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3-propionylbenzenesulfonamide | 210826-98-5

中文名称
——
中文别名
——
英文名称
3-propionylbenzenesulfonamide
英文别名
3-propanoylbenzenesulfonamide
3-propionylbenzenesulfonamide化学式
CAS
210826-98-5
化学式
C9H11NO3S
mdl
——
分子量
213.257
InChiKey
SPAVECFGRZAWSI-UHFFFAOYSA-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):
    0.7
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    85.6
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • 7-MEMBERED RING COMPOUND AND METHOD OF PRODUCTION AND PHARMACEUTICAL APPLICATION THEREOF
    申请人:Muto Tsuyoshi
    公开号:US20090253683A1
    公开(公告)日:2009-10-08
    A 7-membered heterocyclic compound having the formula (I), or its salt, or a solvate thereof with a chymase inhibitory action and useful for the prevention or treatment of various diseases, in which chymase is involved: a method for producing the same, and a pharmaceutical composition useful for the prevention or treatment of diseases, in which chymase is involved, including the compound of having the formula (I), or its pharmaceutically acceptable salt, or a solvate thereof are provided.
    本发明提供一种具有式(I)的7元杂环化合物或其盐或其溶剂合物,具有抑制chymase的作用,用于预防或治疗各种涉及chymase的疾病的方法,以及用于预防或治疗各种涉及chymase的疾病的药物组合物,包括具有式(I)的化合物或其药学上可接受的盐或其溶剂合物的药物组合物。
  • 4-Substituted furan-2-sulfonamide and its use in the preparation of sulfonyl urea derivatives
    申请人:PFIZER INC.
    公开号:EP1270565A1
    公开(公告)日:2003-01-02
    The invention relates to a compound, 4-(1-hydroxy-1-methyl-ethyl)furan-2-sulfonamide, and its use as an intermediate in the preparation of a compound of the formula wherein R1 and R2 are as defined in the description, useful in the treatment and condition selected from the group consisting of meningitis and salpingitis, septic shock, disseminated intravascular coagulation, and/or adult respiratory distress syndrome, acute or chronic inflammation, arthritis, cholangitis, colitis, encephalitis, endocarditis, glomerulonephritis, hepatitis, myocarditis, pancreatitis, pericarditis, reperfusion injury, vasculitis, acute and delayed hypersensitivity, graft rejection, and graft-versus-host disease, auto-immune diseases including Type 1 diabetes mellitus and multiple sclerosis, periodonate diseases, interstitial pulmonary fibrosis, cirrhosis, systemic sclerosis, keloid formation, tumors which produce IL-1 as an autocrine growth factor, cachexia, Alzheimers disease, percussion injury, depression, atherosclerosis (including cardiomyopathy, myocarditis and heart failure) and osteoporosis in a mammal, including a human.
    本发明涉及一种化合物,4-(1-羟基-1-甲基-乙基)呋喃-2-磺酰胺,及其在制备 式化合物中作为中间体的用途,其中 R1 和 R2 如描述中所定义。 其中 R1 和 R2 如描述中所定义,可用于治疗选自以下组别的疾病:脑膜炎和输卵管炎、脓毒性休克、弥散性血管内凝血和/或成人呼吸窘迫综合征、急性或慢性炎症、关节炎、胆管炎、结肠炎、脑炎、心内膜炎、肾小球肾炎、肝炎、心肌炎、胰腺炎、心包炎、再灌注损伤、血管炎、急性和迟发性超敏反应、移植物排斥和移植物抗宿主疾病、自身免疫性疾病(包括 1 型糖尿病和多发性硬化症)、牙周病、间质性肺纤维化、肝硬化、系统性硬化症、瘢痕疙瘩的形成、产生 IL-1 作为自分泌生长因子的肿瘤、恶病质、老年痴呆症、叩击伤、抑郁症、动脉粥样硬化(包括心肌病、心肌炎和心力衰竭)以及哺乳动物(包括人类)骨质疏松症。
  • Sulfonyl urea derivatives and their use in the control of interleukin-1 activity
    申请人:PFIZER INC.
