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Bufuralol

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names：
1-(7-Ethylbenzofuran-2-yl)-2-tert-butylamino-1-hydroxyethane
CAS號：
54340-62-4
MDL Number：
MF(分子式)： C16H23NO2 MW(分子量)： 261.37
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文別名	Bufuralol
英文別名	Bufuralol; Ro 3-4787; Ro-3-4787; Ro3-4787
CAS號	54340-62-4
Inchi	InChI=1S/C16H23NO2/c1-5-11-7-6-8-12-9-14(19-15(11)12)13(18)10-17-16(2,3)4/h6-9,13,17-18H,5,10H2,1-4H3
InchiKey	SSEBTPPFLLCUMN-UHFFFAOYSA-N
分子式 Formula	C16H23NO2
分子量 Molecular Weight	261.37
溶解度Solubility
性狀	Solid powder
儲藏條件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

產品說明	Bufuralol(CAS:54340-62-4):僅限應用于工業(yè)或者科學研究過程中非醫(yī)療目的，不應用于人類或動物的臨床診斷以及治過程療，該產品非藥用，非食用。
Introduction	Bufuralol is a Adrenergic Agent.
Application1
Application2
Application3

警示圖
危險性	Warning
危險性警示
安全聲明
安全防護
備注

[1]Uehara S, Uno Y, Hagihira Y, Murayama N, Shimizu M, Inoue T, Sasaki E, Yamazaki H. Marmoset cytochrome P450 2D8 in livers and small intestines metabolizes typical human P450 2D6 substrates, metoprolol, bufuralol and dextromethorphan. Xenobiotica. 2015;45(9):766-72. doi: 10.3109/00498254.2015.1019595. Epub 2015 Jul 27. PubMed PMID: 25801057.

[2]Cai J, Dai DP, Geng PW, Wang SH, Wang H, Zhan YY, Huang XX, Hu GX, Cai JP. Effects of 22 Novel CYP2D6 Variants Found in the Chinese Population on the Bufuralol and Dextromethorphan Metabolisms In Vitro. Basic Clin Pharmacol Toxicol. 2016 Mar;118(3):190-9. doi: 10.1111/bcpt.12478. Epub 2015 Sep 26. PubMed PMID: 26310775.

[3] Pringle TH, Francis RJ, East PB, Shanks RG. Pharmacodynamic and pharmacokinetic studies on bufuralol in man. Br J Clin Pharmacol. 1986 Nov;22(5):527-34. PubMed PMID: 2878678; PubMed Central PMCID: PMC1401192.

[4] Johnston GD, Finch MB, Shanks RG. Peripheral vascular effects of bufuralol in hypertensive and normal subjects: a comparison with propranolol and pindolol. Eur J Clin Pharmacol. 1986;30(6):649-52. PubMed PMID: 3533562.

[5] Mankowski DC. The role of CYP2C19 in the metabolism of (+/-) bufuralol, the prototypic substrate of CYP2D6. Drug Metab Dispos. 1999 Sep;27(9):1024-8. PubMed PMID: 10460802.

6: Balant L, Francis RJ, Tozer TN, Marmy A, Tschopp JM, Fabre J. Influence of renal failure on the hepatic clearance of bufuralol in man. J Pharmacokinet Biopharm. 1980 Oct;8(5):421-38. PubMed PMID: 6114166.7: Yamazaki H, Guo Z, Persmark M, Mimura M, Inoue K, Guengerich FP, Shimada T. Bufuralol hydroxylation by cytochrome P450 2D6 and 1A2 enzymes in human liver microsomes. Mol Pharmacol. 1994 Sep;46(3):568-77. PubMed PMID: 7935340.8: Foti RS, Fisher MB. Impact of incubation conditions on bufuralol human clearance predictions: enzyme lability and nonspecific binding. Drug Metab Dispos. 2004 Mar;32(3):295-304. PubMed PMID: 14977863.9: Shimada T, Tsumura F, Yamazaki H, Guengerich FP, Inoue K. Characterization of (+/-)-bufuralol hydroxylation activities in liver microsomes of Japanese and Caucasian subjects genotyped for CYP2D6. Pharmacogenetics. 2001 Mar;11(2):143-56. PubMed PMID: 11266079.10: Meyer UA, Gut J, Kronbach T, Skoda C, Meier UT, Catin T, Dayer P. The molecular mechanisms of two common polymorphisms of drug oxidation--evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation. Xenobiotica. 1986 May;16(5):449-64. PubMed PMID: 2874666.1

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