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- 2-Aminoindane
- 2-Aminotetralin
- 2-Benzylpiperidine
- 2-Fluoroamphetamine
- 2-MDP
- 2C-B-BZP
- 3-CPMT
- 3-Fluoroamphetamine
- 3-Methoxyamphetamine
- 3-Methylamphetamine
- 4'-Fluorococaine
- 4-Benzylpiperidine
- 4-Bromomethcathinone
- 4-Ethylamphetamine
- 4-Fluoroamphetamine
- 4-Methylaminorex
- 4-Methylamphetamine
- 5-IAI
- 6-Br-APB
- 77-LH-28-1
- 8-Chlorotheophylline
- 8-Phenyltheophylline
- A-349,821
- A-366,833
- A-582,941
- A-77636
- A-84,543
- A-867,744
- ABT-202
- ABT-239
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- ABT-560
- ABT-894
- AC-260,584
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- GABA A receptor
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- GSK-189,254
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- H1 antagonist
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- Heptaminol
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- J-104,129
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- JZ-IV-10
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- Ketamine
- Kynurenic acid
- L-655,708
- L-689,660
- L-DOPA
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- LY-2,033,298
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- LY-503,430
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- Modafinil
- Molecular mass
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- Morazone
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- PBID
- PD-0298029
- PD-102,807
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- PEPA (drug)
- PHA-543,613
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- Pharmaceutical drug
- Phenatine
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- Phosphatidylcholine
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- RTI-150
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- RTI-177
- RTI-183
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- RTI-354
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- RU-47,213
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- S-17092
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- SCH-217,443
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- Scopolamine
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- Synaptic vesicle
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- Tacrine
- Talsaclidine
- Taltirelin
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- TB-21007
- TC-1698
- TC-1734
- TC-1827
- TC-2216
- TC-5214
- TC-5619
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- Tebanicline
- Telenzepine
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- Teniloxazine
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- Tesofensine
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- Thiocolchicoside
- Thiopilocarpine
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- Tolterodine
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- Tranylcypromine
- Trazium
- Tribufos
- Trichlorfon
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- Triethylcholine
- Trihexyphenidyl
- Trimipramine
- Tripelennamine
- Tripitamine
- Triprolidine
- Tropane
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- Tropatepine
- Tropeinium
- Tropicamide
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- Tuaminoheptane
- Tubocurarine
- Tyramine
- Tyrosine
- UB-165
- UH-232
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- Vanoxerine
- Varenicline
- VE (nerve agent)
- Vecuronium
- Vedaclidine
- Vesamicol
- VG (nerve agent)
- Vinpocetine
- VM (nerve agent)
- VR (nerve agent)
- VU-0029767
- VU-0090157
- VU-0152099
- VU-0152100
- VU-0238429
- VX (nerve agent)
- WAY-132,983
- WAY-317,538
- Wikipedia Stub
- WIN 35428
- WIN-2299
- Xamoterol
- Xanomeline
- Xanthine
- Xenon
- XY-4083
- Xylopropamine
- YM-796
- Yohimbine
- Zamifenacin
- Zanapezil
- ZK-93426
- Zylofuramine
- Α-bungarotoxin
- Α-conotoxin
- Α5IA
Cyprodenate (Actebral) is a stimulant drug. It was used for counteracting the effects of benzodiazepine tranquillizer drugs before the development of newer antidotes such as flumazenil. It produces dimethylethanolamine as a metabolite, and so might be expected to produce nootropic effects.
This page contains text from Wikipedia, the Free Encyclopedia -
http://en.wikipedia.org/wiki/Cyprodenate
This article is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License, which means that you can copy and modify it as long as the entire work (including additions) remains under this license.
This article is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License, which means that you can copy and modify it as long as the entire work (including additions) remains under this license.
