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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/08/27 01:03:29」(JST)

Indenolol is a beta-adrenergic blocker.^[1]

References

^ Ali, I; Gaitonde, VD; Aboul-Enein, HY; Hussain, A (2009). "Chiral separation of beta-adrenergic blockers on CelluCoat column by HPLC". Talanta. 78 (2): 458–63. doi:10.1016/j.talanta.2008.11.043. PMID 19203609.

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Enantio-separation of drugs with multiple chiral centers by chromatography and capillary electrophoresis.

Al-Othman ZA1, Al-Warthan A, Alam SD, Ali I.
Biomedical chromatography : BMC.Biomed Chromatogr.2014 Nov;28(11):1514-24. doi: 10.1002/bmc.3259. Epub 2014 Jul 28.
Some drugs with more than one chiral center are of high medicinal values. However, the chiral resolution of such types of racemate is a challenging task for scientists. The evolution of efficient chiral selectors is a hope for the future. Some papers have described such types of chiral resolution. T
PMID 25067822

The pH sensitivity of -NH exchange in LnDOTA-tetraamide complexes varies with amide substituent.

Opina AC1, Wu Y, Zhao P, Kiefer G, Sherry AD.
Contrast media & molecular imaging.Contrast Media Mol Imaging.2011 Nov-Dec;6(6):459-64. doi: 10.1002/cmmi.445.
The amide proton exchange rates in various lanthanide(III) DOTA-tetraamide complexes were investigated by CEST as a function of variable chemical structures and charges on the amide substituents. Comparisons were made between YbDOTA-(gly)(4)(-) (Yb-1), YbDOTA-(NHCH(2)PO(3))(4 (5-) (Yb-2) and YbDOTA-
PMID 22144023

Chiral separations of some beta-adrenergic agonists and antagonists on AmyCoat column by HPLC.

Ali I1, Saleem K, Gaitonde VD, Aboul-Enein HY, Hussain I.
Chirality.Chirality.2010 Jan;22(1):24-8. doi: 10.1002/chir.20697.
Sixteen beta-adrenergic antagonists namely acebutalol, alprenolol, atenolol, bisoprolol, bopindolol, bufurolol, carazolol, celiprolol, indenolol, metaprolol, nebivolol, oxprenolol, practolol, propranolol, tertalol, and timolol, and two beta-adrenergic agonists namely cimeterol and clenbuterol were r
PMID 19208401

小池一喜,吉川圭一郎,原和彦,篠崎貴弘,深津康仁,岡地サユミ,柴田典明,長谷川和哉,大澤一郎,松浦信人,後藤實,工藤逸郎
日本歯科心身医学会雑誌 12(2), 169-174, 1997
… It is known that the anxiety and sympathetically-medicated hypertension induced by dental procedures can be lessened by the hearing of music.<BR>In the present study, we measured the physiological effects of music-listening, especially on digital prethysm.ography (PTG) and the heat rate (HR), and compared them with the effects induced by the administration of indenolol hydrochloride, a β-blocker for pharmacological anti-stress treatment. … indenolol hydrochloride prior to the stress-inducing treatment. …
NAID 130004307913

小池一喜,渡辺幹夫,石川精一,宮田幸忠,原邦嘉,後藤實,押尾英一,工藤逸郎
日本歯科心身医学会雑誌 9(1), 75-79, 1994
… Group 2: 8 subjects pre-treated with 10mg of a beta-blocker indenolol hydrochloride. … Group 2 was orally administered of 10mg indenolol hydrochloride, a first generation betablocker, one hour before injection into the oral cavity. …
NAID 130004105575

β-アドレナリン受容体遮断薬のβ-遮断作用,局所麻酔作用,膜安定化作用の効力の比較,並びに,Strophanthin-Gのモルモット心毒性発現に対する影響に関する研究

杉本治良,湯浅精一,鈴木雅泰
関西医科大学雑誌 39(4), 418-429, 1987
… The influence of alprenolol, carteolol, indenolol, pindolol, practolol, and propranolol on the effect of isoproterenol in isolated guinea-pig atrial contraction rate was examined comparing their beta-blocking actions, and their influence on the responses of guinea-pig cornea and dorsal skin to the mechanical stimulation was tested comparing their local anaesthetic actions. …
NAID 130004701322

リンク元	「インデノロール」
拡張検索	「indenolol hydrochloride」

Indenolol
Names
	IUPAC name 1-(1H-Inden-4-yloxy)-3-(propan-2-ylamino)propan-2-ol
Identifiers
CAS Number	60607-68-3
ChEMBL	ChEMBL153585
ChemSpider	64962
DrugBank	DB08952
EC Number	262-323-5
Jmol 3D model	Interactive image
KEGG	D08078
PubChem	71955
	InChI InChI=1S/C15H21NO2/c1-11(2)16-9-13(17)10-18-15-8-4-6-12-5-3-7-14(12)15/h3-4,6-8,11,13,16-17H,5,9-10H2,1-2H3 Key: MPGBPFMOOXKQRX-UHFFFAOYSA-N ; InChI=1/C15H21NO2/c1-11(2)16-9-13(17)10-18-15-8-4-6-12-5-3-7-14(12)15/h3-4,6-8,11,13,16-17H,5,9-10H2,1-2H3 Key: MPGBPFMOOXKQRX-UHFFFAOYAY ;
	SMILES CC(C)NCC(COC1=CC=CC2=C1C=CC2)O ;
Properties
Chemical formula	C15H21NO2
Molar mass	247.34 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references