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Usage

Uses

Used in Scientific Research:
Tropacocaine is employed as a reference standard in scientific research for testing the binding affinity of ligands to dopamine and serotonin receptors. This helps researchers understand the interactions between these ligands and the receptors, which can be crucial for developing new drugs and therapies.
Used in Drug Development:
As a derivative of cocaine with similar pharmacological effects, tropacocaine may have potential applications in drug development. Further research is needed to fully understand its effects, potential benefits, and risks, which could lead to the discovery of new medications or therapeutic approaches.
Used in Controlled Substances Regulation:
Due to its potential for abuse and addiction, tropacocaine is a controlled substance in many countries. Its use is regulated to prevent misuse and ensure that it is only used for legitimate scientific and medical purposes.

InChI:InChI=1/C11H20N2O2/c1-10(2,3)15-9(14)13-7-11-4-8(11)5-12-6-11/h8,12H,4-7H2,1-3H3,(H,13,14)

Relevant academic research and scientific papers

Azabicyclo quinolone carboxylic acids

Quinolone carboxylic acids 7-substituted by azabicyclo groups have antibacterial activity., Antibacterial wherein, R1 is hydrogen, a pharmaceutically acceptable cation, or alkyl;, Y, when taken independently, is ethyl, t-butyl, vinyl, cyclopropyl, 2-fluoroethyl, p-fluorophenyl, or o,p-difluorophenyl;, W is hydrogen, F, Cl, Br, alkyl, alkoxy, NH2, NHCH3;, A is CH, CF, CCl, COCH3, C-CH3, C-CN or N; or, A is carbon and is taken together with Y and the carbon and nitrogen to which A and Y are attached to form a five or six membered ring which may contain oxygen or a double bond, and which may have attached thereto R8 which is methyl or methylene; and, R2 is wherein R3, R4, R5, R6, R7, R9, R10 and R25 are each independently H, CH3, CH2NH2, CH2NHCH3 or CH2NHC2H5, and R5, R6, R7, and R9 may also independently be NH2, NHCH3 or NHC2H5.