| 词条 | Bunitrolol |
| 释义 |
| ImageFile = Bunitrolol.svg | ImageSize = 200px | ImageAlt = | ImageFile2 = Bunitrolol-3D-balls.png | IUPACName = 2-[3-(tert-Butylamino)-2-hydroxypropoxy]benzonitrile | OtherNames = |Section1={{Chembox Identifiers | CASNo = 34915-68-9 | PubChem = 2473 | ChemSpiderID = 2379 | ChEMBL = 418134 | KEGG = D01444 | UNII = F2613LO055 | InChI = 1/C14H20N2O2/c1-14(2,3)16-9-12(17)10-18-13-7-5-4-6-11(13)8-15/h4-7,12,16-17H,9-10H2,1-3H3 | InChIKey = VCVQSRCYSKKPBA-UHFFFAOYAU | StdInChI = 1S/C14H20N2O2/c1-14(2,3)16-9-12(17)10-18-13-7-5-4-6-11(13)8-15/h4-7,12,16-17H,9-10H2,1-3H3 | StdInChIKey = VCVQSRCYSKKPBA-UHFFFAOYSA-N | SMILES = CC(C)(C)NCC(COC1=CC=CC=C1C#N)O}} |Section2={{Chembox Properties | C=14 | H=20 | N=2 | O=2 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Bunitrolol is a beta-adrenergic antagonist.[1] References1. ^{{cite journal|pmid=20310018|year=2010|last1=Haddad|first1=S|last2=Poulin|first2=P|last3=Funk|first3=C|title=Extrapolating in vitro metabolic interactions to isolated perfused liver: Predictions of metabolic interactions between R-bufuralol, bunitrolol, and debrisoquine|volume=99|issue=10|pages=4406–26|doi=10.1002/jps.22136|journal=Journal of Pharmaceutical Sciences}} {{Adrenergics}}{{cardiovascular-drug-stub}} 2 : Beta blockers|Nitriles |
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