pyridazine has been researched along with pyrroles in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hayashi, M; Iguchi, Y; Iizuka, K; Kajiwara, I; Kawamura, M; Miyamoto, T; Nakazawa, M; Ohyama, I; Okada, T; Taniguchi, K; Tanouchi, T | 1 |
| Fotsch, C; St Jean, DJ | 1 |
| Lozach, O; Malinka, W; Redzicka, A | 1 |
| Barbosa, SA; Chen, Z; Gullo-Brown, J; Huynh, T; Kim, SH; Leavitt, KJ; Manne, V; Poss, MA; Ricca, CS; Salvati, ME; Tortolani, DR; Vaccaro, W; Wei, DD | 1 |
| Alajarín, R; de Lucio, H; Gago, F; García-Marín, J; García-Soriano, JC; Jiménez-Ruiz, A; Sánchez-Alonso, P; Toro, MÁ; Vaquero, JJ | 1 |
1 review(s) available for pyridazine and pyrroles
| Article | Year |
|---|---|
Mitigating heterocycle metabolism in drug discovery.
Topics: Animals; Biotransformation; Databases, Factual; Drug Discovery; Drug Interactions; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds, 4 or More Rings; Humans; Mice; Pharmaceutical Preparations; Rats | 2012 |
4 other study(ies) available for pyridazine and pyrroles
| Article | Year |
|---|---|
Highly selective inhibitors of thromboxane synthetase. 2. Pyridine derivatives.
Topics: Animals; Oxidoreductases; Pyridines; Sheep; Structure-Activity Relationship; Thromboxane-A Synthase | 1981 |
New derivatives of pyrrolo[3,4-d]pyridazinone and their anticancer effects.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Checkpoint Kinase 1; Chemistry, Pharmaceutical; Drug Screening Assays, Antitumor; France; Humans; Molecular Structure; Protein Kinases; Pyridazines; Pyrroles; Starfish; Structure-Activity Relationship | 2004 |
Pyrrolopyridazine MEK inhibitors.
Topics: Acylation; Amines; Aniline Compounds; Animals; Drug Design; Enzyme Inhibitors; Humans; Mitogen-Activated Protein Kinase Kinases; Pyridazines; Pyrroles; Rats; Structure-Activity Relationship | 2006 |
Pyridazino-pyrrolo-quinoxalinium salts as highly potent and selective leishmanicidal agents targeting trypanothione reductase.
Topics: Antiprotozoal Agents; Dose-Response Relationship, Drug; Enzyme Inhibitors; Humans; Leishmania infantum; Molecular Structure; NADH, NADPH Oxidoreductases; Parasitic Sensitivity Tests; Pyridazines; Pyrroles; Quinoxalines; Salts; Structure-Activity Relationship; THP-1 Cells | 2022 |