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7-bromo-1-(2,6-difluorobenzyl)-1,4-dihydro-6-methyl-4-oxoquinoline-3-carboxylic acid ethyl ester

中文名称
——
中文别名
——
英文名称
7-bromo-1-(2,6-difluorobenzyl)-1,4-dihydro-6-methyl-4-oxoquinoline-3-carboxylic acid ethyl ester
英文别名
1,4-dihydro-l-(2,6-difluorobenzyl)-6-methyl-7-bromo-4-oxoquinoline-3-carboxylic acid ethylester;1,4-dihydro-1-(2,6-difluorobenzyl)-6-methyl-7-bromo-4-oxoquinoline-3-carboxylic acid ethylester;ethyl 7-bromo-1-[(2,6-difluorophenyl)methyl]-6-methyl-4-oxoquinoline-3-carboxylate
7-bromo-1-(2,6-difluorobenzyl)-1,4-dihydro-6-methyl-4-oxoquinoline-3-carboxylic acid ethyl ester化学式
CAS
——
化学式
C20H16BrF2NO3
mdl
——
分子量
436.253
InChiKey
SSOOKSUURPRYEZ-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):
    4.9
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • 7-Heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives useful as antagonists of gonadotropin releasing hormone
    申请人:——
    公开号:US20030216429A1
    公开(公告)日:2003-11-20
    The present invention is directed to novel 7-heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives of the general formula (I) or (II) 1 wherein all variables are as herein defined, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions associated with gonadotropin releasing hormone (GnRH). The compounds of the invention are antagonists of GnRH, useful in the treatment of the infertility, prostate cancer, benign prostate hyperplasia (BPH) and as contraceptives.
    本发明涉及一种新型7-杂环基喹啉噻吩[2,3-b]吡啶衍生物,其通式为(I)或(II)1,其中所有变量如本文所定义,包含它们的药物组合物以及它们在治疗与促性腺激素释放激素(GnRH)相关的疾病和症状中的应用。本发明中的化合物是GnRH拮抗剂,可用于治疗不孕症、前列腺癌、良性前列腺增生(BPH)和避孕。
  • 7-heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives useful as antagonists of gonadotropin releasing hormone
    申请人:Ortho-McNeil Pharmaceutical, Inc.
    公开号:US06765011B2
    公开(公告)日:2004-07-20
    The present invention is directed to novel 7-heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives of the general formula (I) or (II) wherein all variables are as herein defined, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions associated with gonadotropin releasing hormone (GnRH). The compounds of the invention are antagonists of GnRH, useful in the treatment of the infertility, prostate cancer, benign prostate hyperplasia (BPH) and as contraceptives.
    本发明涉及新型的7-杂环基喹啉噻吩[2,3-b]吡啶衍生物,其通式为(I)或(II),其中所有变量均如本文所定义,包含它们的制药组合物以及它们在治疗与促性腺激素释放激素(GnRH)相关的疾病和病症方面的用途。本发明的化合物是GnRH的拮抗剂,可用于治疗不孕症、前列腺癌、良性前列腺增生(BPH)以及避孕。
  • 7-heterocyclyl quinoline and thieno[2,3-b]yridine derivatives useful as antagonists of gonadotropin releasing hormone
    申请人:Ortho-McNeil Pharmaceutical, Inc.
    公开号:US06583153B2
    公开(公告)日:2003-06-24
    The present invention is directed to novel 7-heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives of the general formula (I) or (II) wherein all variables are as herein defined, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions associated with gonadotropin releasing hormone (GnRH). The compounds of the invention are antagonists of GnRH, useful in the treatment of the infertility, prostate cancer, benign prostate hyperplasia (BPH) and as contraceptives.
    本发明涉及一种新型的7-杂环基喹啉噻吩[2,3-b]吡啶衍生物,其通式为(I)或(II),其中所有变量如本文所定义,包含它们的制药组合物以及它们在治疗与促性腺激素释放激素(GnRH)相关的疾病和病况中的应用。本发明的化合物是GnRH拮抗剂,在治疗不孕症、前列腺癌、良性前列腺增生(BPH)和作为避孕药物方面有用。
  • Prolactin production inhibitory agents
    申请人:TAKEDA CHEMICAL INDUSTRIES, LTD.
    公开号:EP0781774A2
    公开(公告)日:1997-07-02
    The prolactin production inhibition agent of the present invention containing a condensed cyclic compound, which is characterized by containing a condensed bicyclic structure of an optionally substituted homo or hetero 5- to 7-membered ring with an optionally substituted homo or hetero 5- to 7-membered ring, or a salt thereof, can be used, as a medicine, for the prophylaxis or therapy of diseases accompanied with an excess prolactin production or diseases having enhanced reactivity with prolactin, or is useful for inhibiting puerperal lactation, and also useful as a prophylactic or therapeutic agent of galactorrhea, hyperprolactinemic ovulation disturbance, amenorrheagalactorrhea syndrome, prolactinoma, and besides, interbrain tumor, and acromegaly, pituitary gigantism.
    本发明的催乳素分泌抑制剂含有缩合环状化合物,其特征在于该化合物含有一个由任选取代的同族或杂族 5 至 7 元环与一个任选取代的同族或杂族 5 至 7 元环组成的缩合双环结构,或其盐,可用作药物、可用于预防或治疗伴有催乳素分泌过多的疾病或与催乳素反应性增强的疾病,也可用于抑制产褥期泌乳,还可用作半乳糖性闭经、高催乳素血症排卵障碍、闭经滞乳综合征、催乳素瘤的预防或治疗药物,此外还可用于脑间肿瘤、肢端肥大症、垂体巨大症。
  • Thieno(2,3-b)pyridine derivatives useful as antagonists of gonadotropin releasing hormone
    申请人:Ortho-McNeil Pharmaceutical, Inc.
    公开号:EP1520855A1
    公开(公告)日:2005-04-06
    The present invention is directed to novel 7-heterocyclyl quinoline and thieno[2,3-b]pyridine derivatives of the general formula (I) or (II), wherein all variables are as herein defined, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions associated with gonadotropin releasing hormone (GnRH). The compounds of the invention are antagonists of GnRH, useful in the treatment of the infertility, prostate cancer, benign prostate hyperplasia (BPH) and as contraceptives.
    本发明涉及通式(I)或(II)的新型 7-杂环喹啉噻吩并[2,3-b]吡啶衍生物(其中所有变量均如本文所定义)、含有它们的药物组合物以及它们在治疗与促性腺激素释放激素(GnRH)相关的疾病和病症中的用途。本发明的化合物是 GnRH 的拮抗剂,可用于治疗不孕症、前列腺癌、良性前列腺增生症(BPH)和避孕。
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