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9b-amino-4b-hydroxy-7-isopropyl-4b,9b-dihydro-5-oxa-indeno[2,1-a]inden-10-one | 1416231-32-7

中文名称
——
中文别名
——
英文名称
9b-amino-4b-hydroxy-7-isopropyl-4b,9b-dihydro-5-oxa-indeno[2,1-a]inden-10-one
英文别名
9b-amino-4b-hydroxy-7-isopropyl-4-bH-benzo[d]indeno[1,2-b]furan-10(9bH)-one;9b-Amino-4b-hydroxy-7-isopropyl-4b,9b-dihydro-5-oxa-indeno[2,1-a]inden-10-one;9b-amino-4b-hydroxy-7-propan-2-ylindeno[1,2-b][1]benzofuran-10-one
9b-amino-4b-hydroxy-7-isopropyl-4b,9b-dihydro-5-oxa-indeno[2,1-a]inden-10-one化学式
CAS
1416231-32-7
化学式
C18H17NO3
mdl
——
分子量
295.338
InChiKey
HIERACINAHKHJR-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

物化性质

  • 沸点:
    475.2±45.0 °C(Predicted)
  • 密度:
    1.378±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    72.6
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
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    • 2
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    • 4
    • 5
    • 6

反应信息

  • 作为反应物:
    描述:
    9b-amino-4b-hydroxy-7-isopropyl-4b,9b-dihydro-5-oxa-indeno[2,1-a]inden-10-oneN,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 、 三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 18.01h, 生成 2-amino-N-(4b-hydroxy-7-isopropyl-10-oxo-4b,10-dihydro-9bH-indeno[1,2-b]benzofuran-9b-yl)acetamide
    参考文献:
    名称:
    NOVEL COMPOUND, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF VIRAL DISEASES CONTAINING SAME AS ACTIVE INGREDIENT
    摘要:
    公开号:
    EP2933254B1
  • 作为产物:
    参考文献:
    名称:
    INDANONE DERIVATIVES, PHARMACEUTICALLY ACCEPTABLE SALTS OR OPTICAL ISOMERS THEREOF, PREPARATION METHOD FOR SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME AS ACTIVE INGREDIENT FOR PREVENTING OR TREATING VIRAL DISEASES
    摘要:
    揭示了新颖的茚酮衍生物,其药用盐或对映体,以及其制备方法和作为活性成分的用于预防或治疗病毒性疾病的药物组合物。这些茚酮衍生物对包括柯萨奇病毒、肠道病毒、回声病毒、脊髓灰质炎病毒和鼻病毒在内的小RNA病毒具有出色的抑制活性,并且具有低细胞毒性,因此它们可用作预防或治疗包括小儿麻痹症、瘫痪、急性出血性结膜炎、病毒性脑膜炎、手足口病、水疱病、甲型肝炎、肌炎、心肌炎、胰腺炎、糖尿病、流行性肌痛、脑炎、流感、手足口病、哮喘、慢性阻塞性肺病、肺炎、鼻窦炎或中耳炎等病毒性疾病的药物组合物的活性成分。
    公开号:
    US20140114068A1
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文献信息

