Tretoquinol

Tretoquinol
Names
	Preferred IUPAC name (1S)-1-[(3,4,5-Trimethoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol
Identifiers
CAS Number	30418-38-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL174984 ;
ChemSpider	59192 ;
MeSH	Tretoquinol
PubChem CID	65772;
UNII	JIO3275WGI ;
CompTox Dashboard (EPA)	DTXSID7023695 ;
	InChI InChI=1S/C19H23NO5/c1-23-17-7-11(8-18(24-2)19(17)25-3)6-14-13-10-16(22)15(21)9-12(13)4-5-20-14/h7-10,14,20-22H,4-6H2,1-3H3/t14-/m0/s1 Key: RGVPOXRFEPSFGH-AWEZNQCLSA-N ; InChI=1/C19H23NO5/c1-23-17-7-11(8-18(24-2)19(17)25-3)6-14-13-10-16(22)15(21)9-12(13)4-5-20-14/h7-10,14,20-22H,4-6H2,1-3H3/t14-/m0/s1 Key: RGVPOXRFEPSFGH-AWEZNQCLBM;
	SMILES O(c1cc(cc(OC)c1OC)C[C@H]3c2c(cc(O)c(O)c2)CCN3)C;
Properties
Chemical formula	C19H23NO5
Molar mass	345.39 g/mol
Pharmacology
ATC code	R03AC09 (WHO)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

Tretoquinol is a beta-adrenergic agonist.^[1]^[2]

References

^ 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.
^ 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.

This drug article relating to the respiratory system is a stub. You can help Wikipedia by expanding it.

[1] 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.

[2] 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.

[1]

[2]