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1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone | 1215085-77-0

中文名称
——
中文别名
——
英文名称
1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone
英文别名
1-(4-fluorophenyl)-2-prop-2-enoxyethanone
1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone化学式
CAS
1215085-77-0
化学式
C11H11FO2
mdl
——
分子量
194.206
InChiKey
YBXWRUCZVHMHCK-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    potassium cyanide1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone 、 ammonium carbonate monohydrate 在 作用下, 以 乙醇 为溶剂, 反应 22.0h, 生成 4-(4-fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidine-2,5-dione
    参考文献:
    名称:
    Identification of a 4-(Hydroxymethyl)diarylhydantoin as a Selective Androgen Receptor Modulator
    摘要:
    Structural modification performed on a 4-methyl-4-(4-hydroxyphenyphyl)hydantoin series is described which resulted in the development of a new series of 4-(hydroxymethyl)diarylhydantoin analogues as potent, partial agonists of the human androgen receptor. This led to the identification of (S)-(-)-4-(4-(hydroxymethyl)-3-methyl-2,5-dioxo-4-phenylimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile ((S)-(-)-18a, GLPG0492) evaluated in vivo in a classical model of orchidectomized rat. In this model, (-)-18a exhibited anabolic activity on muscle, strongly dissociated from the androgenic activity on prostate after oral dosing. (-)-18a has very good pharmacokinetic properties, including bioavailability in rat (F > 50%), and is currently under evaluation in phase I clinical trials.
    DOI:
    10.1021/jm300281x
  • 作为产物:
    描述:
    2-溴-4'-氟苯乙酮calcium sulfate 、 sodium formate 、 silver(l) oxide 作用下, 以 乙醇 为溶剂, 生成 1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone
    参考文献:
    名称:
    Identification of a 4-(Hydroxymethyl)diarylhydantoin as a Selective Androgen Receptor Modulator
    摘要:
    Structural modification performed on a 4-methyl-4-(4-hydroxyphenyphyl)hydantoin series is described which resulted in the development of a new series of 4-(hydroxymethyl)diarylhydantoin analogues as potent, partial agonists of the human androgen receptor. This led to the identification of (S)-(-)-4-(4-(hydroxymethyl)-3-methyl-2,5-dioxo-4-phenylimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile ((S)-(-)-18a, GLPG0492) evaluated in vivo in a classical model of orchidectomized rat. In this model, (-)-18a exhibited anabolic activity on muscle, strongly dissociated from the androgenic activity on prostate after oral dosing. (-)-18a has very good pharmacokinetic properties, including bioavailability in rat (F > 50%), and is currently under evaluation in phase I clinical trials.
    DOI:
    10.1021/jm300281x
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文献信息

  • [EN] NOVEL IMIDAZOLIDINE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS<br/>[FR] NOUVEAUX COMPOSÉS D'IMIDAZOLIDINE EN TANT QUE MODULATEURS DU RÉCEPTEUR D'ANDROGÈNE
    申请人:GALAPAGOS NV
    公开号:WO2010029119A1
    公开(公告)日:2010-03-18
    Novel compounds are disclosed that have a Formula represented by the following: wherein X, R1, R2a, R2b, R2c, R3a R3b, R4a, R4b, R4c, and ml are as described herein. The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non- limiting example, cachexia, osteoporosis, sarcopenia, a decline in libido and/or sexual dysfunction.
    揭示了具有以下公式表示的新化合物:其中X、R1、R2a、R2b、R2c、R3a、R3b、R4a、R4b、R4c和ml如本文所述。这些化合物可以制备为药物组合物,并可用于预防和治疗包括人类在内的哺乳动物的各种疾病,例如消瘦、骨质疏松症、肌肉减少、性欲下降和/或性功能障碍。
  • NOVEL IMIDAZOLIDINE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS
    申请人:Nique François
    公开号:US20100113547A1
    公开(公告)日:2010-05-06
    Novel compounds are disclosed that have a Formula represented by the following: wherein X, R 1 , R 2a , R 2b , R 2c , R 3a R 3b , R 4a , R 4b , R 4c , and m1 are as described herein. The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, cachexia, osteoporosis, sarcopenia, a decline in libido and/or sexual dysfunction.
    披露了一种具有以下式子表示的新型化合物:其中X、R1、R2a、R2b、R2c、R3aR3b、R4a、R4b、R4c和m1如本文所述。这些化合物可以制备为药物组成物,并可用于预防和治疗哺乳动物包括人类的各种疾病,包括但不限于消瘦症、骨质疏松症、肌肉萎缩症、性欲下降和/或性功能障碍。
  • Imidazolidine compounds as androgen receptor modulators
    申请人:Galapagos NV
    公开号:US07968581B2
    公开(公告)日:2011-06-28
    Novel compounds are disclosed that have a Formula represented by the following: wherein X, R1, R2a, R2b, R2c, R3a R3b, R4a, R4b, R4c, and m1 are as described herein. The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, cachexia, osteoporosis, sarcopenia, a decline in libido and/or sexual dysfunction.
    披露了具有以下公式表示的新化合物:其中X、R1、R2a、R2b、R2c、R3a、R3b、R4a、R4b、R4c和m1的描述如本文所述。这些化合物可以制备成药物组合物,并可用于预防和治疗哺乳动物,包括人类的各种疾病,例如消瘦症、骨质疏松症、肌肉萎缩症、性欲下降和/或性功能障碍等。
  • US7968581B2
    申请人:——
    公开号:US7968581B2
    公开(公告)日:2011-06-28
  • US8383608B2
    申请人:——
    公开号:US8383608B2
    公开(公告)日:2013-02-26
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