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

UCL 1390 | 152030-48-3

中文名称
——
中文别名
——
英文名称
UCL 1390
英文别名
4-[3-(4-Cyanophenoxy)propyl]-1H-imidazole;4-[3-(1H-Imidazol-4-yl)propoxy]benzonitrile;4-[3-(1H-imidazol-5-yl)propoxy]benzonitrile
UCL 1390化学式
CAS
152030-48-3
化学式
C13H13N3O
mdl
——
分子量
227.266
InChiKey
XQNBJFUWFIHAMW-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

物化性质

  • 沸点:
    505.9±35.0 °C(Predicted)
  • 密度:
    1.20±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    61.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    UCL 1390盐酸羟胺sodium carbonate 作用下, 以 乙醇 为溶剂, 反应 24.0h, 生成 N-hydroxy-4-(3-(1H-imidazol-4-yl)propyloxy)benzamidine oxime
    参考文献:
    名称:
    proxifan系列的新组胺H(3)-受体配体:imoproxifan和其他具有高口服体内效力的选择性拮抗剂。
    摘要:
    描述了proxifan系列的组胺H(3)-受体拮抗剂。该新型化合物具有4-(3-(苯氧基)丙基)-1H-咪唑结构和在苯环上的各种官能团,例如肟部分。描述了新型化合物的合成和一种名为imoproxifan(4-(3-(1H-咪唑-4-基)丙氧基)苯乙酮肟)的高效肟衍生物的X射线晶体学。大多数标题化合物在体内以及在口服给药后的小鼠CNS体内在组胺H(3)-受体测定中均具有很高的拮抗剂效力。讨论了构效关系。在对大鼠大脑皮层突触小体的功能测定中,Imoproxifan表现出亚纳摩尔效价(K(i)= 0.26 nM)。在体内,莫洛昔芬以0.034 mg / kg po的ED(50)升高中心N(tau)-甲基组胺水平。
    DOI:
    10.1021/jm000971p
  • 作为产物:
    描述:
    3-(1-H-imidazol-4-yl)propanol盐酸三乙胺三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 11.0h, 生成 UCL 1390
    参考文献:
    名称:
    一种新型的(苯氧基烷基)咪唑类作为有效的H3受体组胺拮抗剂。
    摘要:
    先前描述的[[(5-硝基吡啶-2-基)X]乙基]咪唑的[[((4-硝基苯基)X]烷基]咪唑等排异构体(其中X = NH,S,CH2S,O)(其中X = NH,已经合成了S),并在体外(对于从大鼠脑皮质突触体释放[3H]组胺的Ki)和在体内(对小鼠脑内远程甲基组胺水平而言,口服ED 50)评估了H3-受体组胺的拮抗作用。令人鼓舞的结果导致合成和测试了一系列新的取代的(苯氧乙基)-和(苯氧丙基)咪唑。后者是4- [3-(4-氰基苯氧基)丙基] -1H-咪唑(10a,UCL 1390; Ki = 12 nM,ED50 = 0.54 mg / kg)和4- [3- [4-(三氟甲基) -苯氧基]丙基] -1H-咪唑(10c,UCL 1409; Ki = 14 nM,ED50 = 0.60 mg / kg)已被选作药物开发的潜在候选药物。
    DOI:
    10.1021/jm960138l
点击查看最新优质反应信息

