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Valsartan and hydrochlorothiazide | 186615-83-8

中文名称
——
中文别名
——
英文名称
Valsartan and hydrochlorothiazide
英文别名
6-chloro-1,1-dioxo-3,4-dihydro-2H-1λ6,2,4-benzothiadiazine-7-sulfonamide;(2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoic acid
Valsartan and hydrochlorothiazide化学式
CAS
186615-83-8
化学式
C31H37ClN8O7S2
mdl
——
分子量
733.3
InChiKey
UIYUUEDFAMZISF-FTBISJDPSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.81
  • 重原子数:
    49
  • 可旋转键数:
    11
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    247
  • 氢给体数:
    5
  • 氢受体数:
    13

反应信息

  • 作为产物:
    参考文献:
    名称:
    REDUCING ER STRESS IN THE TREATMENT OF OBESITY AND DIABETES
    摘要:
    内质网应激与肥胖有关。因此,减少或防止内质网应激的药物可用于治疗与肥胖相关的疾病,包括外周胰岛素抵抗、高血糖和2型糖尿病。已经显示出减少内质网应激并降低血糖水平的两种化合物包括4-苯基丁酸(PBA)、牛磺胆酸(TUDCA)和三甲胺氧化物(TMAO)。其他有用于减少内质网应激的化合物是化学分子伴侣,例如三甲胺氧化物和甘油。本发明提供了使用内质网应激减轻剂如PBA、TUDCA和TMAO治疗患有肥胖、高血糖、2型糖尿病或胰岛素抵抗的受试者的方法。还提供了通过识别减少内质网应激标志物水平的药物筛选内质网应激减轻剂的方法。这些药物可用于治疗与肥胖相关的疾病的方法和制药组合物。
    公开号:
    US20100075894A1
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文献信息

