Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Epiboxidine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Epiboxidine
Legal status
Legal status
  • Investigational
Identifiers
  • (1R,4S,6S)-6-(3-Methylisoxazol-5-yl)-7-azabicyclo[2.2.1]heptane
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC10H14N2O
Molar mass178.235 g·mol−1
3D model (JSmol)
  • CC1=NOC(=C1)[C@H]2C[C@@H]3CC[C@H]2N3
  • InChI=1S/C10H14N2O/c1-6-4-10(13-12-6)8-5-7-2-3-9(8)11-7/h4,7-9,11H,2-3,5H2,1H3/t7-,8-,9+/m0/s1
  • Key:GEEFPQBPVBFCSD-XHNCKOQMSA-N

Epiboxidine is a chemical compound which acts as apartial agonist at neuralnicotinic acetylcholine receptors, binding to both theα3β4 and theα4β2subtypes. It was developed as a less toxicanalogue of the potent frog-derivedalkaloidepibatidine, which is around 200 times stronger thanmorphine as ananalgesic but is deadly toxic.

Epiboxidine is around one-tenth as potent as epibatidine as an α4β2 agonist, but has around the same potency as an α3β4 agonist. It has only one-tenth of the analgesic power of epibatidine, but is also much less toxic.[1][2][3]

Uses

[edit]

Despite reduced toxicity compared to epibatidine, epiboxidine itself is still too toxic to be developed as a drug for use in humans. It is used in scientific research[4] and as a parent compound to derive newer analogues which may be safer and have greater potential for clinical development.[5][6][7]

See also

[edit]

References

[edit]
  1. ^Rizzi L, Dallanoce C, Matera C, Magrone P, Pucci L, Gotti C, et al. (August 2008)."Epiboxidine and novel-related analogues: a convenient synthetic approach and estimation of their affinity at neuronal nicotinic acetylcholine receptor subtypes"(PDF).Bioorganic & Medicinal Chemistry Letters.18 (16):4651–4.doi:10.1016/j.bmcl.2008.07.016.hdl:2434/59291.PMID 18644719.
  2. ^Dallanoce C, Matera C, De Amici M, Rizzi L, Pucci L, Gotti C, et al. (July 2012). "The enantiomers of epiboxidine and of two related analogs: synthesis and estimation of their binding affinity at α4β2 and α7 neuronal nicotinic acetylcholine receptors".Chirality.24 (7):543–51.doi:10.1002/chir.22052.PMID 22566097.
  3. ^Badio B, Garraffo HM, Plummer CV, Padgett WL, Daly JW (February 1997)."Synthesis and nicotinic activity of epiboxidine: an isoxazole analogue of epibatidine".European Journal of Pharmacology.321 (2):189–94.doi:10.1016/S0014-2999(96)00939-9.PMID 9063687.
  4. ^Yan X, Zhao B, Butt CM, Debski EA (December 2006). "Nicotine exposure refines visual map topography through an NMDA receptor-mediated pathway".The European Journal of Neuroscience.24 (11):3026–42.doi:10.1111/j.1460-9568.2006.05204.x.PMID 17156364.S2CID 25993659.
  5. ^Fitch RW, Pei XF, Kaneko Y,Gupta T, Shi D, Federova I, Daly JW (January 2004). "Homoepiboxidines: further potent agonists for nicotinic receptors".Bioorganic & Medicinal Chemistry.12 (1):179–90.doi:10.1016/j.bmc.2003.10.015.PMID 14697783.
  6. ^Cheng J, Izenwasser S, Zhang C, Zhang S, Wade D, Trudell ML (April 2004). "Synthesis and nicotinic acetylcholine receptor binding affinities of 2- and 3-isoxazolyl-8-azabicyclo[3.2.1]octanes".Bioorganic & Medicinal Chemistry Letters.14 (7):1775–8.doi:10.1016/j.bmcl.2004.01.025.PMID 15026069.
  7. ^Armstrong A, Bhonoah Y, Shanahan SE (October 2007). "Aza-Prins-pinacol approach to 7-azabicyclo[2.2.1]heptanes: syntheses of (+/-)-epibatidine and (+/-)-epiboxidine".The Journal of Organic Chemistry.72 (21):8019–24.doi:10.1021/jo701536a.PMID 17867705.
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Phenethylpyrrolidines
Racetams
Psychedelics
Tropanes
Tryptamines
Others
Opioids
Opiates/opium
Semisynthetic
Synthetic
Paracetamol-type
NSAIDs
Propionates
Oxicams
Acetates
COX-2 inhibitors
Fenamates
Salicylates
Pyrazolones
Others
Cannabinoids
Ion channel
modulators
Calcium blockers
Sodium blockers
Potassium openers
Myorelaxants
Others
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)
Retrieved from "https://en.wikipedia.org/w/index.php?title=Epiboxidine&oldid=1286908174"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp