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9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-N-{2-[(([2-(1-piperidinyl)ethyl]amino}carbonyl)amino]ethyl}-9H-purine-2-carboxamide | 380221-58-9

中文名称
——
中文别名
——
英文名称
9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-N-{2-[(([2-(1-piperidinyl)ethyl]amino}carbonyl)amino]ethyl}-9H-purine-2-carboxamide
英文别名
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-(2,2-diphenylethylamino)-N-[2-(2-piperidin-1-ylethylcarbamoylamino)ethyl]purine-2-carboxamide
9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-N-{2-[(([2-(1-piperidinyl)ethyl]amino}carbonyl)amino]ethyl}-9H-purine-2-carboxamide化学式
CAS
380221-58-9
化学式
C35H45N9O6
mdl
——
分子量
687.799
InChiKey
VXPZAYJMFOBPQZ-ZLXUNRMYSA-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):
    1.8
  • 重原子数:
    50
  • 可旋转键数:
    14
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    199
  • 氢给体数:
    7
  • 氢受体数:
    11

反应信息

  • 作为产物:
    描述:
    N-(2-Aminoethyl)-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purine-2-carboxamide 、 N-[2-(1-Piperidinyl)ethyl]-1H-imidazole-1-carboxamide 在 silica gel 、 二氯甲烷乙醚 作用下, 以 甲苯异丙醇 为溶剂, 反应 4.0h, 以to afford the title compound as a white powder (85 mg)的产率得到9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-N-{2-[(([2-(1-piperidinyl)ethyl]amino}carbonyl)amino]ethyl}-9H-purine-2-carboxamide
    参考文献:
    名称:
    2-Aminocarbonyl-9H-purine derivatives
    摘要:
    本发明涉及以下式的化合物:及其药学上可接受的盐和溶剂,以及制备该化合物的中间体,包含该化合物的组合物的制备方法和用途。
    公开号:
    US20060122145A1
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文献信息

  • Combination therapies
    申请人:Pfizer Inc
    公开号:US20040209916A1
    公开(公告)日:2004-10-21
    The invention is directed to methods of treating asthma, COPD, allergic rhinitis, and infectious rhinitis by administering a first pharmaceutical agent including one or more compounds selected from the quarternary ammonium compounds of formulae I-V and a second pharmaceutical agent including one or more pharmaceutical agents selected from Adenosine A 2a Receptor Agonists, D2-Dopamine Receptor Agonists, Phosphodiesterase Inhibitors (PDE's), corticosteroids, norepinephrine reuptake inhibitors, 4-hydroxy-7-[2-[2-[3-[2-phenylethoxy]-propylsulphonyl]ethylamino]ethyl]-1,3-benzothiazol-2(3H)-one, and pharmaceutically acceptable salts thereof, and non-quarternized antimuscarinic compounds.
    该发明涉及通过给予包括公式I-V的季化合物中选取的一个或多个化合物以及包括选自腺苷A2a受体激动剂、D2-多巴胺受体激动剂、磷酸二酯酶抑制剂(PDE's)、皮质类固醇去甲肾上腺素再摄取抑制剂4-羟基-7-[2-[2-[3-[2-苯乙氧基]-丙磺酰乙基]-乙基]-1,3-苯并噻唑-2(3H)-酮及其药用可接受的盐以及非季化的抗胆碱药物的第二药物,来治疗哮喘、COPD、过敏性鼻炎和感染性鼻炎的方法。
  • 2-aminocarbonyl-9H-purine derivatives
    申请人:——
    公开号:US20020058641A1
    公开(公告)日:2002-05-16
    The present invention relates to compounds of the formula. 1 and pharmaceutically acceptable salts and solvates thereof, and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such compounds.
    本发明涉及公式.1的化合物及其药学上可接受的盐和溶剂化物,以及制备这些化合物所使用的中间体、含有这些化合物的组合物的制备方法和用途。
  • Combination of an adenosine A2A-receptor agonist and tiotropium or a derivative thereof for treating obstructive airways and other inflammatory diseases
    申请人:Boehringer Ingelheim Pharma KG
    公开号:US20030013675A1
    公开(公告)日:2003-01-16
    A combination of therapeutic agents useful in the treatment of obstructive airways and other inflammatory diseases comprising (i) an adenosine A 2A receptor agonist; and (ii) an anti-cholinergic agent, preferably comprising a member selected from the group consisting of tiotropium and derivatives thereof; the combination being therapeutically effective in the treatment of the diseases when administered by inhalation; as well as to a method of treating the obstructive airways and other inflammatory diseases comprising administering separately, simultaneously or sequentially to the mammal by inhalation a therapeutically effective amount of the combination of therapeutic agents; as well as to a pharmaceutical composition comprising a pharmaceutically acceptable carrier together with the combination of therapeutic agents; as well as to a product containing the compounds of the combination for separate, simultaneous or sequential administration by inhalation to a mammal for the treatment of obstructive airways and other inflammatory diseases. It is preferred that the anti-cholinergic agent component be tiotropium bromide.
    一种用于治疗阻塞性气道和其他炎症性疾病的治疗剂组合,包括(i) 一种腺苷 A 2A 受体激动剂;以及(ii) 抗胆碱能药物,优选包含选自由噻托及其衍生物组成的组中的成员;当通过吸入给药时,该组合对治疗疾病有效;以及治疗阻塞性气道和其他炎症性疾病的方法,包括通过吸入给哺乳动物分别、同时或依次给药治疗有效量的治疗剂组合;以及包含药学上可接受的载体和治疗剂组合物的药物组合物;以及包含组合物化合物的产品,用于通过吸入对哺乳动物单独、同时或连续给药,以治疗阻塞性气道和其他炎症性疾病。抗胆碱能药物成分最好是噻托
  • 2-AMINOCARBONYL-9H-PURINE DERIVATIVES
    申请人:Pfizer Limited
    公开号:EP1292604B1
    公开(公告)日:2009-05-13
  • US6753322B2
    申请人:——
    公开号:US6753322B2
    公开(公告)日:2004-06-22
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