oslovsky, VE; Pannecouque, C; Sun, L; Tararov, VI; Tijsma, A1

Other Studies

4 other study(ies) available for hyaluronoglucosaminidase and n(6)-phenyladenosine

ArticleYear
Dog coronary artery adenosine receptor: structure of the N6-aryl subregion.
    Journal of medicinal chemistry, 1986, Volume: 29, Issue:6

    Topics: Adenosine; Animals; Coronary Vessels; Dogs; Models, Structural; Protein Binding; Receptors, Cell Surface; Receptors, Purinergic; Serum Albumin; Structure-Activity Relationship

1986
Constrained NBMPR analogue synthesis, pharmacophore mapping and 3D-QSAR modeling of equilibrative nucleoside transporter 1 (ENT1) inhibitory activity.
    Bioorganic & medicinal chemistry, 2008, Apr-01, Volume: 16, Issue:7

    Topics: Drug Design; Equilibrative Nucleoside Transporter 1; Glycosides; Humans; K562 Cells; Models, Biological; Models, Molecular; Molecular Structure; Quantitative Structure-Activity Relationship; Static Electricity; Thioinosine

2008
Ribose-modified purine nucleosides as ribonucleotide reductase inhibitors. Synthesis, antitumor activity, and molecular modeling of N6-substituted 3'-C-methyladenosine derivatives.
    Journal of medicinal chemistry, 2008, Jul-24, Volume: 51, Issue:14

    Topics: Adenosine; Antineoplastic Agents; Cell Line, Tumor; Enzyme Inhibitors; Humans; Ribonucleotide Reductases; Ribose; Structure-Activity Relationship

2008
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