CAS: 148-56-1; 1,1-Dioxo-6-(Trifluoromethyl)-4H-1λ6,2,4-Benzothiadiazine-7-Sulfonamide

该化合物是治疗高血压和与各种医疗条件有关的水肿时常用的硫酸二甲酸二甲酸,它的作用是抑制钠在甲壳体分解管管内重新吸附,导致钠和水的排泄增加,从而减少了血量和血压.氟甲酰胺的化学结构包括一个硫酸亚甲酯环,这是这一类糖尿病的特征,通常以口服形式施用.氟甲酰胺与其他二甲胺相比,其作用时间相对较长,使其能有效地管理慢性病.它也可能产生副作用,包括电解不平衡,特别是低血糖,而且应谨慎地用于肾损伤的病人.此外,它可能与其他药物相互作用,需要仔细监测.

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      专利信息


      专利号:US-2007287734-A1
      优先权日:2006-06-09
      标 题 :Preparation and utility of substituted pyrazole compounds with cannabinoid receptor activity
      发明人:GANT THOMAS G; SARSHAR SEPEHR
      权利人:AUSPEX PHARMACEUTICALS INC
      摘要:The present disclosure is directed to modulators of CB-1 type receptors and pharmaceutically acceptable salts and prodrugs thereof, the chemical synthesis thereof, and the medical use of such compounds for the treatment and/or management of the severity and duration of obesity, metabolic syndrome, dyslipidemia, glucose imbalance, the inability to maintain weight loss, insulin resistance, a cardiovascular disorder, memory loss, drug dependence, a depressive disorder, a panic disorder, an obsessive-compulsive disorder, anxiety, post-traumatic stress syndrome, and any other condition in which it is beneficial to inhibit, inversely agonize or modulate a cannabinoid receptor are described.

      专利号:US-2007276042-A1
      优先权日:2006-05-26
      标题:Preparation and utility of substituted carboxylic acid compounds
      发明人:GANT THOMAS G; SARSHAR SEPEHR; WOO SOON HYUNG
      权利人:AUSPEX PHARMACEUTICALS INC
      摘要:The present disclosure is directed to modulators of cyclooxygenase (COX) enzymes and pharmaceutically acceptable salts and prodrugs thereof, the chemical synthesis thereof, and the medical use of such compounds for the treatment and/or management of the severity and duration of non-specific pain, tension-type pain, headache, migraine, lower back pain, sciatica, dental pain, muscular pain, pain associated with acute soft tissue injuries, bursitis, tendonitis, lumbago, periarthritis, tennis elbow, sprains, strains, muscular problems associated with sports injuries, muscular problems associated with accidents, period pain, primary dysmenorrhoea, acute sore throat pain, osteoarthritis, rheumatoid arthritis, cancer, any disorder requiring analgesic response, any disorder requiring anti-inflammatory response, any disorder requiring antipyretic response, any conditions mediated by cyclooxygenase, cystic fibrosis, dementia, Alzheimer's disease, and/or conditions mediated by levels of β-amyloid are described.

      专利号:US-10906888-B2
      优先权日:2016-07-14
      标 题:Pyrimidine carboxamides as inhibitors of Vanin-1 enzyme
      发明人:CASIMIRO-GARCIA AGUSTIN; STROHBACH JOSEPH WALTER; HEPWORTH DAVID; LOVERING FRANK ELDRIDGE; CHOI CHULHO; ALLAIS CHRISTOPHE PHILIPPE; WRIGHT STEPHEN WAYNE
      权利人:PFIZER
      摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

      专利号:US-10968192-B2
      优先权日:2018-09-26
      标题:Crystalline solid forms of N-(1-((2-(dimethylamino)ethyl)amino)-2-methyl-1-oxopropan-2-yl)-4-(4-(2-methyl-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(methylthio)tetrahydro-2H-pyran-2-yl)benzyl)phenyl)butanamide and methods of their synthesis
      发明人:BEDNARZ MARK STEPHEN; Dai Kuangchu; ECKERT JEFFREY MANNING; LIM NGIAP-KIE; SIROIS LAUREN; WU WENXUE; ZHAO MATTHEW MANGZHU
      权利人:LEXICON PHARMACEUTICALS INC
      摘要:Methods of preparing, and solid forms of N-(1-((2-(dimethylamino)ethyl)amino)-2-methyl-1-oxopropan-2-yl)-4-(4-(2-methyl-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(methylthio)tetrahydro-2H-pyran-2-yl)benzyl)phenyl)butanamide, and salts, solvates and cocrystals thereof, are disclosed.

      专利号:US-2008039473-A1
      优先权日:2006-08-08
      标题:Preparation and utility of substituted quinazoline compounds with alpha-adrenergic blocking effects
      发明人:GANT THOMAS G; SARSHAR SEPEHR
      权利人:AUSPEX PHARMACEUTICALS INC
      摘要:The present disclosure is directed to modulators of alpha-adrenergic receptors and pharmaceutically acceptable salts and prodrugs thereof, the chemical synthesis thereof, and the use of such compounds for the treatment and/or management of hypertension, cardiac failure, prostatitis, and benign prostatic hyperplasia, and any other condition in which it is beneficial to modulate an alpha-adrenergic receptor.

      专利号:US-8101633-B2
      优先权日:2006-06-05
      标 题 :Preparation and utility of substituted imidazopyridine compounds with hypnotic effects
      发明人:GANT THOMAS G; SARSHAR SEPEHR
      权利人:GANT THOMAS G; SARSHAR SEPEHR; AUSPEX PHARMACEUTICALS INC
      摘要:The present disclosure is directed to modulators of GABA A receptors and pharmaceutically acceptable salts and prodrugs thereof, the chemical synthesis thereof, and the medical use of such compounds for the treatment and/or management of sleep disorders and/or for providing a patient in need with a hypnotic, anxiolytic or anti-convulsive effect are described.

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      主要参考文献


      1: Khodakivs'kyĭ OA. [Characteristics of antiischemic and nootropic properties of ademol in a rat model of acute brain ischemia]. Fiziol Zh. 2013;59(5):71-7. Ukrainian. Ukrainian.
      10: POUTSIAKA JW, PIALA JJ, SMITH CI, BURKE JC, THOMAS BG. Pharmacologic studies of flumethiazide (ademol). J Pharmacol Exp Ther. 1960 Apr;128:405-13. Mil Med. 1959 Aug;124(8):584-90.

      合成参考文献


      摘要:Sunshine, I. (ed.). CRC Handbook of Analytical Toxicology. Cleveland: The Chemical Rubber Co., 1969., p. 768
      摘要:Goodman, L.S., and A. Gilman. (eds.) The Pharmacological Basis of Therapeutics. 5th ed. New York: Macmillan Publishing Co., Inc., 1975., p. 832
      摘要:Goodman, L.S., and A. Gilman. (eds.) The Pharmacological Basis of Therapeutics. 5th ed. New York: Macmillan Publishing Co., Inc., 1975., p. 831
      摘要:The Merck Index. 9th ed. Rahway, New Jersey: Merck & Co., Inc., 1976., p. 535
      摘要:Goodman, L.S., and A. Gilman. (eds.) The Pharmacological Basis of Therapeutics. 5th ed. New York: Macmillan Publishing Co., Inc., 1975., p. 828
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