摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-((R,R)-octahydropyrrolo[3,4-b]pyridin-6-yl)-8,8-difluoro-6,7,8,9-tetrahydro[1]benzofuro[3,2-d]pyrimidin-2-amine | 1132689-99-6

中文名称
——
中文别名
——
英文名称
4-((R,R)-octahydropyrrolo[3,4-b]pyridin-6-yl)-8,8-difluoro-6,7,8,9-tetrahydro[1]benzofuro[3,2-d]pyrimidin-2-amine
英文别名
4-[(4aR,7aR)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-8,8-difluoro-7,9-dihydro-6H-[1]benzofuro[3,2-d]pyrimidin-2-amine
4-((R,R)-octahydropyrrolo[3,4-b]pyridin-6-yl)-8,8-difluoro-6,7,8,9-tetrahydro[1]benzofuro[3,2-d]pyrimidin-2-amine化学式
CAS
1132689-99-6
化学式
C17H21F2N5O
mdl
——
分子量
349.383
InChiKey
HJGYVEWDFYLBCZ-KOLCDFICSA-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):
    2.3
  • 重原子数:
    25
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    80.2
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • Thieno-and furo-pyrimidine modulators of the histamine H4 receptor
    申请人:Edwards James P.
    公开号:US20090075970A1
    公开(公告)日:2009-03-19
    Thieno- and furo-pyrimidine compounds are described, which are useful as H 4 receptor modulators. Such compounds may be used in pharmaceutical compositions and methods for the modulation of histamine H 4 receptor activity and for the treatment of disease states, disorders, and conditions mediated by H 4 receptor activity, such as inflammation.
    描述了噻吩-和呋喃-嘧啶化合物,这些化合物可用作H4受体调节剂。这些化合物可以用于制药组合物和用于调节组胺H4受体活性以及治疗由H4受体活性介导的疾病状态、紊乱和条件的方法,如炎症。
  • Selective Histamine H4 Receptor Antagonists for the Treatment of Vestibular Disorders
    申请人:Desmadryl Gilles
    公开号:US20120039913A1
    公开(公告)日:2012-02-16
    The invention relates to Histamine H4 receptor antagonists or inhibitors of Histamine H4 receptor gene expression for the treatment and/or the prevention of vestibular disorders.
    该发明涉及组胺H4受体拮抗剂或组胺H4受体基因表达抑制剂,用于治疗和/或预防前庭障碍。
  • THIENO- AND FURO-PYRIMIDINE MODULATORS OF THE HISTAMINE H4 RECEPTOR
    申请人:Edwards James P.
    公开号:US20120270855A1
    公开(公告)日:2012-10-25
    Thieno- and furo-pyrimidine compounds are described, which are useful as H 4 receptor modulators. Such compounds may be used in pharmaceutical compositions and methods for the modulation of histamine H 4 receptor activity and for the treatment of disease states, disorders, and conditions mediated by H 4 receptor activity, such as inflammation.
    本文描述了一种噻吩呋喃嘧啶化合物,可用作H4受体调节剂。这些化合物可用于制备药物组合物和方法,用于调节组胺H4受体活性和治疗由H4受体活性介导的疾病状态、障碍和病况,如炎症。
  • THIENO- ADN FURO-PYRIMIDINE MODULATORS OF THE HISTAMINE H4 RECEPTOR
    申请人:Edwards James P.
    公开号:US20120214792A1
    公开(公告)日:2012-08-23
    Thieno- and furo-pyrimidine compounds are described, which are useful as H 4 receptor modulators. Such compounds may be used in pharmaceutical compositions and methods for the modulation of histamine H 4 receptor activity and for the treatment of disease states, disorders, and conditions mediated by H 4 receptor activity, such as inflammation.
    本文描述了噻吩呋喃嘧啶化合物,可用作H4受体调节剂。这些化合物可用于制备药物组合物和方法,以调节组胺H4受体活性,并用于治疗由H4受体活性介导的疾病状态、障碍和病情,例如炎症。
  • SELECTIVE HISTAMINE H4 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF VESTIBULAR DISORDERS
    申请人:INSERM (Institut National de la Santé et de la Recherche Médicale)
    公开号:EP3130376A1
    公开(公告)日:2017-02-15
    The invention relates to Histamine H4 receptor antagonists or inhibitors of Histamine H4 receptor gene expression for the treatment and/or the prevention of vestibular disorders.
    本发明涉及组胺 H4 受体拮抗剂或组胺 H4 受体基因表达抑制剂,用于治疗和/或预防前庭失调。
查看更多

