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17560-51-9 分子结构
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7-chloro-2-methyl-3-(2-methylphenyl)-4-oxo-1,2,3,4-tetrahydroquinazoline-6-sulfonamide

ChemBase编号:406
分子式:C16H16ClN3O3S
平均质量:365.83454
单一同位素质量:365.06009007
SMILES和InChIs

SMILES:
Clc1cc2NC(N(C(=O)c2cc1S(=O)(=O)N)c1c(cccc1)C)C
Canonical SMILES:
CC1Nc2cc(Cl)c(cc2C(=O)N1c1ccccc1C)S(=O)(=O)N
InChI:
InChI=1S/C16H16ClN3O3S/c1-9-5-3-4-6-14(9)20-10(2)19-13-8-12(17)15(24(18,22)23)7-11(13)16(20)21/h3-8,10,19H,1-2H3,(H2,18,22,23)
InChIKey:
AQCHWTWZEMGIFD-UHFFFAOYSA-N

引用这个纪录

CBID:406 http://www.chembase.cn/molecule-406.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
7-chloro-2-methyl-3-(2-methylphenyl)-4-oxo-1,2,3,4-tetrahydroquinazoline-6-sulfonamide
IUPAC传统名
metolazone (product)
metolazone
商标名
Diulo
Metalazone
Metalozone
Metenix
Microx
Mykrox
Oldren
Xuret
Zaroxolyn
别名
Metolazona [INN-Spanish]
Metolazonum [INN-Latin]
Metolazone
Metolazone
7-Chloro-1,2,3,4-tetrahydro-2-methyl-3-(2-methylphenyl)-4-oxo-6-quinazolinesulfonamide
Mykrox
Zaroxolyn
Diulo
Metolazone(Zaroxolyn)
7-Chloro-2-methyl-4-oxo-3-(o-tolyl)-1,2,3,4-tetrahydroquinazoline-6-sulfonamide
2-Methyl-3-(o-tolyl)-6-sulfamyl-7-chloro-1,2,3,4-tetrahydro-4-quinazolinone
Metenix
Metozalone
Normelan
Oldren
SR 720-22
Xuret
CAS号
17560-51-9
EC号
241-539-3
MDL号
MFCD00069304
PubChem SID
160963869
46509058
24724532
PubChem CID
4170

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 9.535759  质子受体
质子供体 LogD (pH = 5.5) 2.943545 
LogD (pH = 7.4) 2.940775  Log P 2.9435806 
摩尔折射率 94.5879 cm3 极化性 36.030464 Å3
极化表面积 92.5 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 3.21  LOG S -3.95 
溶解度 4.07e-02 g/l 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
60.3 mg/L expand 查看数据来源
Butanol expand 查看数据来源
DMSO: >5 mg/mL expand 查看数据来源
Ethanol expand 查看数据来源
外观
Crystalline Solid expand 查看数据来源
white solid expand 查看数据来源
熔点
248-250°C expand 查看数据来源
252-254°C (dec.) expand 查看数据来源
疏水性(logP)
2.5 expand 查看数据来源
保存条件
-20°C expand 查看数据来源
-20°C Freezer expand 查看数据来源
Room Temperature (15-30°C) expand 查看数据来源
RTECS编号
VA1700000 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
下载链接 expand 查看数据来源
德国WGK号
2 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
相关基因信息
human ... SLC12A1(6557) expand 查看数据来源
纯度
≥98% (HPLC) expand 查看数据来源
95+% 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
Empirical Formula (Hill Notation)
C16H16ClN3O3S 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 -  02153617 external link
Diuretic; anti-hypertensive
DrugBank -  DB00524 external link
Item Information
Drug Groups approved
Description A quinazoline-sulfonamide that is considered a thiazide-like diuretic which is long-acting so useful in chronic renal failure. It also tends to lower blood pressure and increase potassium loss. [PubChem]
Indication For the treatment of hypertension, alone or in combination with other antihypertensive drugs of a different class.
Pharmacology Metolazone is a quinazoline diuretic, with properties generally similar to the thiazide diuretics. A proximal action of metolazone has been shown in humans by increased excretion of phosphate and magnesium ions and by a markedly increased fractional excretion of sodium in patients with severely compromised glomerular filtration. This action has been demonstrated in animals by micropuncture studies.
Toxicity Symptoms of overdose include difficulty breathing, dizziness, dizziness on standing up, drowsiness, fainting, irritation of the stomach and intestines, and lethargy leading to coma.
Affected Organisms
Humans and other mammals
Biotransformation Not substantially metabolized. 70-95% is excreted unchanged in urine via glomerular filtration and active tubular secretion. Undergoes enterohepatic recycling.
Absorption Peak blood levels are obtained within 2 to 4 hours of oral administration. The rate and extent of absorption are formulation dependent.
Half Life Approximately 14 hours.
Protein Binding 50-70% bound to erythrocytes, up to 33% bound to plasma proteins, 2-5% of the drug in circulation is unbound
Elimination Most of the drug is excreted in the unconverted form in the urine.
References
Rosenberg J, Gustafsson F, Galatius S, Hildebrandt PR: Combination therapy with metolazone and loop diuretics in outpatients with refractory heart failure: an observational study and review of the literature. Cardiovasc Drugs Ther. 2005 Aug;19(4):301-6. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com
Selleck Chemicals -  S1610 external link
Research Area: Cardiovascular Disease
Biological Activity:
Metolazone(Zaroxolyn) is primarily used to treat congestive heart failure and high blood pressure. Metolazone indirectly decreases the amount of water reabsorbed into the bloodstream by the kidney, which results in the decreases of blood volume and the increases of urine volume. Metolazone and the other thiazide diuretics inhibit the function of the sodium-chloride symporter and prevent sodium and chloride, water as well, from leaving the lumen to enter the tubule cell. [1]
Sigma Aldrich -  M1195 external link
Biochem/physiol Actions
Inhibitor of thiazide-sensitive Na+-Cl- cotransporter; antihypertensive; moderate "loop" diuretic.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. M1195.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Toronto Research Chemicals -  M338750 external link
A diruetic. An antihypertensive.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Rosenberg J, Gustafsson F, Galatius S, Hildebrandt PR: Combination therapy with metolazone and loop diuretics in outpatients with refractory heart failure: an observational study and review of the literature. Cardiovasc Drugs Ther. 2005 Aug;19(4):301-6. Pubmed
  • http://en.wikipedia.org/wiki/Metolazone
  • Curry, C.L., et al.: Clin. Ther., 9, 47 (1986)
  • Kiyingi, A., et al.: Lancet, 335, 29 (1990)
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专利

专利

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