Weight | 283.799 g/mol |
---|---|
Formula | C15H22ClNO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
Pethidine hydrochloride (50-13-5)
Meperidine · Demerol · Dolin
Score:
#33 in Neurology
,
#174 in Neuroscience
,
#847 in Biology
,
#936 in Chemistry
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- Sigma-Aldrich - Pethidine hydrochloride200.00 - 448.35 USD
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- Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis (Science, 1983)
- The formalin test: a quantitative study of the analgesic effects of morphine, meperidine, and brain stem stimulation in rats and cats. (Pain, 1977)
- Chronic parkinsonism secondary to intravenous injection of meperidine analogues (Psychiatry Research-neuroimaging, 1979)
- THE EVALUATION OF THE ANALGESIC ACTION OF PETHIDINE HYDROCHLORIDE (DEMEROL) (Journal of Pharmacology and Experimental Therapeutics, 1944)
- Central nervous system excitatory effects of meperidine in cancer patients (Annals of Neurology, 1983)
- THE EFFECTS OF MORPHINE, METHADONE AND MEPERIDINE ON SOME REFLEX RESPONSES OF SPINAL ANIMALS TO NOCICEPTIVE STIMULATION (Journal of Pharmacology and Experimental Therapeutics, 1951)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Meperidine
- Demerol
- Dolin
- Pethidine
- Meperidine Hydrochloride
- Dolantin
- Dolosal
- Dolargan
- Lydol
- Operidine EPJ-I
- Operidine EPJ I
- Dolsin
- Dolcontral
- Lidol
- Isonipecain
-
SMILESCCOC(=O)C1(CCN(CC1)C)C2=CC=CC=C2.Cl
-
InChIKeyWCNLCIJMFAJCPX-UHFFFAOYSA-N
- Pubchem - Pethidine hydrochloride
- Wikipedia - meperidine hydrochloride
Pethidine, also known as meperidine and sold under the brand name Demerol among others, is a synthetic opioid pain medication of the phenylpiperidine class. Synthesized in 1939 as a potential anticholinergic agent by the German chemist Otto Eisleb, its analgesic properties were first recognized by Otto Schaumann while working for IG Farben, Germany. Pethidine is the prototype of a large family of analgesics including the pethidine 4-phenylpiperidines (piminodine, anileridine and others), the prodines (alphaprodine, MPPP, etc.), bemidones (ketobemidone, etc.) and others more distant, including diphenoxylate and analogues.
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
Similar Compounds
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