hyaluronoglucosaminidase has been researched along with n(6)-benzyladenosine in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 4 (44.44) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Daly, DT; Kusachi, S; Olsson, RA; Thompson, RD; Yamada, N | 1 |
| Cristalli, G; Esker, JL; Jacobson, KA; Ji, XD; Melman, N; Olah, ME; Schneller, SW; Secrist, JA; Siddiqi, SM; Tiwari, KN | 1 |
| Bressi, JC; Buckner, FS; Choe, J; Gelb, MH; Hol, WG; Hough, MT; Van Voorhis, WC; Verlinde, CL | 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 |
| Brizzolari, A; Faioni, E; Razzari, C; Santaniello, E; Vistoli, G | 1 |
| Chizhov, AO; Drenichev, MS; Kurochkin, NN; Leyssen, P; Mikhailov, SN; Neyts, J; Oslovsky, VE; Pannecouque, C; Sun, L; Tararov, VI; Tijsma, A | 1 |
| Drenichev, MS; Karganova, GG; Kozlovskaya, LI; Kurochkin, NN; Mikhailov, SN; Orlov, AA; Oslovsky, VE; Osolodkin, DI; Palyulin, VA; Solyev, PN | 1 |
| Béres, T; Dolezal, K; Dzubák, P; Hajdúch, M; Krystof, V; Lenobel, R; Niemann, P; Spíchal, L; Strnad, M; Voller, J; Zatloukal, M | 1 |
9 other study(ies) available for hyaluronoglucosaminidase and n(6)-benzyladenosine
| 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 |
Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors.
Topics: Adenosine; Animals; Cell Membrane; CHO Cells; Corpus Striatum; Cricetinae; In Vitro Techniques; Magnetic Resonance Spectroscopy; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Purines; Radioligand Assay; Rats; Recombinant Proteins; Ribose; Structure-Activity Relationship | 1995 |
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine.
Topics: Adenosine; Animals; Combinatorial Chemistry Techniques; Crystallography, X-Ray; Enzyme Inhibitors; Glyceraldehyde-3-Phosphate Dehydrogenases; Glycerolphosphate Dehydrogenase; Models, Molecular; Molecular Conformation; Phosphoglycerate Kinase; Protein Binding; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei brucei; Trypanosoma cruzi | 2000 |
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 |
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.
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.
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.
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.
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 |