Cimaterol

Cimaterol
	(RS)-2-amino-5-[1-hidroksi-2-(izopropilamino)etil]benzonitril
Identifikacija
CAS registarski broj	54239-37-1
PubChem	2755
ChemSpider	2653
KEGG	D03502
MeSH	cimaterol
Jmol-3D slike	Slika 1
SMILES
	CC(C)NCC(C1=CC(=C(C=C1)N)C#N)O
InChI
	InChI=1S/C12H17N3O/c1-8(2)15-7-12(16)9-3-4-11(14)10(5-9)6-13/h3-5,8,12,15-16H,7,14H2,1-2H3 ; Kod: BUXRLJCGHZZYNE-UHFFFAOYSA-N InChI=1/C12H17N3O/c1-8(2)15-7-12(16)9-3-4-11(14)10(5-9)6-13/h3-5,8,12,15-16H,7,14H2,1-2H3; Kod: BUXRLJCGHZZYNE-UHFFFAOYAC
Svojstva
Molekulska formula	C12H17N3O
Molarna masa	219,28288
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Cimaterol je beta-adrenergički agonist.^[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.
↑ Byrem TM, Beermann DH, Robinson TF (April 1998). „The beta-agonist cimaterol directly enhances chronic protein accretion in skeletal muscle”. J. Anim. Sci. 76 (4): 988–98. PMID 9581921. ^{[mrtav link]}

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