This is a list of opioids, opioid antagonists and inverse agonists.

Opium poppy (Papaver somniferum) flower

Opium and poppy straw derivatives edit

 
Seedhead of opium poppy with white latex

Crude opiate extracts whole opium products edit

Natural opiates edit

Opium alkaloids edit

Structures

Alkaloid salts mixtures edit

Semisynthetics including Bentley compounds edit

Morphine family edit

3,6-diesters of morphine edit

Structures

Codeine-dionine family edit

Morphinones and morphols edit

Morphides edit

Dihydrocodeine series edit

Nitrogen morphine derivatives edit

Hydrazones edit

Structures
Hydrazones
  Oxymorphazone

Halogenated morphine derivatives edit

Structures

Active opiate metabolites edit

Morphinans edit

 
Levomethorphan

Morphinan series edit

Others edit

Benzomorphans edit

4-Phenylpiperidines edit

 
Pethidine

Pethidines (meperidines) edit

Prodines edit

Ketobemidones edit

Others edit

Structures
Other phenylpiperidines
 Alvimopan   Loperamide   LS-115509   Picenadol

Open chain opioids edit

 
Methadone

Amidones edit

Methadols edit

Moramides edit

Thiambutenes edit

Phenalkoxams edit

Ampromides edit

Structures

Others edit

Structures
Other open chain opioids
 

Embutramide

 

IC-26

 

Isoaminile

 

Lefetamine

 

R-4066

Anilidopiperidines edit

 
Fentanyl

Oripavine derivatives edit

 
Thienorphine

Phenazepanes edit

Pirinitramides edit

Structures
Pirinitramides
 

Bezitramide

 

Piritramide

Benzimidazoles edit

Indoles edit

Beta-Amino Ketones edit

Diphenylmethylpiperazines edit

Structures
Diphenylmethylpiperazines
 

BW373U86

 

DPI-221

 

DPI-287

 

DPI-3290

 

SNC-80

Opioid peptides edit

 
β-neoendorphin

Dynorphins edit

Structures

Endomorphins edit

Endorphins edit

Enkephalins edit

Propeptides edit

Others / unknown edit

Others edit

Opioid antagonists and inverse agonists edit

Biased ligands edit

Receptor heteromer targeting ligands edit

Uncategorized opioids edit

Combination drug formulations containing opioids edit

See also edit

References edit

  1. ^ ChemIndex CAS Registry Number 3371-56-0
  2. ^ ChemIndex CAS Registry Number 509-56-8
  3. ^ ChemIndex CAS Registry Number 63715-94-6
  4. ^ NCBI PubChem SID 750205
  5. ^ chembase [permanent dead link] cbid_346222
  6. ^ Gomes I, Fujita W, Gupta A, Saldanha SA, Saldanha AS, Negri A, Pinello CE, Eberhart C, Roberts E, Filizola M, Hodder P, Devi LA (2013). "Identification of a μ-δ opioid receptor heteromer-biased agonist with antinociceptive activity". Proc. Natl. Acad. Sci. U.S.A. 110 (29): 12072–7. Bibcode:2013PNAS..11012072G. doi:10.1073/pnas.1222044110. PMC 3718106. PMID 23818586.
  7. ^ Yekkirala AS, Lunzer MM, McCurdy CR, Powers MD, Kalyuzhny AE, Roerig SC, Portoghese PS (2011). "N-naphthoyl-beta-naltrexamine (NNTA), a highly selective and potent activator of μ/kappa-opioid heteromers". Proc. Natl. Acad. Sci. U.S.A. 108 (12): 5098–103. Bibcode:2011PNAS..108.5098Y. doi:10.1073/pnas.1016277108. PMC 3064379. PMID 21385944.

External links edit

  • Carbonate derivatives of 14β-hydroxycodeine "viz., 14β-hydroxy-6-O-(methoxycarbonyl)codeine, 6-O-methoxycarbonyl-14β-(methoxycarbonyloxy)codeine, and 14β-acetoxy-6-O-methoxy-carbonylcodeine, potential substrates for ring C modification in morphinane (sic) alkaloids, were synthesized for the first time." Russian Chemical Bulletin. August 2008, Volume 57, Issue 8, pp 1773–1774. Date: 11 Aug 2009; I. V. Evsikova, S. K. Moiseev, P. V. Petrovskii, V. N. Kalinin. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1739–1740