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| | Troparil Basic information |
| Product Name: | Troparil | | Synonyms: | 2β-Carbomethoxy-3β-phenyltropane;B-CPT;Troparil;(Exo,exo)-8-methyl-3-phenyl-8-azabicyclo(3.2.1)octane-2-carboxylic acid methyl ester;2-beta-Methoxycarbonyl-3-beta-phenyltropane;8-Azabicyclo(3.2.1)octane-2-carboxylic acid, 8-methyl-3-phenyl-, methyl ester, (exo,exo)-;8-Azabicyclo[3.2.1]octane-2-carboxylicacid, 8-Methyl-3-phenyl-, Methyl ester, (1R,2S,3S,5S)-rel-;(–)-2β-Carbomethoxy-3β-phenyltropane,WIN 35,065-2, orβ-CPT) | | CAS: | 74163-84-1 | | MF: | C16H21NO2 | | MW: | 259.34 | | EINECS: | 200-001-8 | | Product Categories: | | | Mol File: | 74163-84-1.mol |  |
| | Troparil Chemical Properties |
| Boiling point | 350.2±42.0 °C(Predicted) | | density | 1.099±0.06 g/cm3(Predicted) | | pka | 9.95±0.60(Predicted) | | InChI | InChI=1/C16H21NO2/c1-17-12-8-9-14(17)15(16(18)19-2)13(10-12)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3/t12-,13+,14+,15-/s3 | | InChIKey | OMBOXYLBBHNWHL-YRABYYAXNA-N | | SMILES | [C@@]12([H])N(C)[C@@]([H])(CC1)C[C@H](C1=CC=CC=C1)[C@@H]2C(OC)=O |&1:0,4,9,16,r| |
| | Troparil Usage And Synthesis |
| Description | Troparil is a phenyltropane-based dopamine reuptake inhibitor that is derived from methylecgonidine. It is a stimulant drug used in scientific research. The most commonly used form of troparil is the tartrate salt, but the hydrochloride and naphthalenedisulfonate salts are also available, as well as the free base. | | Uses | Troparil is used in scientific research into the dopamine reuptake transporter. 3H-radiolabelled forms of troparil have been used in humans and animals to map the distribution of dopamine transporters in the brain. It is also used for animal research into stimulant drugs as an alternative to cocaine which produces similar effects, but avoids the stringent licensing requirements for the use of cocaine itself. | | Pharmacokinetics | Troparil is a few times more potent than cocaine as a dopamine reuptake inhibitor, but is less potent as a serotonin reuptake inhibitor, and has a duration spanning a few times longer, since the phenyl ring is directly connected to the tropane ring through a non-hydrolyzable carbon-carbon bond. The lack of an ester linkage removes the local anesthetic action from the drug, so troparil is a pure stimulant. This change in activity also makes troparil slightly less cardiotoxic than cocaine. |
| | Troparil Preparation Products And Raw materials |
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