| Weight | 261.365 g/mol |
|---|---|
| Formula | C16H23NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
ETHOHEPTAZINE (77-15-6)
ethoheptazine citrate (1:1) · ethoheptazine HCl · ethylheptazine
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- METHODS IN EVALUATING ETHOHEPTAZINE AND ETHOHEPTAZINE COMBINED WITH ASPIRIN (JAMA, 1958)
- Effects of propoxyphene, ethoheptazine, and azabicyclane on schedule-controlled responding: Attenuation by pentobarbital but not naloxone (Psychopharmacology, 1979)
- Mefenamic acid, chlormezanone-paracetamol, ethoheptazine-aspirin-meprobamate: a comparative study in acute low back pain. (The British journal of clinical practice, 1987)
- EthoheptazineMonoamine Oxidase Inhibitor Interaction in Rabbits (Canadian Journal of Physiology and Pharmacology, 1972)
- Analgesic effectiveness of orally administered ethoheptazine in man. (The American Journal of the Medical Sciences, 1957)
- A double-blind comparison of ethoheptazine citrate, propoxyphene hydrochloride, and placebo. (Current Therapeutic Research-clinical and Experimental, 1973)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ethoheptazine citrate (1:1)
- ethoheptazine HCl
- ethylheptazine
- heptacyclazin
-
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-
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- Pubchem - ETHOHEPTAZINE
- Wikipedia - ethoheptazine
Ethoheptazine (trade name Zactane) is an opioid analgesic from the phenazepane family. It was invented in the 1950s and is related to other drugs such as proheptazine and pethidine. Ethoheptazine produces similar effects to other opioids, including analgesia, sedation, dizziness and nausea.
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