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N-Butyl-4-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide | 847023-82-9

中文名称
——
中文别名
——
英文名称
N-Butyl-4-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide
英文别名
1-[5-(Butylsulfamoyl)-2-methoxyphenyl]-3-[4-[6-(morpholin-4-ylmethyl)pyridin-3-yl]naphthalen-1-yl]urea
N-Butyl-4-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide化学式
CAS
847023-82-9
化学式
C32H37N5O5S
mdl
——
分子量
603.742
InChiKey
VAZOYARPRLVOKK-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
  • 重原子数:
    43
  • 可旋转键数:
    11
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    130
  • 氢给体数:
    3
  • 氢受体数:
    8

文献信息

  • [EN] THERAPEUTIC COMPOUNDS AND COMPOSITIONS<br/>[FR] COMPOSÉS ET COMPOSITIONS THÉRAPEUTIQUES
    申请人:AGIOS PHARMACEUTICALS INC
    公开号:WO2014062511A1
    公开(公告)日:2014-04-24
    Provided are aryl sulfonamide diarylurea derivative compounds that are inhibitors of mutant isocitrate dehydrogenase 1/2 (IDH 1/2), useful for treating cancer. Also provided are methods of treating cancer comprising administering to a subject in need thereof a compound described herein. Cancers that are treatable by the compounds of the invention are glioblastoma, myelodysplastic syndrome, myeloproliferative neoplasm, acute myelogenous leukemia, sarcoma, melanoma, non-small cell lung cancer, chondrosarcoma, and non-Hodgkin's lymphoma (NHL).
    提供的是芳基磺酰胺二芳基生物化合物,它们是突变异柠檬酸脱氢酶1/2(IDH 1/2)的抑制剂,可用于治疗癌症。还提供了治疗癌症的方法,包括向需要的受试者施用本文描述的化合物。本发明的化合物可用于治疗的癌症包括胶质母细胞瘤、骨髓增生异常综合征、骨髓增生性肿瘤、急性髓系白血病、肉瘤、黑色素瘤、非小细胞肺癌、软骨肉瘤和非霍奇淋巴瘤(NHL)。
  • Anticoagulant and fibrinolytic therapy uning p38 MAP kinase inhibitors
    申请人:Boehringer Ingelheim Pharmaceuticals, Inc.
    公开号:US20040033222A1
    公开(公告)日:2004-02-19
    Disclosed are methods for a treating a disease or condition relating to blood coagulation and fibrinolysis using p38 MAP kinase inhibitors.
    揭示了利用p38 MAP激酶抑制剂治疗与血液凝血和纤溶有关的疾病或症状的方法。
  • Method of treating mucus hypersecretion
    申请人:Boehringer Ingelheim Pharma GmbH & Co. KG
    公开号:US20030220336A1
    公开(公告)日:2003-11-27
    The invention relates to the use of p38 kinase inhibitors for the preparation of a pharmaceutical composition suitable for inhalation for the treatment of mucus hypersecretion. Furthermore the invention is directed to pharmaceutical compositions suitable for inhalation comprising p38 kinase inhibitors and to methods for the preparation thereof.
    本发明涉及使用p38激酶抑制剂制备适用于治疗黏液过度分泌的吸入药物组合物。此外,本发明还涉及适用于吸入的含有p38激酶抑制剂的药物组合物以及其制备方法。
  • Methods of treating cytokine mediated diseases
    申请人:Boehringer Ingelheim Pharmaceuticals, Inc.
    公开号:US20030060455A1
    公开(公告)日:2003-03-27
    Disclosed are methods of treating acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, sepsis, chronic obstructive pulmonary disease, traumatic arthritis, congestive heart failure and restenosis following percutaneous transluminal coronary angioplasty, known to be cytokine mediated, using aromatic heterocyclic compounds described in WO 00/55139.
    本发明涉及使用在WO 00/55139中描述的芳香族杂环化合物治疗由吸入烟雾、子宫内膜异位症、Behcet病、葡萄膜炎、强直性脊柱炎、胰腺炎、癌症、莱姆病、败血症、慢性阻塞性肺疾病、创伤性关节炎、充血性心力衰竭和经皮冠状动脉成形术后再狭窄等已知为细胞因子介导的急性和慢性肺部炎症治疗的方法。
  • Combination therapy with p38 MAP kinase inhibitors and their pharmaceutical compositions
    申请人:Boehringer Ingelheim Pharmaceuticals, Inc.
    公开号:US20040110755A1
    公开(公告)日:2004-06-10
    The present invention relates to pharmaceutical combinations therapies based on p38 kinase inhibitors and another active ingredient, pharmaceutical compositions comprising such combinations, processes for preparing them and their use in the treatment of cytokine mediated diseases.
    本发明涉及基于p38激酶抑制剂和另一种活性成分的药物组合疗法,包括这种组合物的制药组合物、制备它们的过程以及它们在治疗细胞因子介导的疾病中的应用。
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