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5-cyclopropyl-7-methoxy-2-(2-(4-morpholinylmethyl)-7,8-dihydro[1,6]naphthyridin-6(5H)-yl)-4(3H)-quinazolinone

中文名称
——
中文别名
——
英文名称
5-cyclopropyl-7-methoxy-2-(2-(4-morpholinylmethyl)-7,8-dihydro[1,6]naphthyridin-6(5H)-yl)-4(3H)-quinazolinone
英文别名
5-cyclopropyl-7-methoxy-2-[2-(morpholin-4-ylmethyl)-7,8-dihydro-5H-1,6-naphthyridin-6-yl]-3H-quinazolin-4-one
5-cyclopropyl-7-methoxy-2-(2-(4-morpholinylmethyl)-7,8-dihydro[1,6]naphthyridin-6(5H)-yl)-4(3H)-quinazolinone化学式
CAS
——
化学式
C25H29N5O3
mdl
——
分子量
447.5
InChiKey
RANRGTUKIYNXAV-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):
    1.6
  • 重原子数:
    33
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    79.3
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    5-cyclopropyl-7-methoxy-2-(2-[(1S,4S)-2-oxa-5-azabicyclo[2.2.1]hept-5-ylmethyl]-7,8-dihydro[1,6]naphthyridin-6(5H)-yl)-4(3H)-quinazolinone 、 5-cyclopropyl-7-methoxy-2-(2-(4-morpholinylmethyl)-7,8-dihydro[1,6]naphthyridin-6(5H)-yl)-4(3H)-quinazolinone 、 生成 5-cyclopropyl-7-methoxy-2-(5-[(1S,4S)-2-oxa-5-azabicyclo[2.2.1]hept-5-ylmethyl]-3,4-dihydro[2,6]naphthyridin-2(1H)-yl)-4(3H)-quinazolinone
    参考文献:
    名称:
    Treatment of female sexual dysfunction
    摘要:
    本发明涉及使用α1A和/或α1L肾上腺素受体拮抗剂治疗女性性功能障碍(FSD),特别是女性性唤起障碍(FSAD)和/或女性性高潮障碍(FOD)。本发明还涉及一种治疗FSD,特别是FSAD和/或FOD的方法,以及用于筛选有用于治疗FSD,特别是FSAD和/或FOD的化合物的测定方法。
    公开号:
    US20040132697A1
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文献信息

  • Compounds Useful In Therapy
    申请人:Gibson Karl Richard
    公开号:US20080096950A1
    公开(公告)日:2008-04-24
    Compounds of Formula (I): and pharmaceutically acceptable salts, solvates (including hydrates) of said compounds and salts, or prodrugs of said compound, or pharmaceutically acceptable salts or solvates of said prodrugs, wherein the substituents are as herein defined, are useful in therapy, for example they may be useful for treating progesterone-mediated conditions such as endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), or chronic pelvic pain syndrome.
    化合物的化学式(I): 以及所述化合物及其盐、溶剂化合物(包括合物)和盐、或所述化合物的前药,或所述前药的药学上可接受的盐或溶剂化合物,其中取代基如本文所定义,可用于治疗,例如它们可能对治疗孕激素介导的疾病如子宫内膜异位症、子宫肌瘤(平滑肌瘤)、月经过多、子宫腺肌病、原发性和继发性痛经(包括性交疼痛、排便疼痛和慢性盆腔疼痛症状)或慢性盆腔疼痛综合症等方面具有用处。
  • Compounds useful in therapy
    申请人:Bradley Anthony Paul
    公开号:US20070105909A1
    公开(公告)日:2007-05-10
    Compounds of formula (I), or a pharmaceutically acceptable derivative thereof, wherein R 1 and R 3 independently represent H, C 1-6 alkyl, C 3-8 cycloalkyl, or halogen; R 2 represents C 1-6 alkyl, CF 3 or aryl; a represents 1 or 2; R 4 , R 5 , R 7 and R 8 independently represent H, C 1-6 alkyl, C 1-6 alkyloxy, CN or halogen, or R 4 and R 5 , or R 7 and R 8 , together with the ring to which they are attached form an aryl or heterocyclic fused ring system; X represents C or N; Y represents CH 2 or O; R 6 represents H, CN or halo provided that, when X represents N, R 6 is absent. The compounds are useful for treating endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), or chronic pelvic pain syndrome.