同类化合物

锯齿石松宁 脱氧卡色素B 箭毒蛙毒素 C 环戊二烯并[b]吖庚英-5-醇,十氢- 坎库碘铵 十氢喹啉 十氢-2-甲基喹啉 八氢对苯二酚-4(1H)-酮 八氢喹啉-2(1H)-酮 八氢-2,6-喹啉二酮 二氯化硅2,3-萘醛菁 β-羟基丙基-环糊精 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-二甲基-1,2,3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十六氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-1,10a,12a-三甲基-2-氧代-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 8H-13,3,6a-乙基亚基-7,10-亚甲基噁庚并[3,4-i]-1-苯并吖辛因-8-酮,1-乙基十四氢-12a-羟基-6-甲氧基-3-甲基-,(3R,6S,6aS,7R,7aS,10S,12aS,13S,13aR,15R)-(9CI) 8-羟基-十氢喹啉 4-乙炔基-2-甲基十氢喹啉-4-醇 4-乙炔基-2-甲基-1-(3-苯丙-2-炔-1-基)十氢喹啉-4-醇 3-羟基-13,17-开环-5-雄甾烯-17-酸-13,17-内酰胺(4-(二(2-氯乙基)氨基)苯基)丁酸酯 3-甲氧基-17-氮杂-高雄甾-5-烯-17-酮 2H-环戊二烯并[b]吡啶-2-酮,八氢-4-甲基-,[4S-(4-α-,4a-bta-,7a-bta-)]-(9CI) 2-甲基-1-(3-丙氧基-丙基)-八氢-喹啉-4-酮 2,5-二丙基十氢喹啉 1-(3-甲氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1-(3-氯-丙基)-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1,2,2-三甲基-八氢-喹啉-4-酮 (4aS,4bR,8S,10aR,10bS,12aS)-10a,12a-二甲基-2-羰基-1,2,3,4,4a,4b,5,7,8,9,10,10a,10b,11,12,12a-十六氢萘并[2,1-f]喹啉-8-基{4-[二(2-氯乙基)氨基]苯基}乙酸酯 (4aS,4bR,6aS,8S,10aS,10bS,12aS)-8-羟基-10a,12a-二甲基-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢-1H-萘并[2,1-f]喹啉-2-酮 (3S,13R)-1,2,3,4,4aalpha,5,11,11aalpha-八氢-2,2,5-三甲基-3beta,5beta-乙桥-10bH-吡啶并[3,2-b]咔唑-10bbeta,13-二醇 (3R,6S,6aS,7R,7aS,10S,12aS,13R,13aR,14S,15R)-1-乙基十四氢-12a,14-二羟基-6-甲氧基-3-甲基-8H-13,3,6a-亚乙基-7,10-甲桥氧杂卓并[3,4-i]-1-苯并氮杂环辛四烯-8-酮 (2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮 (2R,4R,4As,8As)-rel-4-乙炔基十氢-1,2-二甲基-4-喹啉醇 1-(2-Cyclopentylethyl)-perhydrochinolin Perhydrodibenzochinolizin octahydroquinoline-1(2H)-carbonitrile N-Acetylbaikeidin 4-[4-[(4aR,8aR)-3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carbonyl]thiophen-2-yl]piperidine-1-carboxamide N-Chlor-trans-decahydrochinolin (4aR,8aR)-1-{4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidin-1-yl}-ethanone (7-Acetyl-3a,6-dimethyl-3-oxo-tetradecahydro-7-aza-cyclohepta[e]inden-6-yl)-acetic acid 6,7-Cyclobutano-1,2-cyclopropano-chinolizidin 2-Methyl-2,3-tetramethylen-N-cyanoaziridin (4aR)-2-oxo-1-[(1R)-1-phenylethyl]-4,5,6,7-tetrahydro-3H-quinoline-4a-carboxylic acid (4aR,8aR)-(octahydro-quinolin-1(2H)-yl)-(5-piperidin-4-yl-thiophen-3-yl)-methanone 5-(octahydroquinolin-1-yl)-5-oxopentanoic acid N-benzyl-N-isopropylamide 3,4,4-Trimethyl-2-azabicyclo<3.3.0>octan (4aR,8aR)-4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidine-1-carboxylic acid tert-butyl ester 1-Aza-4,11-dioxo-3-oxo-methoxycarbonyl-tricyclo<5.3.1.05,10>undecan