| Weight | 352.478 g/mol |
|---|---|
| Formula | C22H28N2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
ANILERIDINE (144-14-9)
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- Comparing the effects of anileridine, alphaprodine and fentanyl on schedule-controlled responding by pigeons. (Journal of Pharmacology and Experimental Therapeutics, 1978)
- Studies of analgesic drugs: anileridine dihydrochloride. (Anesthesiology, 1957)
- Comparison of morphine, meperidine, anileridine, and alphaprodine on schedule-controlled responding and analgesia (Pharmacology, Biochemistry and Behavior, 1980)
- Radioimmunoassay for normeperidine: studies on the N-dealkylation of meperidine and anileridine. (Journal of Pharmacology and Experimental Therapeutics, 1977)
- Comparison of anileridine and meperidine as obstetric analgesia: A double blind study of 471 patients (American Journal of Obstetrics and Gynecology, 1966)
- PHARMACOLOGY OF ETHYL-1-(4-AMINOPHENETHYL)-4-PHENYLISONIPECOTATE, ANILERIDINE, A NEW POTENT SYNTHETIC ANALGESIC (Journal of Pharmacology and Experimental Therapeutics, 1957)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCOC(=O)C1(CCN(CC1)CCC2=CC=C(C=C2)N)C3=CC=CC=C3
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InChIKeyLKYQLAWMNBFNJT-UHFFFAOYSA-N
- Pubchem - ANILERIDINE
- Wikipedia - anileridine
Anileridine (trade name: Leritine) is a synthetic analgesic drug and is a member of the piperidine class of analgesic agents developed by Merck & Co. in the 1950s. It differs from pethidine (meperidine) in that the N-methyl group of meperidine is replaced by an N-aminophenethyl group, which increases its analgesic activity.
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