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1-(1-methyl-1H-imidazol-5-yl)propan-1-one | 592555-22-1

中文名称
——
中文别名
——
英文名称
1-(1-methyl-1H-imidazol-5-yl)propan-1-one
英文别名
1-(3-methylimidazol-4-yl)propan-1-one
1-(1-methyl-1H-imidazol-5-yl)propan-1-one化学式
CAS
592555-22-1
化学式
C7H10N2O
mdl
MFCD18811107
分子量
138.169
InChiKey
QZUSGFQVNBUUPC-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):
    0.5
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    34.9
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Imidazole derivatives, production method thereof and use thereof
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1681290B9
    公开(公告)日:2013-06-19
  • FUSED HETEROCYCLIC COMPOUNDS AS SODIUM CHANNEL MODULATORS
    申请人:Gilead Sciences, Inc.
    公开号:EP2707361B1
    公开(公告)日:2017-08-23
  • 17-Heterocyclic-4-azasteroid derivatives as androgen receptor modulators
    申请人:Kaufman L. Mildred
    公开号:US20070054933A1
    公开(公告)日:2007-03-08
    Compounds of structural formula I are modulators of the androgen receptor (AR) in a tissue selective manner. These compounds are useful in the enhancement of weakened muscle tone and the treatment of conditions caused by androgen deficiency or which can be ameliorated by androgen administration, including osteoporosis, osteopenia, glucocorticoid-induced osteoporosis, periodontal disease, bone fracture, bone damage following bone reconstructive surgery, sarcopenia, frailty, aging skin, male hypogonadism, postmenopausal symptoms in women, atherosclerosis, hypercholesterolemia, hyperlipidemia, obesity, aplastic anemia and other hematopoietic disorders, inflammatory arthritis and joint repair, HIV-wasting, prostate cancer, benign prostatic hyperplasia (BPH), abdominal adiposity, metabolic syndrome, type II diabetes, cancer cachexia, Alzheimer's disease, muscular dystrophies, cognitive decline, sexual dysfunction, sleep apnea, depression, premature ovarian failure, and autoimmune disease, alone or in combination with other active agents.
  • LINKED DIBENZIMIDAZOLE DERIVATIVES
    申请人:Or Yat Sun
    公开号:US20100221214A1
    公开(公告)日:2010-09-02
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
  • LINKED DIIMIDAZOLE DERIVATIVES
    申请人:Qiu Yao-Ling
    公开号:US20100226883A1
    公开(公告)日:2010-09-09
    The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
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