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Opioids, Nervous system drug

Categories

Analgesics (10)
Drugs acting on the nervous system (10)
Opioid receptor ligands (10)
Psychoactive drugs (10)
Synthetic opioids (7)
Euphoriants (5)
Mu-opioid agonists (5)
Amines (4)
Bases (chemistry) (4)
Antitussives (3)
Cyclic compounds (3)
Drugs acting on the respiratory system (3)
Ketones (3)
Pharmaceuticals (3)
Alcohols (2)
Anesthetics (2)
Kappa agonists (2)
Alkaloids (1)
Alkaloids found in Iboga (1)
Antiarrhythmic agents (1)
Aromatic compounds (1)
Bromoarenes (1)
Cycloalkanes (1)
Cyclopropanes (1)
Delta-opioid agonists (1)
Dissociative drugs (1)
Drugs acting on the cardiovascular system (1)
Drugs acting on the genito-urinary system (1)
Estrogens (1)
Ethers (1)
General anesthetics (1)
Iboga (1)
Opioid antagonists (1)
Phytoestrogens (1)
Piperidines (1)
Sex hormones (1)
Six-membered rings (1)
Sodium channel blockers (1)
Three-membered rings (1)
Xenoestrogens (1)

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Sigma Aldrich (2)

methadone (76-99-3)  
Dolophine  ·  Methadone Hydrochloride  ·  Amidone
Methadone, sold under the brand name Dolophine, among others, is an opioid used to treat pain and as maintenance therapy or to help with tapering in people with opioid dependence. Detoxification using methadone can either be done relatively rapidly in less than a month or gradually over as long as six months. While a single dose has a rapid effect, maximum effect can take five days of use.
ANILERIDINE (144-14-9)  
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.
Levomethadone (125-58-6)  
Levomethadone (INN; L-Polamidon, L-Polamivet, Levadone, Levothyl), or levamethadone, is a synthetic opioid analgesic and antitussive which is marketed in Europe and is used for pain management and in opioid maintenance therapy. In addition to being used as a pharmaceutical drug itself, levomethadone, or R-(−)-methadone, is the active enantiomer of methadone, having approximately 50x the potency of the S-(+)-enantiomer as well as greater μ-opioid receptor selectivity. Accordingly, it is about twice as potent as methadone by weight and its effects are virtually identical in comparison.
S-Methadone (5653-80-5)  
Dextromethadone is an antitussive opioid. It is the (S)-enantiomer of methadone. Dextromethadone acts as a N-methyl-D-aspartate NMDA receptor antagonist similar to ketamine.
EMBUTRAMIDE (15687-14-6)  
N-(2-(3-methoxyphenyl)-2-ethylbutyl-(1))-gamma-hydroxybutyramide
Embutramide (INN, USAN, BAN) (brand name Embutane) is a potent opioid analgesic and sedative drug that is structurally related to methadone. It was developed by Hoechst A.G. in 1958 and was investigated as a general anesthetic agent, but was found to have a very narrow therapeutic window, with a 50 mg/kg dose producing effective sedation and a 75 mg/kg dose being fatal.
Bremazocine (83829-76-9, 75684-07-0, 79665-42-2)  
bremazocine hydrochloride, (2R)-isomer  ·  bremazocine hydrochloride, (+-)-isomer  ·  2-(1-hydroxy-cyclopropylmethyl)-5-ethyl-9,9-dimethyl-2'-hydroxy-6,7-benzomorphan
Bremazocine is a κ-opioid receptor agonist related to pentazocine. It has potent and long-lasting analgesic and diuretic effects. It has 200 times the activity of morphine, but appears to have no addictive properties and does not depress breathing.
CYCLORPHAN (4163-15-9)  
Cyclorphan is an opioid analgesic of the morphinan family that was never marketed. It acts as a μ-opioid receptor (MOR) weak partial agonist or antagonist, κ-opioid receptor (KOR) full agonist, and, to a much lesser extent, δ-opioid receptor (DOR) agonist (75-fold lower affinity relative to the KOR). The drug was first synthesized in 1964 by scientists at Research Corporation.
BROMADOLINE (67579-24-2)  
Bromadoline (U-47931E) is an opioid analgesic selective for the μ-opioid receptor developed by the Upjohn company in the 1970s.The drug has a potency lying between that of codeine and morphine, being slightly stronger than pentazocine. Bromadoline is related to AH-7921 and U-47700.
CORONARIDINE (467-77-6)  
coronardine monohydrochloride  ·  coronardine monohydrochloride, (+-)-isomer  ·  coronardine