  • Method for treating resistant hypertension
    申请人:Gerber Michael J.
    公开号:US20070196510A1
    公开(公告)日:2007-08-23
    A method is provided for lowering blood pressure in a patient having clinically diagnosed resistant hypertension. The method comprises administering darusentan to the patient adjunctively with a baseline antihypertensive regimen that comprises administration of at least one diuretic and at least two antihypertensive drugs selected from at least two of (a) ACE inhibitors and angiotensin II receptor blockers, (b) beta-adrenergic receptor blockers and (c) calcium channel blockers. The darusentan is orally administered at a dose and frequency effective, in combination with the baseline regimen, to provide a reduction of at least about 3 mmHg in one or more blood pressure parameters selected from trough sitting systolic, trough sitting diastolic, 24-hour ambulatory systolic, 24-hour ambulatory diastolic, maximum diurnal systolic and maximum diurnal diastolic blood pressures.
    提供了一种降低临床诊断为顽固性高血压患者血压的方法。该方法包括将达卢生坦作为辅助药物与基础抗高血压治疗方案联合给药,该基础方案包括至少一种利尿剂和至少两种抗高血压药物,这些药物选自至少两类:(a) ACE抑制剂和血管紧张素II受体阻滞剂,(b) β-肾上腺素能受体阻滞剂,以及(c) 钙通道阻滞剂。达卢生坦以有效剂量和频率口服给药,与基础治疗方案结合,能够使选自谷值坐位收缩压、谷值坐位舒张压、24小时动态收缩压、24小时动态舒张压、日间最高收缩压和日间最高舒张压的一个或多个血压参数至少降低约3 mmHg。
  • [EN] POLYBIOTIN COMPOUNDS FOR MAGNETIC RESONANCE IMAGINING AND DRUG DELIVERY<br/>[FR] COMPOSES DE POLYBIOTINE POUR IRM ET ADMINISTRATION DE MEDICAMENTS
    申请人:GEN HOSPITAL CORP
    公开号:WO2005032598A1
    公开(公告)日:2005-04-14
    The invention relates generally to biotin-containing compounds that are useful as imaging agents and drug-delivery agents. Another aspect of the invention relates to the aforementioned compounds chelated to a metal atom. In a preferred embodiment, the metal atom is a gadolinium. Another aspect of the invention relates to a compound comprising three biotin moieties and a pharmaceutical agent covalently bound to a heterocyclic core. In certain embodiments, the pharmaceutical agent is an antibiotic, antiviral, or radionuclide. Another aspect of the present invention relates to a method of treating disease involving administering the compounds of the invention to a mammal. Another aspect of the present invention relates to a method of acquiring a magnetic resonance image using the compounds of the invention.
    该发明涉及一般用作成像剂和药物传递剂的含生物素化合物。该发明的另一个方面涉及上述化合物螯合到金属原子上。在一个优选实施例中,金属原子是钆。该发明的另一个方面涉及一种包含三个生物素基团和一个与杂环核共价结合的药物剂的化合物。在某些实施例中,药物剂是抗生素、抗病毒药物或放射性核素。本发明的另一个方面涉及一种涉及向哺乳动物施用该发明化合物以治疗疾病的方法。本发明的另一个方面涉及使用该发明化合物获得磁共振图像的方法。
  • THERAPY FOR COMPLICATIONS OF DIABETES
    申请人:Roden Robert L.
    公开号:US20090054473A1
    公开(公告)日:2009-02-26
    A method for enhancing glycemic control and/or insulin sensitivity in a human subject having diabetic nephropathy and/or metabolic syndrome comprises administering to the subject a selective endothelin A (ET A ) receptor antagonist in a glycemic control and/or insulin sensitivity enhancing effective amount. A method for treating a complex of comorbidities in an elderly diabetic human subject comprises administering to the subject a selective ET A receptor antagonist in combination or as adjunctive therapy with at least one additional agent that is (i) other than a selective ET A receptor antagonist and (ii) effective in treatment of diabetes and/or at least one of said comorbidities other than hypertension. A therapeutic combination useful in such a method comprises a selective ET A receptor antagonist and at least one antidiabetic, anti-obesity or antidyslipidemic agent other than a selective ET A receptor antagonist.
    一种增强患有糖尿病肾病和/或代谢综合征的人类受试者的血糖控制和/或胰岛素敏感性的方法,包括向该受试者施用一种选择性内皮素A(ETA)受体拮抗剂,其剂量足以增强血糖控制和/或胰岛素敏感性。一种治疗老年糖尿病人类受试者中复合共病的方法,包括向该受试者施用一种选择性ETA受体拮抗剂,与至少一种其他药物联合或作为辅助治疗,该其他药物(i)不是选择性ETA受体拮抗剂,且(ii)在治疗糖尿病和/或至少一种除高血压外的上述共病中有效。适用于此类方法的治疗组合包括一种选择性ETA受体拮抗剂和至少一种非选择性ETA受体拮抗剂的抗糖尿病、抗肥胖或抗血脂异常药物。
  • ANTIHYPERTENSIVE THERAPY
    申请人:Gerber Michael J.
    公开号:US20090221549A1
    公开(公告)日:2009-09-03
    A new use of darusentan is provided in preparation of a pharmaceutical composition for lowering blood pressure in a patient exhibiting resistance to a baseline antihypertensive therapy with one or more drugs. The composition comprises darusentan in an amount providing a therapeutically effective daily dose; wherein (a) the composition is orally deliverable and/or (b) the daily dose of darusentan is effective to provide a reduction of at least about 3 mmHg in one or more blood pressure parameters selected from trough sitting systolic, trough sitting diastolic, 24-hour ambulatory systolic, 24-hour ambulatory diastolic, maximum diurnal systolic and maximum diurnal diastolic blood pressures. Further provided is a new use of darusentan in preparation of a pharmaceutical composition for lowering blood pressure in a patient exhibiting resistance to a baseline antihypertensive therapy, wherein the composition is administered adjunctively with at least one diuretic and at least one antihypertensive drug selected from ACE inhibitors, angiotensin II receptor blockers, beta-adrenergic receptor blockers and calcium channel blockers.
    提供了一种新的达卢生坦用途,用于制备一种药用组合物,旨在降低对一种或多种药物的基础抗高血压治疗表现出抵抗性的患者的血压。该组合物包含达卢生坦,其剂量提供了治疗上有效的每日剂量;其中(a)该组合物可通过口服给药,和/或(b)达卢生坦的每日剂量有效,能在一项或多项选自谷底坐位收缩压、谷底坐位舒张压、24小时动态收缩压、24小时动态舒张压、日间最高收缩压和日间最高舒张压的血压参数中至少降低约3mmHg。还提供了一种新的达卢生坦用途,用于制备一种药用组合物,旨在降低对基础抗高血压治疗表现出抵抗性的患者的血压,其中该组合物与至少一种利尿剂和至少一种选自ACE抑制剂、血管紧张素II受体阻滞剂、β-肾上腺素能受体阻滞剂和钙通道阻滞剂的抗高血压药物联合给药。
  • Polybiotin compounds for magnetic resonance imaging and drug delivery
    申请人:Elmaleh R. David
    公开号:US20050136008A1
    公开(公告)日:2005-06-23
    The invention relates generally to biotin-containing compounds that are useful as imaging agents and drug-delivery agents. Another aspect of the invention relates to the aforementioned compounds chelated to a metal atom. In a preferred embodiment, the metal atom is a gadolinium. Another aspect of the invention relates to a compound comprising three biotin moieties and a pharmaceutical agent covalently bound to a heterocyclic core. In certain embodiments, the pharmaceutical agent is an antibiotic, antiviral, or radionuclide. Another aspect of the present invention relates to a method of treating disease involving administering the compounds of the invention to a mammal. Another aspect of the present invention relates to a method of acquiring a magnetic resonance image using the compounds of the invention.
    本发明涉及一般用作成像剂和药物传递剂的含生物素化合物。本发明的另一方面涉及上述化合物与金属原子螯合的化合物。在一种首选实施方式中,金属原子是钆。本发明的另一方面涉及一种化合物,其包括三个生物素基团和与杂环核共价结合的药物剂。在某些实施方式中,药物剂是抗生素、抗病毒药物或放射性核素。本发明的另一方面涉及一种将本发明化合物用于治疗哺乳动物疾病的方法。本发明的另一方面涉及使用本发明化合物获得磁共振图像的方法。
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同类化合物

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