Weight | 311.381 g/mol |
---|---|
Formula | C19H21NO3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Nalorphine (62-67-9)
Allylnormorphine · Nalorphine Hydrochloride · Lethidrone
Score:
#2040 in Biology
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#2493 in Chemistry
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- The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog. (Journal of Pharmacology and Experimental Therapeutics, 1976)
- BIOCHEMICAL AND PHARMACOLOGICAL CHANGES IN THE RAT FOLLOWING CHRONIC ADMINISTRATION OF MORPHINE, NALORPHINE AND NORMORPHINE (Journal of Pharmacology and Experimental Therapeutics, 1959)
- The effects of morphine and nalorphine-like drugs in the nondependent, morphine-dependent and cyclazocine-dependent chronic spinal dog. (Journal of Pharmacology and Experimental Therapeutics, 1976)
- Pharmacologic dissociation of behavior and EEG "sleep patterns" in dogs; morphine, n-allylnormorphine, and atropine. (Experimental Biology and Medicine, 1952)
- The analgesic effectiveness of nalorphine and nalorphine-morphine combinations in man. (Journal of Pharmacology and Experimental Therapeutics, 1954)
- N-ALLYLNORMORPHINE: EFFECTS OF SINGLE DOSES AND PRECIPITATION OF ACUTE "ABSTINENCE SYNDROMES" DURING ADDICTION TO MORPHINE, METHADONE OR HEROIN IN MAN (POST-ADDICTS) (Journal of Pharmacology and Experimental Therapeutics, 1953)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Allylnormorphine
- Nalorphine Hydrochloride
- Lethidrone
- Nalorphine Hydrobromide
- Nalorphine, L-tartrate (1:1)
- Nalorphine, (14 alpha)-Isomer
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SMILESC=CCN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O
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InChIKeyUIQMVEYFGZJHCZ-UHFFFAOYSA-N
- Pubchem - Nalorphine
- Wikipedia - nalorphine
Nalorphine (INN) (brand names Lethidrone, Nalline), also known as N-allylnormorphine, is a mixed opioid agonistantagonist with opioid antagonist and analgesic properties. It was introduced in 1954 and was used as an antidote to reverse opioid overdose and in a challenge test to determine opioid dependence. It acts at two opioid receptors the -opioid receptor (MOR) where it has antagonistic effects, and at the -opioid receptor (KOR) (Ki = 1.6 nM; EC50 = 483 nM; Emax = 95%) where it exerts high-efficacy partial agonist/near-full agonist characteristics.
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