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28395-03-1 分子结构
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3-(butylamino)-4-phenoxy-5-sulfamoylbenzoic acid

ChemBase编号:764
分子式:C17H20N2O5S
平均质量:364.4161
单一同位素质量:364.10929275
SMILES和InChIs

SMILES:
S(=O)(=O)(N)c1c(Oc2ccccc2)c(NCCCC)cc(c1)C(=O)O
Canonical SMILES:
CCCCNc1cc(cc(c1Oc1ccccc1)S(=O)(=O)N)C(=O)O
InChI:
InChI=1S/C17H20N2O5S/c1-2-3-9-19-14-10-12(17(20)21)11-15(25(18,22)23)16(14)24-13-7-5-4-6-8-13/h4-8,10-11,19H,2-3,9H2,1H3,(H,20,21)(H2,18,22,23)
InChIKey:
MAEIEVLCKWDQJH-UHFFFAOYSA-N

引用这个纪录

CBID:764 http://www.chembase.cn/molecule-764.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
3-(butylamino)-4-phenoxy-5-sulfamoylbenzoic acid
IUPAC传统名
bumetanide
商标名
Bumex
Burine
Burinex
Fontego
Fordiuran
Lixil
Lunetoron
Segurex
别名
3-(Aminosulfonyl)-5-(butylamino)-4-phenoxybenzoic acid
Bumetanide
3-(Aminosulfonyl)-5-(butylamino)-4-phenoxy-benzoic Acid
3-(Butylamino)-4-phenoxy-5-sulfamoylbenzoic Acid
Bufenox
Burinex
Fordiuran
Lixil
Lunetoron
PF 1593
3-(butylamino)-4-phenoxy-5-sulfamoylbenzoic acid
Bumetanida [INN-Spanish]
Bumetanidum [INN-Latin]
Bumetanide
Bumex
Ro 10-6338
CAS号
28395-03-1
EC号
249-004-6
MDL号
MFCD00078949
PubChem SID
160964227
24278265
46508147
PubChem CID
2471

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 4.6927853  质子受体
质子供体 LogD (pH = 5.5) 1.6518241 
LogD (pH = 7.4) -0.1262592  Log P 2.4234617 
摩尔折射率 95.7803 cm3 极化性 36.81077 Å3
极化表面积 118.72 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 3.44  LOG S -4.15 
溶解度 2.57e-02 g/l 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
>20 mg/mL (in base) expand 查看数据来源
Acetone expand 查看数据来源
Benzene expand 查看数据来源
Ethanol expand 查看数据来源
Methanol expand 查看数据来源
Propylene Glycol expand 查看数据来源
外观
White Solid expand 查看数据来源
熔点
230-231°C expand 查看数据来源
疏水性(logP)
2.6 expand 查看数据来源
3.372 expand 查看数据来源
保存条件
-20°C expand 查看数据来源
2-8°C expand 查看数据来源
Refrigerator expand 查看数据来源
RTECS编号
DG4910000 expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
纯度
≥98% expand 查看数据来源
95% expand 查看数据来源
97% expand 查看数据来源
99% expand 查看数据来源
成盐信息
Free Base expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals DrugBank DrugBank Selleck Chemicals Selleck Chemicals Sigma Aldrich Sigma Aldrich TRC TRC
MP Biomedicals -  02154263 external link
(Ro 10-6338) White micronized solid Purity: 99% An inhibitor of sodium and potassium cotransport.
DrugBank -  DB00887 external link
Item Information
Drug Groups approved
Description A sulfamyl diuretic. [PubChem]
Indication For the treatment of edema associated with congestive heart failure, hepatic and renal disease including the nephrotic syndrome.
Pharmacology Bumetanide is a loop diuretic of the sulfamyl category to treat heart failure. It is often used in patients in whom high doses of furosemide are ineffective. There is however no reason not to use bumetanide as a first choice drug. The main difference between the two substances is in bioavailability. It is said to be a more predictable diuretic, meaning that the predictable absorption is reflected in a more predictable effect. Bumetanide is 40 times more potent than furosemide (for patients with normal renal function).
Toxicity Overdosage can lead to acute profound water loss, volume and electrolyte depletion, dehydration, reduction of blood volume and circulatory collapse with a possibility of vascular thrombosis and embolism. Electrolyte depletion may be manifested by weakness, dizziness, mental confusion, anorexia, lethargy, vomiting and cramps. Treatment consists of replacement of fluid and electrolyte losses by careful monitoring of the urine and electrolyte output and serum electrolyte levels.
Affected Organisms
Humans and other mammals
Biotransformation 45% is secreted unchanged. Urinary and biliary metabolites are formed by oxidation of the N-butyl side chain.
Absorption Bumetanide is completely absorbed (80%), and the absorption is not altered when taken with food. Bioavailability is almost complete.
Half Life 60-90 minutes
Protein Binding 97%
Elimination Oral administration of carbon-14 labeled Bumex to human volunteers revealed that 81% of the administered radioactivity was excreted in the urine, 45% of it as unchanged drug. Biliary excretion of Bumex amounted to only 2% of the administered dose.
Clearance * 0.2 - 1.1 mL/min/kg [preterm and full-term neonates with respiratory disorders]
* 2.17 mL/min/kg [neonates receiving bumetanide for volume overload]
* 1.8 +/- 0.3 mL/min/kg [geriatric subjects]
* 2.9 +/- 0.2 mL/min/kg [younger subjects]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com
Selleck Chemicals -  S1287 external link
Research Area: Cardiovascular Disease
Biological Activity:
Bumetanide (Bumex) is a loop diuretic of the sulfamyl category to treat heart failure. Bumetanide is 40 times more potent than furosemide (for patients with normal renal function). [1]
Sigma Aldrich -  B3023 external link
Biochem/physiol Actions
Inhibitor of Na+/K+/Cl- cotransporter.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. B3023.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Toronto Research Chemicals -  B689550 external link
Bumetanide is a diuretic.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • http://en.wikipedia.org/wiki/Bumetanide
  • Ward, A., et al.: Drugs, 28, 426 (1984)
  • Gradeen, C.Y, et al.: J. Anal. Toxicol., 14, 123 (1984)
  • Tata, P.N.V., et al.: Anal. Profiles Drug Subs. Excip., 22, 107 (1984)
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专利

专利

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