  • NOVEL COMPOUND, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, METHOD FOR PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF VIRAL DISEASES CONTAINING SAME AS ACTIVE INGREDIENT
    申请人:KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
    公开号:US20150336920A1
    公开(公告)日:2015-11-26
    The present invention relates to a novel compound, to a pharmaceutically acceptable salt or optical isomer thereof, to a method for preparing same, and to a pharmaceutical composition for the prevention or treatment of viral diseases containing same as an active ingredient. The novel compound according to the present invention not only has low cytotoxicity but also has excellent antiviral activity against picornavirus such as coxsackievirus, enterovirus, echovirus, poliovirus and rhinovirus, and thus can be effectively used as a pharmaceutical composition for the prevention or treatment of viral diseases such as infantile paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand-foot-and-mouth disease, vesicular disease, hepatitis A, myitis, myocarditis, pancreatitis, diabetes, epidemic myalgia, encephalitis, cold, herpangina, foot-and-mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinus infection, or otitis media.
    本发明涉及一种新型化合物,一种药学上可接受的盐或其光学异构体,一种制备方法,以及一种包含其作为活性成分的用于预防或治疗病毒性疾病的制药组合物。本发明的新型化合物不仅细胞毒性低,而且对柯萨奇病毒、肠道病毒、回肠病毒、脊髓灰质炎病毒和鼻病毒等小RNA病毒具有出色的抗病毒活性,因此可以有效地用作预防或治疗儿童麻痹症、急性出血性结膜炎、病毒性脑膜炎、手足口病、水痘、甲型肝炎、肌炎、心肌炎、胰腺炎、糖尿病、流行性肌痛、脑炎、感冒、疱疹咽峡炎、口蹄疫、哮喘、慢性阻塞性肺病、肺炎、鼻窦炎或中耳炎的制药组合物。
  • 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient
    申请人:Jung Young Sik
    公开号:US09346749B2
    公开(公告)日:2016-05-24
    Disclosed are 1,3-Dioxoindene derivatives, pharmaceutically acceptable salts thereof or enantiomers, a preparation method thereof, and a pharmaceutical composition for the prevention or treatment of viral diseases, comprising the same as an active ingredient. The 1,3-Dioxoindene derivatives have excellent inhibitory activity against picornaviruses including coxsackie-, entero-, echo-, Polio-, and rhinoviruses, as well as exhibiting low cytotoxicity, so that they can be useful as an active ingredient of a pharmaceutical composition for the prevention or treatment of viral diseases including poliomyelitis, paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand-foot-and-mouth disease, vesicular disease, hepatitis A, myositis, myocarditis, pancreatitis, diabetes, epidemic myalgia, encephalitis, flu, herpangina, foot-and-mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
    本发明涉及1,3-二氧吲哚衍生物、其药学上可接受的盐或对映体、其制备方法以及用作预防或治疗病毒性疾病的制药组合物,其中包括该衍生物作为活性成分。该1,3-二氧吲哚衍生物对小肠病毒科病毒(包括柯萨奇病毒、肠道病毒、回声病毒、脊髓灰质炎病毒和鼻病毒)具有优异的抑制活性,并且表现出低细胞毒性,因此可以作为预防或治疗病毒性疾病的制药组合物的活性成分,包括小儿麻痹症、瘫痪、急性出血性结膜炎、病毒性脑膜炎、手足口病、水疱性疾病、甲型肝炎、肌炎、心肌炎、胰腺炎、糖尿病、流行性肌痛、脑炎、流感、咽峡炎、口腔疱疹、口蹄疫、哮喘、慢性阻塞性肺疾病、肺炎、鼻窦炎或中耳炎。
  • COMPOUND, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF VIRAL DISEASES CONTAINING SAME AS ACTIVE INGREDIENT
    申请人:Korea Research Institute of Chemical Technology
    公开号:EP3882244A1
    公开(公告)日:2021-09-22
    The present invention relates to a novel compound, to a pharmaceutically acceptable salt or optical isomer thereof, to a method for preparing same, and to a pharmaceutical composition for the prevention or treatment of viral diseases containing same as an active ingredient. The novel compound according to the present invention not only has low cytotoxicity but also has excellent antiviral activity against picornavirus such as coxsackievirus, enterovirus, echovirus, poliovirus and rhinovirus, and thus can be effectively used as a pharmaceutical composition for the prevention or treatment of viral diseases such as infantile paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand-foot-and-mouth disease, vesicular disease, hepatitis A, myitis, myocarditis, pancreatitis, diabetes, epidemic myalgia, encephalitis, cold, herpangina, foot-and-mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinus infection, or otitis media.
    本发明涉及一种新型化合物、其药学上可接受的盐或光学异构体、其制备方法以及以其为活性成分的预防或治疗病毒性疾病的药物组合物。根据本发明的新型化合物不仅细胞毒性低,而且对柯萨奇病毒、肠道病毒、埃可病毒、脊髓灰质炎病毒和鼻病毒等皮卡病毒具有优异的抗病毒活性,因此可有效地用作预防或治疗婴儿麻痹等病毒性疾病的药物组合物、急性出血性结膜炎、病毒性脑膜炎、手足口病、水泡病、甲型肝炎、肌炎、心肌炎、胰腺炎、糖尿病、流行性肌痛、脑炎、感冒、疱疹、口蹄疫、哮喘、慢性阻塞性肺病、肺炎、鼻窦炎或中耳炎。
  • 1,3-DI-OXO-INDENE DERIVATIVE, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ANTIVIRAL, ACTIVE INGREDIENT
    申请人:Korea Research Institute of Chemical Technology
    公开号:EP2722322B8
    公开(公告)日:2020-03-11
  • US9346749B2
    申请人:——
    公开号:US9346749B2
    公开(公告)日:2016-05-24
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