Weight | 273.376 g/mol |
---|---|
Formula | C17H23NO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
TILIDINE
Valerone · Tilidine Hydrochloride, (+-)-211Trans · Tilidine Hydrochloride
51931-66-9, 32447-90-8, 20380-58-9
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- Antagonism between tilidine and naloxone on cerebral potentials and pain ratings in man. (European Journal of Pharmacology, 1983)
- Comparative respiratory depression of tilidine and morphine (Clinical Pharmacology & Therapeutics, 1975)
- Topical Review on the Abuse and Misuse Potential of Tramadol and Tilidine in Germany (Substance Abuse, 2013)
- Pain Relief and Sputum Prostaglandins in Adults Treated with Pethidine, Tilidine and Indomethacin After Tonsillectomy: A DoubleBlind Study (Acta Anaesthesiologica Scandinavica, 1980)
- Pharmacokinetics of tilidine and metabolites in man. (Drug Research, 1989)
- Comparison of tilidine/naloxone, tramadol and bromfenac in experimental pain: a double-blind randomized crossover study in healthy human volunteers. (International Journal of Clinical Pharmacology and Therapeutics, 1999)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Valerone
- Tilidine Hydrochloride, (+-)-211Trans
- Tilidine Hydrochloride
- Tilidate
- Go1261
- Tilidin Godecke
- Go 1261
- Valoron
- Go-1261
- Tilidine Hydrochloride, (+)-Trans
-
SMILESCCOC(=O)C1(CCC=CC1N(C)C)C2=CC=CC=C2
-
InChIKeyWDEFBBTXULIOBB-UHFFFAOYSA-N
- Pubchem - TILIDINE
- Wikipedia - dextilidine
Tilidine, or tilidate (brand names: Tilidin, Valoron and Valtran) is a synthetic opioid painkiller, used mainly in Germany, Switzerland, South Africa and Belgium for treatment of moderate to severe pain, both acute and chronic. Its onset of pain relief after oral administration is about 1015 minutes and peak relief from pain occurs about 2550 minutes after oral administration.
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