Pukatein je alkaloid koji je prisutan u kori novozelandskog drveta Laurelia novae-zelandiae ("Pukatea"). Ekstrakt kore se koristi kao tradicionalni maorski biljni lek koji deluje kao analgetik.[4][5] Smatra se da je pukatein aktivna komponenta,[6] jer je sličan po strukturi i aktivnosti sa alkaloidima poput glaucina i tetrahidropalmatina koji su prisutni u kineskim medicinskim biljkama sa analgetskom primenom. Pukatein ima višestruke mehanizme dejstva, pri čemu su najprominentnija njegova dejstva kao agonist D2 dopaminskog receptora i antagonist α1 adrenergičkog receptora.[7][8]
Pukatein
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(IUPAC) ime
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(7aR)-7-metil-6,7,7a,8-tetrahidro-5H-benzo[g][1,3]benzodioksolo[6,5,4-de]hinolin-12-ol
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Klinički podaci
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Identifikatori
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CAS broj
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81-67-4
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ATC kod
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nije dodeljen
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PubChem[1][2]
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442340
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ChEMBL[3]
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CHEMBL258370 Y
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Hemijski podaci
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Formula
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C18H17NO3
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Mol. masa
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295,332 g/mol
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SMILES
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eMolekuli & PubHem
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InChI |
InChI=1S/C18H17NO3/c1-19-6-5-11-8-14-18(22-9-21-14)17-15(11)12(19)7-10-3-2-4-13(20)16(10)17/h2-4,8,12,20H,5-7,9H2,1H3/t12-/m1/s1 Y Key: IKMXUUHNYQWZBC-GFCCVEGCSA-N Y |
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Sinonimi
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(R)-11-hydroxy-1,2-methylenedioxyaporphine
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Farmakoinformacioni podaci
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Trudnoća
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?
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Pravni status
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- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
- ↑ Pukatea. Te Ara: The Encyclopedia of New Zealand
- ↑ Pukatea. University of Otago Pharmacy Dept.
- ↑ Fogg WS. The Pharmacological Action of Pukateine. Journal of Pharmacology And Experimental Therapeutics. 1935 Jun;54(2):167-187.
- ↑ Dajas-Bailador FA, Asencio M, Bonilla C, Scorza MC, Echeverry C, Reyes-Parada M, Silveira R, Protais P, Russell G, Cassels BK, Dajas F. Dopaminergic pharmacology and antioxidant properties of pukateine, a natural product lead for the design of agents increasing dopamine neurotransmission. General Pharmacology. 1999 Mar;32(3):373-9. PMID 10211594
- ↑ Valiente M, D'Ocon P, Noguera MA, Cassels BK, Lugnier C, Ivorra MD. Vascular activity of (-)-anonaine, (-)-roemerine and (-)-pukateine, three natural 6a(R)-1,2-methylenedioxyaporphines with different affinities for alpha1-adrenoceptor subtypes. Planta Medica. 2004 Jul;70(7):603-9. PMID 15254852