pyrroles has been researched along with mannich bases in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (23.08) | 18.7374 |
| 1990's | 1 (7.69) | 18.2507 |
| 2000's | 4 (30.77) | 29.6817 |
| 2010's | 4 (30.77) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Gompertz, J; Messinger, P | 1 |
| Artico, M; Corelli, F; Massa, S; Ortenzi, G; Simonetti, N; Stefancich, G; Strippoli, V | 1 |
| Biava, M; Fioravanti, R; Frachey, G; Mencarelli, P; Perazzi, ME; Porretta, GC; Simonetti, N; Sleiter, G; Villa, A | 1 |
| Antonucci, F; Caparrotta, L; Chiarelotto, G; Ferlin, MG; Froldi, G | 1 |
| Kahan, BD; Podder, H | 1 |
| Handa, S; Harada, S; Matsunaga, S; Shibasaki, M | 1 |
| Thompson, JE | 1 |
| ALBERTSON, NF | 1 |
| Ghorai, D; Jana, D; Kumar, R; Mani, G | 1 |
| Barber, DM; Dixon, DJ; Sanganee, H | 1 |
| Gong, P; Qin, M; Tian, Y; Wang, L; Yan, S; Zhang, H; Zhao, Y | 1 |
| Czyżnikowska, Ż; Gębczak, K; Kochel, A; Redzicka, A; Szczukowski, Ł; Wiatrak, B | 1 |
| Krzyżak, E; Marciniak, A; Peregrym, K; Potyrak, K; Świątek, P; Szczukowski, Ł; Wiatrak, B; Zając, P; Zborowska, A | 1 |
1 review(s) available for pyrroles and mannich bases
| Article | Year |
|---|---|
JAK protein kinase inhibitors.
Topics: Animals; Drug Design; Enzyme Inhibitors; Forecasting; Gene Expression Regulation; Humans; Janus Kinase 1; Janus Kinase 2; Janus Kinase 3; Mannich Bases; Piperidines; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Pyrimidines; Pyrroles; Quinazolines; Signal Transduction; TYK2 Kinase | 2005 |
12 other study(ies) available for pyrroles and mannich bases
| Article | Year |
|---|---|
[Sulfones as chemical carriers of substances with germicid activity, VIII: sulfonyl derivatives of the mannich bases of quinaldine, pyrrole and phenol (author's transl)].
Topics: Bacteria; Chemical Phenomena; Chemistry; Mannich Bases; Phenols; Pyrroles; Quinaldines; Quinolines; Sulfones | 1977 |
[Antibacterial and antifungal agents. IV. Synthesis and antifungal activity of econazole analogs with pyrrole structure].
Topics: Antifungal Agents; Chemical Phenomena; Chemistry; Econazole; Imidazoles; Mannich Bases; Microbial Sensitivity Tests; Pyrroles | 1985 |
Study of the Mannich reaction: beta-amino-methylation of N-aryl and N-azaheteroaryl-substituted 2,5-dimethylpyrroles, compounds with potential biological activity.
Topics: Anti-Bacterial Agents; Anti-Infective Agents; Bacteria; Candida; Chemical Phenomena; Chemistry, Physical; Fungi; Mannich Bases; Pyridines; Pyrimidines; Pyrroles; Thiazoles | 1995 |
Mannich bases of 3H-pyrrolo[3,2-f]quinoline having vasorelaxing activity.
Topics: Animals; Arteries; Dose-Response Relationship, Drug; In Vitro Techniques; Magnetic Resonance Spectroscopy; Male; Mannich Bases; Muscle, Smooth, Vascular; Piperazines; Pyrroles; Quinolines; Rats; Rats, Wistar; Tail; Vasodilation; Vasodilator Agents | 2002 |
Janus kinase 3: a novel target for selective transplant immunosupression.
Topics: Amino Acid Sequence; Animals; Drug Evaluation, Preclinical; Graft Rejection; Humans; Immunosuppressive Agents; Interleukin Receptor Common gamma Subunit; Janus Kinase 2; Janus Kinase 3; Lymphocyte Activation; Lymphocytes; Macaca fascicularis; Mannich Bases; Mice; Molecular Sequence Data; Molecular Structure; Phosphorylation; Prodigiosin; Protein Kinase Inhibitors; Protein Processing, Post-Translational; Protein Structure, Tertiary; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Pyrroles; Rats; Receptors, Cytokine; Receptors, Interleukin-2; Sequence Alignment; Sequence Homology, Amino Acid; Signal Transduction; Substrate Specificity | 2004 |
Direct catalytic asymmetric Mannich-type reactions of N-(2-hydroxyacetyl)pyrrole as an ester-equivalent donor.
Topics: Amino Alcohols; Catalysis; Esters; Mannich Bases; Molecular Structure; Pyrroles | 2005 |
Alkylation with non-ketonic Mannich bases; aminothizoles and pyrrole.
Topics: Alkylation; Mannich Bases; Pyrroles | 1948 |
Azatripyrrolic and azatetrapyrrolic macrocycles from the Mannich reaction of pyrrole: receptors for anions.
Topics: Aza Compounds; Halogens; Macrocyclic Compounds; Mannich Bases; Pyrroles | 2010 |
One-pot nitro-Mannich/hydroamination cascades for the direct synthesis of 2,5-disubstituted pyrroles using base and gold catalysis.
Topics: Amination; Catalysis; Gold; Hydrogen-Ion Concentration; Mannich Bases; Nitro Compounds; Pyrroles | 2011 |
Novel 6-methoxycarbonyl indolinones bearing a pyrrole Mannich base moiety as angiokinase inhibitors.
Topics: Apoptosis; Cell Line, Tumor; Drug Screening Assays, Antitumor; Humans; Indoles; Inhibitory Concentration 50; Mannich Bases; Molecular Docking Simulation; Neovascularization, Pathologic; Protein Kinase Inhibitors; Protein Kinases; Pyrroles; Receptor, Platelet-Derived Growth Factor beta; Vascular Endothelial Growth Factor A | 2017 |
COX-1/COX-2 inhibition activities and molecular docking study of newly designed and synthesized pyrrolo[3,4-c]pyrrole Mannich bases.
Topics: Cells, Cultured; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase Inhibitors; Dose-Response Relationship, Drug; Drug Design; Humans; Mannich Bases; Molecular Docking Simulation; Molecular Structure; Pyrroles; Structure-Activity Relationship | 2019 |
Design, Synthesis and Comprehensive Investigations of Pyrrolo[3,4-
Topics: Antioxidants; Catalytic Domain; Cell Line; Cell Survival; Circular Dichroism; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Drug Design; Female; Fibroblasts; Humans; Inhibitory Concentration 50; Mannich Bases; Middle Aged; Molecular Docking Simulation; Molecular Structure; Oxadiazoles; Pyridazines; Pyrroles; Serum Albumin, Bovine; Structure-Activity Relationship | 2020 |