hyaluronoglucosaminidase has been researched along with n(6)-cyclohexyladenosine in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bressi, JC; Buckner, FS; Choe, J; Gelb, MH; Hol, WG; Hough, MT; Van Voorhis, WC; Verlinde, CL | 1 |
| Cappellacci, L; Franchetti, P; Graser, G; Grifantini, M; Jayaram, HN; Lavecchia, A; Petrelli, R; Saiko, P; Szekeres, T; Vita, P | 1 |
| Drenichev, MS; Karganova, GG; Kozlovskaya, LI; Kurochkin, NN; Mikhailov, SN; Orlov, AA; Oslovsky, VE; Osolodkin, DI; Palyulin, VA; Solyev, PN | 1 |
3 other study(ies) available for hyaluronoglucosaminidase and n(6)-cyclohexyladenosine
| Article | Year |
|---|---|
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 |
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 |
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 |