Kloranolol

Kloranolol
	(RS)-1-(tert-butilamino)-3-(2,5-dihlorofenoksi)propan-2-ol
Identifikacija
CAS registarski broj	39563-28-5
PubChem	65814
ChemSpider	59229
KEGG	D07183
ATC code	C07AA27
Jmol-3D slike	Slika 1
SMILES
	Clc1ccc(Cl)cc1OCC(O)CNC(C)(C)C
InChI
	InChI=1S/C13H19Cl2NO2/c1-13(2,3)16-7-10(17)8-18-12-6-9(14)4-5-11(12)15/h4-6,10,16-17H,7-8H2,1-3H3 ; Kod: XYCMOTOFHFTUIU-UHFFFAOYSA-N InChI=1/C13H19Cl2NO2/c1-13(2,3)16-7-10(17)8-18-12-6-9(14)4-5-11(12)15/h4-6,10,16-17H,7-8H2,1-3H3; Kod: XYCMOTOFHFTUIU-UHFFFAOYAX
Svojstva
Molekulska formula	C13H19Cl2NO2
Molarna masa	292,20146
	; ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Kloranolol (tobanum) je beta blokator.^[5]

Reference

↑ 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.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
↑ Kulcsár-Gergely J. (1989). Action of beta-adrenoceptor blockers on liver function of rats. 39. pp. 782-5.

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