BTCP HCL
BTCP HCL Basic information
- Product Name:
- BTCP HCL
- Synonyms:
-
- BTCP HCL
- 1-(1-benzo(b)thien-2-ylcyclohexyl)-piperidin
- 1-(1-benzo(b)thien-2-ylcyclohexyl)piperidine
- gk13
- BTCP HYDROCHLORIDE POTENT & SELECTIVE DO
- 1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine
- N-[1-(Benzo[b]thien-2-yl-cyclohexyl)]piperidine hydrochloride
- 1-(1-Benzo[b]thiophen-2-ylcyclohexyl)piperidine
- CAS:
- 112726-66-6
- MF:
- C19H25NS
- MW:
- 299.47
- Mol File:
- 112726-66-6.mol
BTCP HCL Chemical Properties
- Melting point:
- 80℃ (ethanol )
- Boiling point:
- 425.4±20.0 °C(Predicted)
- Density
- 1.135±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- H2O: >180 mg/mL
- form
- solid
- pka
- 8.56±0.20(Predicted)
- color
- white
BTCP HCL Usage And Synthesis
Uses
Benzothiophenylcyclohexylpiperidine Maleate is a potent dopamine re-uptake/transport inhibitor different from PCP and other stimulants.
Definition
ChEBI: A tertiary amino compound that consists of cyclohexane having piperidin-1-yl and benzothiophen-2-yl groups attached at position 1. A potent dopamine re-uptake inhibitor with a behavioral profile different from that of phencyclidine (PCP) and similar to tha of cocaine.
Biological Activity
A potent dopamine re-uptake inhibitor with a behavioral profile different from that of PCP and similar to that of cocaine.
References
[1] vignon j, pinet v, cerruti c, et al. [3h] n-[1-(2-benzo (b) thiophenyl) cycohexyl] piperidine ([3h] btcp): a new phencyclidine analog selective for the dopamine uptake complex[j]. european journal of pharmacology, 1988, 148(3): 427-436.
[2] chaudieu i, vignon j, chicheportiche m, et al. role of the aromatic group in the inhibition of phencyclidine binding and dopamine uptake by pcp analogs[j]. pharmacology biochemistry and behavior, 1989, 32(3): 699-705.
[3] seeman p. brain dopamine receptors[j]. pharmacological reviews, 1980, 32(3): 229-313.
[4] maurice t, vignon j, kamenka j m, et al. in vivo labelling of the mouse dopamine uptake complex with the phencyclidine derivative [3 h] btcp[j]. neuroscience letters, 1989, 101(2): 234-238.
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