文献信息

  • AMINOTHIAZOLONES AS ESTROGEN RELATED RECEPTOR-ALPHA MODULATORS
    申请人:Bignan Gilles
    公开号:US20110200587A1
    公开(公告)日:2011-08-18
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎、动脉粥样硬化、关节炎(如类风湿关节炎、感染性关节炎、儿童关节炎、屑病性关节炎、反应性关节炎)、与骨相关的疾病(包括与骨形成有关的疾病)、乳腺癌(包括对抗雌激素治疗无效的癌症)、心血管疾病、软骨相关疾病(如软骨损伤/丧失、软骨退化以及与软骨形成有关的疾病)、软骨发育不全、软骨肉瘤、慢性背部损伤、慢性支气管炎、慢性炎症性气道疾病、慢性阻塞性肺病、糖尿病、能量稳态紊乱、痛风、假性痛风、脂质紊乱、代谢综合征、多发性骨髓瘤、肥胖、骨关节炎、遗传性骨发育不全、骨溶解性骨转移、软骨软化症、骨质疏松症、帕森病、牙周病、多肌痛风、Reiter综合征、重复性应激损伤、高血糖、血糖平升高和胰岛素抵抗等疾病的方法。
  • SUBSTITUTED AMINOTHIAZOLONE INDAZOLES AS ESTROGEN RELATED RECEPTOR-ALPHA MODULATORS
    申请人:BIGNAN Gilles
    公开号:US20110150864A1
    公开(公告)日:2011-06-23
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    该发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎、动脉粥样硬化、关节炎(如类风湿性关节炎、感染性关节炎、儿童关节炎、屑病性关节炎、反应性关节炎)、与骨相关的疾病(包括与骨形成有关的疾病)、乳腺癌(包括对抗雌激素治疗无效的癌症)、心血管疾病、软骨相关疾病(如软骨损伤/丧失、软骨退化以及与软骨形成有关的疾病)、软骨发育不良、软骨肉瘤、慢性腰部损伤、慢性支气管炎、慢性炎症性气道疾病、慢性阻塞性肺疾病、糖尿病、能量稳态紊乱、痛风、假性痛风、脂质紊乱、代谢综合征、多发性骨髓瘤、肥胖、骨关节炎、遗传性骨发育不全、骨转移性溶骨性转移、软骨软化症、骨质疏松症、帕森病、牙周病、多肌痛风、Reiter综合征、重复性应激损伤、高血糖、血糖平升高和胰岛素抵抗等疾病的条件。
  • SUBSTITUTED THIAZOLIDINEDIONE INDAZOLES, INDOLES AND BENZOTRIAZOLES AS ESTROGEN-RELATED RECEPTOR-a MODULATORS
    申请人:Bignan Gilles
    公开号:US20110294780A1
    公开(公告)日:2011-12-01
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎,动脉粥样硬化,关节炎(如类风湿关节炎,感染性关节炎,儿童关节炎,屑病性关节炎,反应性关节炎),与骨相关的疾病(包括与骨形成有关的疾病),乳腺癌(包括对抗雌激素治疗无效的癌症),心血管疾病,软骨相关疾病(如软骨损伤/丧失,软骨退化以及与软骨形成有关的疾病),软骨发育不良,软骨肉瘤,慢性腰部损伤,慢性支气管炎,慢性炎症性气道疾病,慢性阻塞性肺疾病,糖尿病,能量稳态紊乱,痛风,假性痛风,脂质紊乱,代谢综合征,多发性骨髓瘤,肥胖,骨关节炎,遗传性骨发育不全,骨溶解性骨转移,软骨软化症,骨质疏松症,帕森病,牙周病,多肌痛风,Reiter综合征,重复性应激损伤,高血糖,血糖平升高和胰岛素抵抗等病症的方法。
  • SUBSTITUTED PHENOXY N-ALKYLATED THIAZOLIDINEDIONES AS ESTROGEN RELATED RECEPTOR-ALPHA MODULATORS
    申请人:Gaul Michael
    公开号:US20080286265A1
    公开(公告)日:2008-11-20
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及化合物的公式(I),制备这些化合物的方法,组合物,中间体及其衍生物,用于治疗包括但不限于强直性脊柱炎,动脉粥样硬化,关节炎(如类风湿性关节炎,感染性关节炎,儿童关节炎,屑病性关节炎,反应性关节炎),与骨相关的疾病(包括与骨形成有关的疾病),乳腺癌(包括对抗雌激素治疗无效的癌症),心血管疾病,软骨相关疾病(如软骨损伤/丧失,软骨退化,以及与软骨形成有关的疾病),软骨发育不全,软骨肉瘤,慢性背部损伤,慢性支气管炎,慢性炎症性气道疾病,慢性阻塞性肺病,糖尿病,能量稳态紊乱,痛风,假性痛风,脂质紊乱,代谢综合征,多发性骨髓瘤,肥胖,骨关节炎,成骨不全症,骨溶解性骨转移,软骨软化症,骨质疏松症,Paget病,牙周病,多肌痛风,Reiter综合征,重复性应激损伤,高血糖,血糖平升高和胰岛素抵抗等病症的条件。
  • SUBSTITUTED PHENOXY AMINOTHIAZOLONES as estrogen related receptor-alpha modulators
    申请人:Gaul Michael
    公开号:US20080221179A1
    公开(公告)日:2008-09-11
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎,动脉粥样硬化,关节炎(如类风湿性关节炎,感染性关节炎,儿童关节炎,屑病性关节炎,反应性关节炎),与骨相关的疾病(包括与骨形成有关的疾病),乳腺癌(包括对抗雌激素治疗无效的癌症),心血管疾病,软骨相关疾病(如软骨损伤/缺失,软骨退变以及与软骨形成有关的疾病),软骨发育不良,软骨肉瘤,慢性背部损伤,慢性支气管炎,慢性炎性气道疾病,慢性阻塞性肺疾病,糖尿病,能量稳态紊乱,痛风,假性痛风,脂质紊乱,代谢综合征,多发性骨髓瘤,肥胖,骨关节炎,成骨不全症,骨转移性溶骨病,软骨软化症,骨质疏松症,帕森病,牙周病,多肌痛风,Reiter综合征,重复性应力损伤,高血糖,血糖平升高以及胰岛素抵抗等情况的治疗。
查看更多

同类化合物

(R)-3-(叔丁基)-4-(2,6-二异丙氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2R,2''R,3R,3''R)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2-氟-3-异丙氧基苯基)三氟硼酸钾 (+)-6,6'-{[(1R,3R)-1,3-二甲基-1,3基]双(氧)}双[4,8-双(叔丁基)-2,10-二甲氧基-丙二醇 麦角甾烷-6-酮,2,3,22,23-四羟基-,(2a,3a,5a,22S,23S)- 鲁前列醇 顺式6-(对甲氧基苯基)-5-己烯酸 顺式-铂戊脒碘化物 顺式-四氢-2-苯氧基-N,N,N-三甲基-2H-吡喃-3-铵碘化物 顺式-4-甲氧基苯基1-丙烯基醚 顺式-2,4,5-三甲氧基-1-丙烯基苯 顺式-1,3-二甲基-4-苯基-2-氮杂环丁酮 非那西丁杂质7 非那西丁杂质3 非那西丁杂质22 非那西丁杂质18 非那卡因 非布司他杂质37 非布司他杂质30 非布丙醇 雷诺嗪 阿达洛尔 阿达洛尔 阿莫噁酮 阿莫兰特 阿维西利 阿索卡诺 阿米维林 阿立酮 阿曲汀中间体3 阿普洛尔 阿普斯特杂质67 阿普斯特中间体 阿普斯特中间体 阿托西汀EP杂质A 阿托莫西汀杂质24 阿托莫西汀杂质10 阿托莫西汀EP杂质C 阿尼扎芬 阿利克仑中间体3 间苯胺氢氟乙酰氯 间苯二酚二缩水甘油醚 间苯二酚二异丙醇醚 间苯二酚二(2-羟乙基)醚 间苄氧基苯乙醇 间甲苯氧基乙酸肼 间甲苯氧基乙腈 间甲苯异氰酸酯