Related Results:
buprenorphine (52485-79-7)  
Buprenex  ·  Buprenorphine Hydrochloride  ·  Subutex
Buprenorphine, sold under the brand name Subutex, among others, is an opioid used to treat opioid addiction, acute pain, and chronic pain. It can be used under the tongue, by injection, as a skin patch, or as an implant. When used for opioid addiction it is recommended that a health care provider observe the person while they take the medication.
Subutex (53152-21-9)  
Buprenorphine  ·  Buprenex  ·  Buprenorphine Hydrochloride
oxycodone (76-42-6, 124-90-3)  
Oxycontin  ·  Oxycodone Hydrochloride  ·  Dihydrohydroxycodeinone
Oxycodone is a semisynthetic opioid synthesized from thebaine, an opioid alkaloid found in the Persian poppy, and one of the many alkaloids found in the opium poppy. It is a moderately potent opioid pain medication (orally roughly 1.5 times more potent than morphine), generally indicated for relief of moderate to severe pain. Oxycodone was developed in 1917 in Germany as one of several semi-synthetic opioids in an attempt to improve on the existing opioids.
Oxycodone hydrochloride (124-90-3)  
Oxycodone  ·  Oxycontin  ·  Dihydrohydroxycodeinone
Oxycodone is a semisynthetic opioid synthesized from thebaine, an opioid alkaloid found in the Persian poppy, and one of the many alkaloids found in the opium poppy. It is a moderately potent opioid pain medication (orally roughly 1.5 times more potent than morphine), generally indicated for relief of moderate to severe pain. Oxycodone was developed in 1917 in Germany as one of several semi-synthetic opioids in an attempt to improve on the existing opioids.
Tramadol (123154-38-1, 27203-92-5)  
Ultram  ·  Tramal  ·  Tramadol Hydrochloride
Tramadol, sold under the brand name Ultram among others, is an opioid pain medication used to treat moderate to moderately severe pain. When taken by mouth in an immediate-release formulation, the onset of pain relief usually occurs within an hour. It is often combined with paracetamol (acetaminophen) as this is known to improve the efficacy of tramadol in relieving pain.
Diacetylmorphine (561-27-3)  
Heroin  ·  Diamorphine  ·  Heroin Hydrochloride
Heroin, also known as diamorphine among other names, is an opioid most commonly used as a recreational drug for its euphoric effects. Medically it is used in several countries to relieve pain or in opioid replacement therapy. Heroin is typically injected, usually into a vein; however, it can also be smoked, snorted or inhaled.
Heroin hydrochloride (1502-95-0)  
Heroin  ·  Diamorphine  ·  Diacetylmorphine
Nefopam hydrochloride (69319-31-9, 23327-57-3)  
Ajan  ·  Nefopam  ·  3M Brand of Nefopam Hydrochloride
gabapentin (60142-96-3)  
Neurontin  ·  PMS-Gabapentin  ·  Novo-Gabapentin
Gabapentin, sold under the brand names Neurontin among others, is a medication used to treat epilepsy, neuropathic pain, hot flashes, and restless legs syndrome. In epilepsy, it may be used for those with partial seizures. It is recommended as one of a number of first line medications for the treatment of neuropathic pain in diabetic neuropathy, postherpetic neuralgia, and central neuropathic pain.
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Opioids
Nervous system drug
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