    式(I)的化合物,或其药学上可接受的衍生物,其中R1和R3独立地代表H、C1-6烷基、C3-8环烷基或卤素;R2代表C1-6烷基、CF3或芳基;a代表1或2;R4、R5、R7和R8独立地代表H、C1-6烷基、C1-6烷氧基、CN或卤素,或R4和R5,或R7和R8,与它们连接的环一起形成芳基或杂环融合环系统;X代表C或N;Y代表CH2或O;R6代表H、CN或卤素,但当X代表N时,R6不存在。这些化合物可用于治疗子宫内膜异位症、子宫肌瘤(平滑肌瘤)、月经过多、子宫腺肌病、原发性和继发性痛经(包括性交疼痛、性交困难和慢性盆腔疼痛症状)或慢性盆腔疼痛综合征。
  • Lactams as tachkinin antagonists
    申请人:Pfizer Inc.
    公开号:US20040132710A1
    公开(公告)日:2004-07-08
    Compounds of the formula (I): 1 or a pharmaceutically acceptable salt, prodrug, solvate or polymorph thereof, wherein R, R 1 , and Z are as defined herein, are useful in treating or preventing a condition for which an NK 2 antagonist is efficacious.
    公式(I)的化合物:1或其药学上可接受的盐,前药,溶剂化合物或多晶形式,其中R,R1和Z的定义如本文所述,可用于治疗或预防NK2拮抗剂有效的疾病。
  • Combinations of atorvastatin and alpha1adrenergic receptor antagonists
    申请人:Pfizer Inc
    公开号:US20040132728A1
    公开(公告)日:2004-07-08
    Combinations of atorvastatin and &agr; 1 adrenergic receptor antagonists, the use of such combinations in the treatment of benign prostatic hyperplasia (BPH), methods of treating BPH using such combinations and medicaments containing such combinations are described.
    本文描述了阿托伐他汀和α1肾上腺素受体拮抗剂的组合,以及在治疗良性前列腺增生症(BPH)中使用此类组合的方法和含有此类组合的药物。
  • 1H-Pyrazoles Useful In Therapy
    申请人:Bradley Anthony Paul
    公开号:US20080085919A1
    公开(公告)日:2008-04-10
    Compounds of formula (I), or a pharmaceutically acceptable derivative thereof, wherein R 1 and R 3 independently represent H, C 1-6 alkyl, C 3-8 cycloalkyl, or halogen; R 2 represents C 1-6 alkyl, CF 3 or aryl; a represents 1 or 2; R 4 , R 5 , R 7 and R 8 independently represent H, C 1-6 alkyl, C 1-6 alkyloxy, CN or halogen, or R 4 and R 5 , or R 7 and R 8 , together with the ring to which they are attached form an aryl or heterocyclic fused ring system; X represents C or N; Y represents CH 2 or O; R 6 represents H, CN or halo provided that, when X represents N, R 6 is absent. The compounds are useful for treating endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), or chronic pelvic pain syndrome.
    化合物的式子(I),或其药学上可接受的衍生物,其中R1和R3独立地表示H,C1-6烷基,C3-8环烷基或卤素; R2表示C1-6烷基,CF3或芳基; a表示1或2; R4,R5,R7和R8独立地表示H,C1-6烷基,C1-6烷氧基,CN或卤素,或者R4和R5,或R7和R8,与它们连接的环共同形成芳基或杂环融合环系统; X表示C或N; Y表示CH2或O; R6表示H,CN或卤素,但当X表示N时,R6不存在。这些化合物可用于治疗子宫内膜异位症,子宫肌瘤(平滑肌瘤),月经过多,子宫内膜增生症,原发性和继发性痛经(包括性交疼痛,排便疼痛和慢性盆腔疼痛症状),或慢性盆腔疼痛综合征。
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