eseroline has been researched along with carbamates in 4 studies
*Carbamates: Derivatives of carbamic acid, H2NC(=O)OH. Included under this heading are N-substituted and O-substituted carbamic acids. In general carbamate esters are referred to as urethanes, and polymers that include repeating units of carbamate are referred to as POLYURETHANES. Note however that polyurethanes are derived from the polymerization of ISOCYANATES and the singular term URETHANE refers to the ethyl ester of carbamic acid. [MeSH]
*Carbamates: Derivatives of carbamic acid, H2NC(=O)OH. Included under this heading are N-substituted and O-substituted carbamic acids. In general carbamate esters are referred to as urethanes, and polymers that include repeating units of carbamate are referred to as POLYURETHANES. Note however that polyurethanes are derived from the polymerization of ISOCYANATES and the singular term URETHANE refers to the ethyl ester of carbamic acid. [MeSH]
| Studies (eseroline) | Trials (eseroline) | Recent Studies (post-2010) (eseroline) | Studies (carbamates) | Trials (carbamates) | Recent Studies (post-2010) (carbamates) |
|---|---|---|---|---|---|
| 29 | 0 | 1 | 13,717 | 985 | 4,744 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bartolini, A; Galli, A; Malmberg Aiello, P; Renzi, G | 1 |
| Atack, JR; Brossi, A; Rapoport, SI; Yu, QS | 1 |
| Brossi, A; Greig, NH; Holloway, HW; Yu, Q | 1 |
| Alisaraie, L; Fels, G | 1 |
4 other study(ies) available for eseroline and carbamates
| Article | Year |
|---|---|
In-vitro and in-vivo protection of acetylcholinesterase by eseroline against inactivation by diisopropyl fluorophosphate and carbamates.
Topics: Acetylcholinesterase; Analgesics; Animals; Carbamates; Cholinesterase Reactivators; Indoles; Isoflurophate; Mice | 1985 |
Carbamate analogues of (-)-physostigmine: in vitro inhibition of acetyl- and butyrylcholinesterase.
Topics: Acetylcholinesterase; Animals; Butyrylcholinesterase; Carbamates; Chemical Phenomena; Chemistry; Cholinesterase Inhibitors; Electrophorus; Humans; Indoles; Physostigmine | 1988 |
Syntheses and anticholinesterase activities of (3aS)-N1, N8-bisnorphenserine, (3aS)-N1,N8-bisnorphysostigmine, their antipodal isomers, and other potential metabolites of phenserine.
Topics: Acetylcholinesterase; Butyrylcholinesterase; Carbamates; Cholinesterase Inhibitors; Erythrocytes; Humans; Hydrolysis; In Vitro Techniques; Indoles; Oxidation-Reduction; Phenylcarbamates; Physostigmine; Stereoisomerism; Structure-Activity Relationship | 1998 |
Molecular docking study on the "back door" hypothesis for product clearance in acetylcholinesterase.
Topics: Acetylcholinesterase; Amino Acids; Animals; Binding Sites; Carbamates; Cholinesterase Inhibitors; Computer Simulation; Crystallography, X-Ray; Indoles; Models, Molecular; Protein Structure, Tertiary; Torpedo; Water | 2006 |