Tretoquinol is a beta-adrenergic agonist.[1][2]
Names | |
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Preferred IUPAC name
(1S)-1-[(3,4,5-Trimethoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
MeSH | Tretoquinol |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C19H23NO5 | |
Molar mass | 345.39 g/mol |
Pharmacology | |
R03AC09 (WHO) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ Yamato, E.; Hirakura, M.; Sugasawa, S. (1966). "Synthesis of 6,7-dihydrox-1,2,3,4-tetrahydroisoquinoline derivatives". Tetrahedron. 22: 129–134. doi:10.1016/S0040-4020(01)82177-3.129-134&rft.date=1966&rft_id=info:doi/10.1016/S0040-4020(01)82177-3&rft.aulast=Yamato&rft.aufirst=E.&rft.au=Hirakura, M.&rft.au=Sugasawa, S.&rfr_id=info:sid/en.wikipedia.org:Tretoquinol" class="Z3988">
- ^ Konkar, A. A.; Vansal, S. S.; Shams, G.; Fraundorfer, P. F.; Zheng, W. P.; Nikulin, V. I.; De Los Angeles, J.; Fertel, R. H.; Miller, D. D.; Feller, D. R. (1999-11-01). "β-Adrenoceptor Subtype Activities of Trimetoquinol Derivatives: Biochemical Studies on Human β-Adrenoceptors Expressed in Chinese Hamster Ovary Cells". The Journal of Pharmacology and Experimental Therapeutics. 291 (2). Jpet.aspetjournals.org: 875–883. PMID 10525112. Retrieved 2012-08-20.875-883&rft.date=1999-11-01&rft_id=info:pmid/10525112&rft.aulast=Konkar&rft.aufirst=A. A.&rft.au=Vansal, S. S.&rft.au=Shams, G.&rft.au=Fraundorfer, P. F.&rft.au=Zheng, W. P.&rft.au=Nikulin, V. I.&rft.au=De Los Angeles, J.&rft.au=Fertel, R. H.&rft.au=Miller, D. D.&rft.au=Feller, D. R.&rft_id=http://jpet.aspetjournals.org/content/291/2/875.full&rfr_id=info:sid/en.wikipedia.org:Tretoquinol" class="Z3988">