tiletamine hydrochloride has been researched along with triethylamine in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bennett, JC; Habeeb, AF | 1 |
Gasser, K; Hahin, R; Larsen, J | 1 |
Chen, Q; Chen, T; He, B; Lin, HY; Wang, DW; Wu, FX; Yang, GF; Yang, WC | 1 |
Anisina, YE; Egorov, MP; Elinson, MN; Goloveshkin, AS; Karpenko, KA; Vereshchagin, AN; Zlotin, SG | 1 |
4 other study(ies) available for tiletamine hydrochloride and triethylamine
Article | Year |
---|---|
Obviation of destructive action of 0.2 M NaOH on proteins during arginine modification with cyclohexanedione by use of 0.1 M triethylamine as solvent.
Topics: Arginine; Cyclohexanones; Disulfides; Ethylamines; Humans; Hydrogen-Ion Concentration; Immunoglobulin G; Indicators and Reagents; Kinetics; Lactalbumin; Muramidase; Proteins; Serum Albumin, Bovine; Sodium Hydroxide; Solvents | 1971 |
Predictions of the EC50 for action potential block for aliphatic solutes.
Topics: Action Potentials; Animals; Butanones; Chloroform; Cyclohexanones; Dose-Response Relationship, Drug; Ethylamines; Membrane Fluidity; Muscle Fibers, Skeletal; Patch-Clamp Techniques; Potassium Chloride; Rana pipiens; Sciatic Nerve; Sodium Channel Blockers; Solvents | 2008 |
An Efficient One-Pot Synthesis of 2-(Aryloxyacetyl)cyclohexane-1,3-diones as Herbicidal 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Arabidopsis; Brassica rapa; Cyclohexanones; Dose-Response Relationship, Drug; Enzyme Inhibitors; Ethylamines; Herbicides; Imidazoles; Molecular Structure; Naphthalenes; Nitriles; Plant Weeds; Structure-Activity Relationship; Weed Control; Zea mays | 2016 |
High diastereoselective amine-catalyzed Knoevenagel-Michael-cyclization-ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones.
Topics: Benzaldehydes; Catalysis; Cyclization; Cyclohexanones; Ethylamines; Green Chemistry Technology; Isoxazoles; Quinolines; Stereoisomerism | 2018 |