Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C16H21NO2 |
| Molecular Weight | 259.3434 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]1[C@H]2CC[C@@H](C[C@@H]1C3=CC=CC=C3)N2C
InChI
InChIKey=OMBOXYLBBHNWHL-YJNKXOJESA-N
InChI=1S/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-/m0/s1
Approval Year
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WIKIPEDIA |
Designer-drugs-Troparil
Created by
admin on Sat Dec 16 11:23:38 GMT 2023 , Edited by admin on Sat Dec 16 11:23:38 GMT 2023
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170832
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300000042748
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50372-80-0
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AH3LC885W8
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DTXSID30964641
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TROPARIL
Created by
admin on Sat Dec 16 11:23:38 GMT 2023 , Edited by admin on Sat Dec 16 11:23:38 GMT 2023
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PRIMARY | Troparil (also known as (?)-2.beta.-Carbomethoxy-3.beta.-phenyltropane, WIN 35,065-2, or .Beta.-CPT) is a stimulant drug used in scientific research. Troparil is a phenyltropane-based dopamine reuptake inhibitor (DRI) that is derived from methylecgonidine. 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. |
ACTIVE MOIETY
