hyaluronoglucosaminidase has been researched along with n(6)-phenyladenosine in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Daly, DT; Kusachi, S; Olsson, RA; Thompson, RD; Yamada, N | 1 |
Buolamwini, JK; Zhu, Z | 1 |
Cappellacci, L; Franchetti, P; Graser, G; Grifantini, M; Jayaram, HN; Lavecchia, A; Petrelli, R; Saiko, P; Szekeres, T; Vita, P | 1 |
Chizhov, AO; Drenichev, MS; Kurochkin, NN; Leyssen, P; Mikhailov, SN; Neyts, J; Oslovsky, VE; Pannecouque, C; Sun, L; Tararov, VI; Tijsma, A | 1 |
4 other study(ies) available for hyaluronoglucosaminidase and n(6)-phenyladenosine
Article | Year |
---|---|
Dog coronary artery adenosine receptor: structure of the N6-aryl subregion.
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.
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.
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.
Topics: Adenosine; Antiviral Agents; Dose-Response Relationship, Drug; Enterovirus A, Human; Humans; Microbial Sensitivity Tests; Molecular Structure; Structure-Activity Relationship | 2016 |