    公开号:EP1270554A1
    公开(公告)日:2003-01-02
    The invention relates to a compound of the formula wherein R1 and R2 are as defined in the description, useful in the treatment and condition selected from the group consisting of meningitis and salpingitis, septic shock, disseminated intravascular coagulation, and/or adult respiratory distress syndrome, acute or chronic inflammation, arthritis, cholangitis, colitis, encephalitis, endocarditis, glomerulonephritis, hepatitis, myocarditis, pancreatitis, pericarditis, reperfusion injury, vasculitis, acute and delayed hypersensitivity, graft rejection, and graft-versus-host disease, auto-immune diseases including Type 1 diabetes mellitus and multiple sclerosis, periodonate diseases, interstitial pulmonary fibrosis, cirrhosis, systemic sclerosis, keloid formation, tumors which produce IL-1 as an autocrine growth factor, cachexia, Alzheimers disease, percussion injury, depression, atherosclerosis (including cardiomyopathy, myocarditis and heart failure) and osteoporosis in a mammal, including a human.
    本发明涉及一种如下式的化合物 其中 R1 和 R2 如描述中所定义,可用于治疗选自以下组别的疾病:脑膜炎和输卵管炎、脓毒性休克、弥散性血管内凝血和/或成人呼吸窘迫综合征、急性或慢性炎症、关节炎、胆管炎、结肠炎、脑炎、心内膜炎、肾小球肾炎、肝炎、心肌炎、胰腺炎、心包炎、再灌注损伤、血管炎、急性和迟发性超敏反应、移植物排斥和移植物抗宿主疾病、自身免疫性疾病(包括 1 型糖尿病和多发性硬化症)、牙周病、间质性肺纤维化、肝硬化、系统性硬化症、瘢痕疙瘩的形成、产生 IL-1 作为自分泌生长因子的肿瘤、恶病质、老年痴呆症、叩击伤、抑郁症、动脉粥样硬化(包括心肌病、心肌炎和心力衰竭)以及哺乳动物(包括人类)骨质疏松症。
  • SEVEN-MEMBERED RING COMPOUND, PRODUCTION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF
    申请人:Asubio Pharma Co., Ltd.
    公开号:EP2025672A1
    公开(公告)日:2009-02-18
    A 7-membered heterocyclic compound having the formula (I), or its salt, or a solvate thereof with a chymase inhibitory action and useful for the prevention or treatment of various diseases, in which chymase is involved: a method for producing the same, and a pharmaceutical composition useful for the prevention or treatment of diseases, in which chymase is involved, including the compound of having the formula (I), or its pharmaceutically acceptable salt, or a solvate thereof are provided.
    本发明提供了一种具有式 (I) 的 7 元杂环化合物,或其盐,或其溶液,具有糜蛋白酶抑制作用,可用于预防或治疗涉及糜蛋白酶的各种疾病:一种生产该化合物的方法,以及一种用于预防或治疗涉及糜蛋白酶的疾病的药物组合物,包括具有式 (I) 的化合物,或其药学上可接受的盐,或其溶液。
  • Aminomethyl-substituted aromatic acids as intermediates for the preparation of chymase inhibiting 1,4-diazepan-2,5-dione compounds
    申请人:Daiichi Sankyo Company, Limited
    公开号:EP2463268A1
    公开(公告)日:2012-06-13
    A compound, or its salt or a solvate thereof, having the formula (Va): for producing a 7-membered heterocyclic compound, or its salt or a solvate thereof having formula (I): the compound of formula (I) having a chymase inhibitory action and useful for the prevention or treatment of various diseases in which chymase is involved and a method of producing a compound of formula (I) from a compound of formula (Va) are provided.
    具有式 (Va) 的化合物或其盐或溶液: 用于生产式(I)的 7 元杂环化合物或其盐或其溶液: 本发明提供了具有糜蛋白酶抑制作用并可用于预防或治疗涉及糜蛋白酶的各种疾病的式 (I) 化合物,以及由式 (Va) 化合物生产式 (I) 化合物的方法。
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