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compound 29 | 1055361-35-7

中文名称
——
中文别名
——
英文名称
compound 29
英文别名
4-[4-(2,4-dioxothiazolidin-5-ylidenemethyl)-2-methoxyphenoxy]-3-trifluoromethylbenzonitrile;4-[4-(2,4-Dioxo-thiazolidin-5-ylidenemethyl)-2-methoxy-phenoxy]-3-trifluoromethyl-benzonitrile;4-[4-[(2,4-dioxo-1,3-thiazolidin-5-ylidene)methyl]-2-methoxyphenoxy]-3-(trifluoromethyl)benzonitrile
compound 29化学式
CAS
1055361-35-7
化学式
C19H11F3N2O4S
mdl
——
分子量
420.369
InChiKey
OBBIOCQFTMNSJI-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):
    4.3
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    9

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:
    compound 29偶氮二甲酸二异丙酯三苯基膦三氟乙酸 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 6.0h, 生成
    参考文献:
    名称:
    荧光探针化合物及其制备方法和应用
    摘要:
    本发明涉及生物分析领域,公开了一种荧光探针化合物及其制备方法和应用。一类荧光探针化合物,具有式(I)所示的结构,其中R为具有与氨基反应活性的有机荧光分子基团;本发明还提供了式(I)所示的荧光探针化合物的制备方法,包括以下步骤:在反应溶剂I和催化剂I存在的条件下,将式(II)所示的化合物和具有与氨基反应活性的有机荧光分子进行反应I;本发明提供的荧光探针化合物可有效检测待测样品与ERRα的结合能力,且准确性高、操作简单,可用于高通量快速筛查;
    公开号:
    CN113788830B
  • 作为产物:
    描述:
    4-氟-3-三氟甲基苯腈sodium acetatepotassium carbonate 作用下, 以 N,N-二甲基甲酰胺乙腈 为溶剂, 反应 24.0h, 生成 compound 29
    参考文献:
    名称:
    荧光探针化合物及其制备方法和应用
    摘要:
    本发明涉及生物分析领域,公开了一种荧光探针化合物及其制备方法和应用。一类荧光探针化合物,具有式(I)所示的结构,其中R为具有与氨基反应活性的有机荧光分子基团;本发明还提供了式(I)所示的荧光探针化合物的制备方法,包括以下步骤:在反应溶剂I和催化剂I存在的条件下,将式(II)所示的化合物和具有与氨基反应活性的有机荧光分子进行反应I;本发明提供的荧光探针化合物可有效检测待测样品与ERRα的结合能力,且准确性高、操作简单,可用于高通量快速筛查;
    公开号:
    CN113788830B
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文献信息

  • 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.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体和衍生物以及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,银屑病性关节炎,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乳腺癌),心血管疾病,软骨相关疾病(如软骨损伤/丧失,软骨退化和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,能量稳态紊乱疾病,痛风,假性痛风,脂质代谢紊乱,代谢综合症,多发性骨髓瘤,肥胖症,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,帕吉特病,牙周疾病,多肌病性风湿病,Reiter综合症,反复应力损伤,高血糖,血糖水平升高和胰岛素抵抗等疾病的治疗。
  • Substituted phenoxy N-alkylated thiazolidinediones as estrogen related receptor-α modulators
    申请人:Janssen Pharmaceutica N.V.
    公开号:US08119669B2
    公开(公告)日:2012-02-21
    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)化合物、制备这些化合物的方法、组合物、中间体和衍生物以及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、银屑病性关节炎、反应性关节炎)、与骨形成有关的骨相关疾病、乳腺癌(包括对抗雌激素治疗无效的乳腺癌)、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、能量稳态紊乱疾病、痛风、假性痛风、脂质代谢紊乱、代谢综合征、多发性骨髓瘤、肥胖症、骨关节炎、成骨不全症、骨转移性溶解、佝偻病、骨质疏松症、帕吉特病、牙周病、多肌病性风湿痛、Reiter综合征、重复性应力损伤、高血糖、血糖升高水平和胰岛素抵抗等疾病的治疗。
  • Identification of Diaryl Ether-Based Ligands for Estrogen-Related Receptor α as Potential Antidiabetic Agents
    作者:Raymond J. Patch、Lily L. Searle、Alexander J. Kim、Debyendu De、Xizhen Zhu、Hossein B. Askari、John C. O’Neill、Marta C. Abad、Dionisios Rentzeperis、Jianying Liu、Michael Kemmerer、Ling Lin、Jyotsna Kasturi、John G. Geisler、James M. Lenhard、Mark R. Player、Micheal D. Gaul
    DOI:10.1021/jm101063h
    日期:2011.2.10
    Estrogen-related receptor a (ERR alpha) is an orphan nuclear receptor that has been functionally implicated in the regulation of energy homeostasis. Herein is described the development of diaryl ether based thiazolidenediones, which function as selective ligands against this receptor. Series optimization provided several potent analogues that inhibit the recruitment of a coactivator peptide fragment in in vitro biochemical assays (IC50 < 150 nM) and cellular two-hybrid reporter assays against the ligand binding domain (IC50 = 1-5 mu M). A cocrystal structure of the ligand-binding domain of ERR alpha with lead compound 29 revealed the presence of a covalent interaction between the protein and ligand, which has been shown to be reversible. In diet-induced murine models of obesity and in an overt diabetic rat model, oral administration of 29 normalized insulin and circulating triglyceride levels, improved insulin sensitivity, and was body weight neutral. This provides the first demonstration of functional activities of an ERRa ligand in metabolic animal models.
  • 荧光探针化合物及其制备方法和应用
    申请人:湖南农业大学
    公开号:CN113788830B
    公开(公告)日:2022-08-09
    本发明涉及生物分析领域,公开了一种荧光探针化合物及其制备方法和应用。一类荧光探针化合物,具有式(I)所示的结构,其中R为具有与氨基反应活性的有机荧光分子基团;本发明还提供了式(I)所示的荧光探针化合物的制备方法,包括以下步骤:在反应溶剂I和催化剂I存在的条件下,将式(II)所示的化合物和具有与氨基反应活性的有机荧光分子进行反应I;本发明提供的荧光探针化合物可有效检测待测样品与ERRα的结合能力,且准确性高、操作简单,可用于高通量快速筛查;
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